Today's Pharma & Biotech Jobs

Lead strategic and tactical elements of the brand strategy and tactical plan, including value propositions, positioning, segmentation, and creative development. Develop and articulate effective oncology marketing strategies that are impactful, executable, easily communicated, and clinically/financially supported for relevant areas of responsibility (product/indication/channel). Responsibilities Collaborate with Marketing Director(s) and business leaders in the brand team to build, manage, and execute marketing plans to achieve oncology business objectives and goals, including patient, market, and financial results for oncology brands. Drive and participate in business and marketing planning processes specific to oncology. Demonstrate and utilize a holistic understanding of oncology-specific financial planning. Lead...

The Marketing Director will lead U.S. launch readiness for a new asset for Multiple Myeloma. This role will have people management and collectively the team will be responsible for establishing the cross-functional launch team and leading strategy, positioning, messaging, go-to-market, tactical planning to ensure launch success. The candidate should be able to work effectively in a dynamic organization and deliver high-quality work in partnership with internal and external stakeholders to support business objectives. Additionally, the candidate will build and maintain strong working relationships with cross-functional and co-promotion partners to move priorities forward in a thoughtful, collaborative, and timely way. This...

This role can be based anywhere in the United States. The Director, Thought Leader Liaison (TLL) leads a team of Thought Leader Liaisons for Multiple Myeloma in shaping and executing an external expert engagement strategy that advances brand and franchise objectives. This role is responsible for building team capability and accountability, strengthening relationships with national and regional oncology hematology experts, ensuring external perspectives inform leadership and brand decisions, and partnering cross-functionally to deliver compliant, measurable engagement activities that expand and strengthen the thought leader base. Accountabilities include Lead, hire, train, inspire and drive accountability for Thought Leader Liaison team Ensure...

The Marketing Director will lead U.S. launch readiness for a new asset for Multiple Myeloma. This role will have people management and collectively the team will be responsible for establishing the cross-functional launch team and leading strategy, positioning, messaging, go-to-market, tactical planning to ensure launch success. The candidate should be able to work effectively in a dynamic organization and deliver high-quality work in partnership with internal and external stakeholders to support business objectives. Additionally, the candidate will build and maintain strong working relationships with cross-functional and co-promotion partners to move priorities forward in a thoughtful, collaborative, and timely way. This...

Executive Director – Global Market Access & Pricing – Immunology Role Summary Our Immunology portfolio represents a top corporate priority and a key driver of long-term growth, with a robust pipeline of innovative therapies across immune-mediated diseases. The Global Market Access (GMAx) organization plays a critical role in ensuring timely, broad, and sustainable patient access to these innovations at a price reflective of their value. The Executive Director, Global Market Access & Pricing – Immunology is a senior leader responsible for setting and driving the global access, pricing, and reimbursement strategy across the Immunology therapeutic area. This role shapes enterprise-level...

The Executive Director, Network Strategy Execution (NS&E) and Product Source Management is responsible for setting the strategic direction and leading execution of global product source changes and network rationalization activities, where applicable. This role ensures delivery of business priorities, execution excellence, and alignment across a complex, global manufacturing network. The Executive Director operates in a managerial capacity, overseeing a team of Directors and their respective teams to manage a portfolio of strategic sourcing change and network execution initiatives. This role partners closely with Manufacturing Operating Unit leaders, site leadership, and cross-functional stakeholders across Operations, Supply Chain, Quality, Regulatory, Technical, Finance,...

Our US Ophthalmology team is dedicated to improving the lives of patients with diabetic macular edema (DME) and neovascular age-related macular degeneration (nAMD) through a pipeline of two investigational therapies. We pursue this mission through patient focus, innovation, expanded access to transformative treatments, and collaboration with healthcare systems, governments, and payers. Grounded in scientific rigor and flawless execution, we aim to bring breakthrough therapies to the patients who need them most. The Executive Director, US Marketing Leader will lead U.S. marketing strategy and execution for the first launch, a late-stage pipeline asset for DME and nAMD, while also shaping early...

POCS – Rahway Senior Technician, Operations (FLEx Non-Sterile Technician) Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement The candidate will be working with process engineers and formulations in oral solid and liquid dosage forms. The position requires someone who can demonstrate good attention to detail and achieve a consistent error-free execution of daily job responsibilities, be able to complete documentation using Good Documentation Practices and be able to identify opportunities for process improvement and employ basic problem-solving skills ....

Phlebotomist About the role Every day, the donors you meet will motivate you. The high-quality plasma you collect will become life-changing medicines. Here, a commitment to customer service and quality is expected. You will report to the Plasma Center Manager and will perform as a plasma donor screener and perform phlebotomy to support plasma center operations. How you will contribute · You will greet donors as they enter and exit the donor floor. · You will perform venipuncture of donors and programming of plasmapheresis machine. · You will monitor donors during the donation process and manage donor reactions. · You...

About BioLife Plasma Services Every day, the donors you meet will motivate you. The high-quality plasma you collect will become life-changing medicines. Here, a commitment to customer service and quality is expected. You will report to the Plasma Center Manager and will perform as a Medical Support Specialist (Plasma Center Nurse) to support plasma center operations. BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. About the role Every day, the donors you meet will motivate you. The high-quality plasma you collect will become life-changing medicines. Here, a commitment to customer service and quality is expected. You will...

Specialty Representative/Senior Specialty Representative Live What you will do In this vital role you will be the connection to our customers by providing clinical knowledge of our products to medical professionals and helping them navigate the complex payer environment. We are actively searching for a Specialty Representative or Senior Specialty Representative to deliver on our commitment to serve patients. The Specialty Representative/Senior Specialty Representative acts as the primary customer contact and is responsible for implementing marketing strategy and promoting Amgen products as led by the District Manager. Amgen supports and encourages our team members to have long term, fulfilling...

Sr Director, Global Regulatory Strategy, Neuroscience Will be a key member of the GRSP Extended Leadership Team to ensure the development, implementation, and alignment of regulatory strategies across projects and the Neuroscience therapeutic area. Acts as regulatory representative on various company-wide projects and initiatives. Support due diligence and business development assessments. Working with regional regulatory staff as Global Regulatory Lead and US Regional Regulatory Lead on assigned development assets and marketed products Develop global therapeutic regulatory strategies and operational plans for identified investigational and marketed products. Review/provide counsel on product development plans. Assemble the global regulatory plans for identified projects/products....

This position will support the Surgical Sutures’ Manufacturing business within Medtronic’s Surgical Innovations group located in North Haven, CT. We are seeking a Senior Quality Engineer to join our team in North Haven, CT. This role is integral to ensuring the highest standards of quality and compliance in our medical device manufacturing processes. As a key member of our Quality team, you will collaborate cross-functionally to enhance product reliability, optimize processes, and uphold regulatory compliance. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our...

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together. ...

Business Introduction GSK sigue comprometida a alcanzar ambiciosos objetivos comerciales para el futuro. Para 2031, nuestro objetivo es generar £40 mil millones en ventas anuales, aprovechando nuestro sólido impulso de desempeño existente para aumentar significativamente nuestro impacto positivo en la salud de miles de millones de pacientes en todo el mundo. Nuestra estrategia Ahead Together se centra en la intervención temprana para prevenir y alterar el curso de las enfermedades, protegiendo así a las personas y apoyando a los sistemas de salud. Nuestro diverso portafolio abarca vacunas, medicamentos especializados y medicamentos generales. A través de la innovación continua y un...

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe. Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our head office and BlueSky Hub in downtown Toronto are purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm...

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality! If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person. We are hiring a Global Clinical Head (GCH) for Obesity/Diabetes in our Late Cardiovascular, Renal and Metabolism (CVRM) Global Development team. This is a key role where you, with your strong leadership skills and drug development experience, will impact and drive development programs in a...

The rotations are carried out in a variety of work environments such as corporate and division headquarters, manufacturing plants and other operating environments. A senior financial leader is assigned to each FPDP to mentor and advise you while on the program. Assignments are located in multiple areas of the world US Lake County, IL Columbus, OH Austin, TX Twin Cities, MN Multiple cities in California Europe Germany UK Netherlands Ireland Switzerland Belguim Asia Singapore Latin America Brazil Costa Rica Colombia Basic Qualifications Completion of a bachelor’s degree in Finance, Accounting, Economics, Business or similar Geographically mobile and willing to...

Help us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Positionsübersicht Der/Die Facilities Coordinator III arbeitet eng mit dem Managementteam der Abteilung Facility Management zusammen, um verschiedene Facility-Aktivitäten zu unterstützen und die Rollen, Aktivitäten und Prozesse der Facility Coordinators über mehrere Standorte hinweg zu harmonisieren. Diese Position bietet administrative Unterstützung...

Our Team The candidate will be part of a dynamic interactive Preclinical Safety group that spans all aspects of the drug development value chain providing toxicology and safety pharmacology expertise as a member of global project teams. Given the activities performed by the group, internal (within Preclinical Safety and with other project functions) and external (collaboration partners) interactions occur on a daily basis making for a diverse work environment. You will Be exposed to all aspects of the drug development chain Have diverse opportunities to provide toxicology scientific input and apply those expertise Be recognized by Management and Project Teams...

Join the team protecting half a billion lives every year with next-gen science, mRNA innovation, and AI-driven breakthroughs. In Vaccines, you’ll help advance prevention on a global scale - and shape the future of immunization. The Head of Vaccine Global Project Management leads New Vaccines R&D project management function, translating corporate strategy into executable project plans while ensuring strategic alignment, operational excellence, and delivery of complex vaccine development programs. You will be responsible for establishing best-in-class project management standards, governance frameworks, and AI/Digital-enabled practices across the portfolio — with the ultimate goal of delivering vaccines at optimal time-to-market, within budget,...

The Genomic Medicine Unit (GMU) CMC group at Sanofi is dedicated to the establishment of best-in-class manufacturing platforms to support development of life-changing advanced cell and gene therapy products, including recombinant AAV vectors, lentiviral vectors and cell therapy products. Sanofi is looking for an experienced cell culture development professional with experience in cell therapy process development to join the Genomic Medicine Cell Therapy Process Development Group located in Waltham, MA in the role of Senior Scientist. The Genomic Medicine Cell Therapy Development group within Sanofi operates with the mission to develop robust, scalable, and innovative cell culture processes for Sanofi’s...

Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you’ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs. Job Summary The Medical Evidence and Outcomes Research Lead will serve as a Center of Excellence for managing local evidence generation partnerships across the North America Specialty Care portfolio. Working closely with key stakeholders across Global and US medical units, clinical development, RWE, HEVA, Access Strategy, and commercial functions, this role will identify and prioritize local evidence needs, ensure strategic alignment between local and...

Johnson & Johnson (J&J) is recruiting for a Sr Manager, Project Controls (PC), Cost Lead , located in Wilson, NC to support Bio, NC. About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at At Engineering & Property Services (E&PS) we take care of all J&J buildings around the...

About Orthopaedics Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery. Your unique talents will help patients on their...

About Surgery Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer. Patients are waiting. Your unique talents will help patients on their journey to...

The Senior Manager Regulatory Affairs US Advertising and Promotion-Immunology combines knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet the required legislation. Additionally, the individual develops and supervises regulatory professionals as needed. Supports the Director in efforts to influence the regulatory environment. The Senior Manager has department/group/site level influence and is generally recognized as an expert and resource and leads the department as a subject matter expert (SME) for Regulatory. This individual share knowledge and expertise with others in support of team activities and analyzes broad scope implications of changing regulations...

Purpose The Meeting Account Manager manages and supports all operational and logistical activities for meeting and event related activities, may liase with a third party vendor as appropriate. The Meeting Account Manager is responsible for working closely with specified clients to follow a comprehensive meetings and events calendar that aligns with business owner strategies and objectives. This role works closely with internal counterparts to execute successful meetings and events. Responsibilities Implementation and maintenance of the effectiveness of the quality system by ensuring strategic meeting management operations and standards for their customer account base. Consult with the internal stakeholders in the...

The Senior Manager Regulatory Affairs US Advertising and Promotion-Immunology combines knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet the required legislation. Additionally, the individual develops and supervises regulatory professionals as needed. Supports the Director in efforts to influence the regulatory environment. The Senior Manager has department/group/site level influence and is generally recognized as an expert and resource and leads the department as a subject matter expert (SME) for Regulatory. This individual share knowledge and expertise with others in support of team activities and analyzes broad scope implications of changing regulations...

The Senior Manager Regulatory Affairs US Advertising and Promotion-Immunology combines knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet the required legislation. Additionally, the individual develops and supervises regulatory professionals as needed. Supports the Director in efforts to influence the regulatory environment. The Senior Manager has department/group/site level influence and is generally recognized as an expert and resource and leads the department as a subject matter expert (SME) for Regulatory. This individual share knowledge and expertise with others in support of team activities and analyzes broad scope implications of changing regulations...

This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience. Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations. Responsibilities Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those...

The Senior Manager Regulatory Affairs US Advertising and Promotion-Immunology combines knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet the required legislation. Additionally, the individual develops and supervises regulatory professionals as needed. Supports the Director in efforts to influence the regulatory environment. The Senior Manager has department/group/site level influence and is generally recognized as an expert and resource and leads the department as a subject matter expert (SME) for Regulatory. This individual share knowledge and expertise with others in support of team activities and analyzes broad scope implications of changing regulations...

The Clinical Document Management Associate II will ensure the Master File is always inspection-ready and complies with ICH GCP guidelines. This role entails the conduct of rigorous quality checks, ensuring reliable and complete Trial Master File. Collaborate with study teams, providing support to address and resolve issues related to Master File health indicators. Focus on maintaining the completeness, accuracy, and timeliness of all crucial documents throughout the lifecycle of the assigned clinical trials. This job is located onsite in our North Chicago office. We can also considering hiring out of our Irvine, CA office. Responsibilities Actively engages with document owners...

The Senior Manager Regulatory Affairs US Advertising and Promotion-Immunology combines knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet the required legislation. Additionally, the individual develops and supervises regulatory professionals as needed. Supports the Director in efforts to influence the regulatory environment. The Senior Manager has department/group/site level influence and is generally recognized as an expert and resource and leads the department as a subject matter expert (SME) for Regulatory. This individual share knowledge and expertise with others in support of team activities and analyzes broad scope implications of changing regulations...

Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. As trailblazer in anti-FcRn technology, the Company is developing innovative, targeted therapies to meet the complex and variable needs of people with autoimmune diseases. Immunovant is seeking a detail-oriented and experienced Senior Manager, R&D Accounting to join our accounting team. This role you will assist with the clinical trials and R&D accruals processes and work closely with Clinical Operations, Manufacturing, and R&D teams. You will apply your existing accounting skills and knowledge, learn new skills, and play a key role in guiding...

The Director, AI Architecture & Governance is a senior technical leadership role responsible for defining and governing enterprise-scale AI and Generative AI architectures across the life sciences value chain. This role establishes the standards, platform/tooling strategy, and governance frameworks required to deliver AI outcomes safely and at scale, while enabling AI/ML engineering resources to execute efficiently. The Director partners closely with Enterprise Systems, Computer System Validation (CSV), and Enterprise Data Systems (EDS) to ensure AI solutions align with application architecture, validation expectations, and enterprise data governance. Success requires strong cross-functional collaboration and communication across scientists, engineers, data teams, and executive...

Sarepta Therapeutics is seeking a highly motivated and experienced Senior AI/ML Engineer to join our technology teams. This is a unique opportunity to be a foundational member of a new innovative team that will drive adoption of artificial intelligence and machine learning across the organization. The successful candidate will deliver prioritized AI/ML use cases—initially focused on R&D workflows and expanding into clinical and regulatory use cases as capabilities mature—while operating within enterprise architecture, governance, and data standards. This role requires deep technical expertise, strong problem framing, and the ability to collaborate and communicate effectively with cross-functional teams. The Opportunity to...

ROLE SUMMARY As part of the Clinical Data Sciences (CDS) group, an integral delivery unit within the Clinical Development & Operations (CD&O) organization, the Associate Data Manager is responsible for timely and high quality data review and query management of clinical data supporting the Pfizer portfolio. The Associate Data Manager executes on key data management deliverables used to collect, review, monitor, and ensure the integrity of clinical data. ROLE RESPONSIBILITIES Participate in CDS activities including data review and query management, assist with quality database design including documentation, testing, validation, and implementation of clinical data collection tools, CRF and non-CRF, using...

ROLE SUMMARY This position performs business operations planning and management for Vaccines Research and Development activities, to ensure timely and compliant conduct of vaccine development programs. The incumbent applies a comprehensive understanding of the pharmaceutical and vaccine research and development processes as well as budget planning expertise to independently guide cross-functional vaccine development program teams, formulating and delivering resource and funding plans required to secure program funding. The incumbent provides input and influence to both program development and internal governance strategy and will independently provide consultation to vaccines leadership on resource deployment issues. Collaborates with, and serves as an advisor...

About MedTech Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at Johnson & Johnson MedTech Surgery is currently recruiting for a Digital & Systems Lead WCH Ethicon, part of the Johnson & Johnson MedTech Surgery business, is the worldwide leader in wound closure devices with products that help improve patient outcomes, optimize healing, and maximize operating room efficiency. Johnson & Johnson has made significant contributions to surgery for more than 60 years from...

About MedTech Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at Johnson & Johnson MedTech Surgery is currently recruiting for a Senior Technology Engineering Manager to join the Technology, Strategy, & Innovation team within Wound Closure & Healing Global Technical Operations! Ethicon, part of the Johnson & Johnson MedTech Surgery business, is the worldwide leader in wound closure devices with products that help improve patient outcomes, optimize healing, and maximize operating room efficiency....

We are searching for the best talent for Sales Associate to be in Minneapolis, MN territory. About Orthopaedics Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot...

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s) Cork, Ireland & Diegem, Belgium - Requisition Number R-078179 Zug/Zuchwil, Switzerland - Requisition Number R-079116 Raritan/Titusville/Bridgewater/Raynham- - Requisition Number R-083003 DePuy Synthes, a market-leading Medical Devices business within Johnson & Johnson, has an outstanding opportunity for a Lead Financial Analyst within the project space. Seeking an enthusiastic self-driven individual who will...

Johnson & Johnson Innovative Medicines is recruiting for a Medical Science Liaison – GU Oncology to be based in the N. IL | WI territory. Therapeutic Area GU Oncology The Medical Science Liaison (MSL) is considered the field based scientific and clinical emerging expert on current and future Johnson & Johnson Innovative products. The MSL is responsible for developing and enhancing professional relationships with Key thought leaders/HCPs and providing fair balanced, objective, non-promotional scientific information, and education to health care professionals. The MSL drives high quality scientific exchange, territory execution, and actionable insight generation while maintaining‑ the highest standards of...

DePuy Synthes is recruiting for a Director, Operations Leadership & Learning, this hybrid position will be located in Rayhnam, MA (USA). Alternate Hybrid locations maybe considered at Raritan, NJ (USA); West Chester, PA (USA); Palm Beach Gardens, FL (USA); Raynham, MA (USA); Warsaw, IN (USA); Zuchwil, Switzerland or Loughbeg, Ringaskiddy Ireland. Johnson & Johnson announced plans to separate our Orthopedics business to establish a standalone orthopedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months , subject to legal requirements, including consultation with works councils and other employee...

DePuy Synthes is recruiting for a Director of Acquisitions & Divestitures , this hybrid position will be located in Rayhnam, MA (USA). Alternate Hybrid locations maybe considered at Raritan, NJ (USA); West Chester, PA (USA); Palm Beach Gardens, FL (USA); Raynham, MA (USA); Warsaw, IN (USA); Zuchwil, Switzerland or Loughbeg, Ringaskiddy Ireland. Johnson & Johnson announced plans to separate our Orthopedics business to establish a standalone orthopedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months , subject to legal requirements, including consultation with works councils and other...

Johnson & Johnson Vision, Inc. is currently hiring a Materials Engineer, to join its dynamic team located in Anasco, PR. The Engineer is directly responsible for leading multiple raw material and molding related projects for the manufacture of inter-ocular lenses (IOL) at our site. They will lead multi-functional project teams and ensure that projects are completed on time and within budget. The Engineer will be an integral member of the Materials Engineering team in Anasco, PR and be fully accountable for Business Continuity, Validations, Cost Improvement and Supplier Enabled Innovation/Process Changes. The candidate should be able to possess an ability...

At BioLife, we know that flexibility matters—especially for those balancing multiple commitments. That's why we're dedicated to creating meaningful part-time opportunities for our team. This role is truly part-time , with most shifts lasting between 4 to 6 hours a day, 3+ days per week —designed to fit your life. We’ll confirm your availability and shift days and times early in the interview process. And, because we value open communication, you’ll always be informed about any schedule changes in advance. Our patients depend on the plasma we collect, so your reliability during your scheduled hours is greatly valued....

*Please note this is a plasma donor assessment and monitoring role. About BioLife Plasma Services Every day, the donors you meet will motivate you. The high-quality plasma you collect will become life-changing medicines. Here, a commitment to customer service and quality is expected. You will report to the Plasma Center Manager and will perform as a Medical Support Specialist (Plasma Center Nurse) to support plasma center operations. BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. About the role Every day, the donors you meet will motivate you. The high-quality plasma you collect will become life-changing medicines. Here,...

About BioLife Plasma Services Every day, the donors you meet will motivate you. The high-quality plasma you collect will become life-changing medicines. Here, a commitment to customer service and quality is expected. You will report to the Plasma Center Manager and will perform as a Medical Support Specialist (Plasma Center Nurse) to support plasma center operations. BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. About the role Every day, the donors you meet will motivate you. The high-quality plasma you collect will become life-changing medicines. Here, a commitment to customer service and quality is expected. You will...

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Senior Director, Head of Oncology Alliance Management in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering...

We're building a connected, end-to-end Enterprise AI engine - uniting data foundations, AI technology, process reinvention, and business-facing AI to accelerate results across the whole value chain. Success depends on being exceptional connectors you'll actively leverage existing capabilities, celebrate and promote reuse, export breakthrough ideas across geographies and functions, and obsess over scaling impact rather than building in isolation. If you thrive in high-collaboration environments where your role is to turn complex, cross-functional problems into reusable, enterprise-wide capabilities - and where the measure of success is adoption and scale, not just innovation - you'll have the platform (and sponsorship)...

Senior Medical Representative - R&I Location Eastern Alkhobar ABOUT ASTRAZENECA AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. SITE DESCRIPTION AstraZeneca is experiencing a significant transformation in the Kingdom of Saudi Arabia, driven by a commitment to advancing healthcare, innovation, and sustainable growth. Building on our global legacy, AZ KSA is rapidly evolving its operations to better serve patients, collaborate with healthcare stakeholders, and contribute to the ambitious goals outlined...

Senior Medical Representative – R&I Location Eastern Alkhobar ABOUT ASTRAZENECA AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. Join a high-performing team, empowered to cut through the noise and drive real change. Our agility and pace, coupled with scientific focus, powers us to spot opportunities in the market that keep us moving forward and into new spaces. SITE DESCRIPTION AstraZeneca is experiencing a significant transformation in the Kingdom of Saudi...

We are seeking a highly motivated and creative scientist to join the Functional Genomics cluster within the Target, Disease, and Systems Biology function in Sanofi Research. They will drive the application of functional genomics target ID and validation to advanced disease models in order to elucidate disease mechanisms and discover novel targets across immunology, ophthalmology, neurology, oncology, and rare disease. The successful candidate will collaborate closely with therapeutic area colleagues to advance functional genomics target discovery and validation and develop new screening workflows in advanced disease models including primary cells, iPSC-derived cells, and co-culture/organoid systems. This is a unique opportunity...

We are seeking a highly motivated Senior Principal Scientist to spearhead the execution and expansion of our mast cell disorders Research & Development pipeline. A successful candidate will have deep expertise in hematopoietic stem cell biology with a particular focus on mast cell disorders and related immune disorders in the context of rare diseases. This individual will work cross-functionally to identify and shepherd early-stage programs into the research pipeline, through internal and external innovation, and ensure the successful progression of development stage programs through the clinic to registration by providing deep research subject matter expertise. In parallel, the candidate will...

Overview The Marketing Operations, Senior Manager works cross-functionally to project manage the review process for advertising and promotional materials for approved drug and/or device products. In addition, the Senior Manager is responsible for identifying and leading specific Marketing Operations individuals, function(s) and/or special projects, required to achieve the designated brand(s) objectives. The Senior Manager act as a Marketing Operations subject matter expert for the PRC (promotional Review Committee) review process and is responsible for ensuring the process efficiency involving Medical, Legal, Regulatory, and Compliance teams, while conforming with company policies and procedures. RESPONSIBILITIES People/team mentoring and coaching. Recruit, coach and...

AbbVie’s Global Internal Audit function plays a critical role in protecting and enhancing the organization’s value through risk-based assurance and advisory services to internal stakeholders, senior management, and our Audit Committee of the Board. Internal Audit strives to be a critical function to evaluate company, industry and emerging risks, effectively partnering with the business, and consistently recruit and develop key talent. Our goals are carried-out through the talent of the audit team, while leveraging analytical and audit tools, supported by a dynamic and collaborative team culture. Responsibilities Internal Audit Key Pillar Execution Our leading pillar is focused on executing our...

Allergan plc (NYSE AGN) is a bold, global pharmaceutical company and a leader in a new industry model - Growth Pharma. Allergan is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for patients around the world. Allergan markets a portfolio of leading brands and best-in-class products for the central nervous system, eye care, medical aesthetics and dermatology, gastroenterology, women's health, urology and anti-infective therapeutic categories. With commercial operations in approximately 100 countries, Allergan is committed to working with physicians, healthcare providers and patients to deliver innovative and meaningful treatments that help people around...

Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations. Responsibilities Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. in order to meet or exceed on those objectives. Create pre-call plan using SMART objectives and execute post-call evaluation in order to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and...

This a MD/MA Pack, A1 Day Shift 7am-730pm Sunday/Monday/Tuesday & every other Wednesday The Production Specialist I will work in a high performing and fast-paced pharmaceutical finishing operation in order to meet our production requirements while maintaining the utmost focus on safety and quality. He or she will support setup, changeover and packaging of pharmaceutical products. He or she will be expected to contribute to and build a team environment by working together with his or her peers daily on a finishing line. He or she will be responsible for creating a quality-focused environment by motivating/influencing others and always driving...

Leads the direction, planning, execution, and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in and may lead cross-functional teams to generate, deliver, and disseminate high-quality clinical data supporting overall product scientific and business strategy. Responsibilities Leads and demonstrates ownership of the design and implementation of multiple clinical development programs (or one large, complex program) in support of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations, and emerging issues. Oversees project-related education of investigators, study site personnel, and...

The Director, Health Economics & Outcomes Research (HEOR) leads the strategic development & execution of high-quality evidence for an enterprise-critical gene therapy in retina diseases. He or she directly contributes to the launch evidence required for JCA and HTA, and serves as the brand/asset leader representing HEOR on cross functional asset/brand teams, ensuring HTA/payer evidence requirements are reflected in the overall asset strategy. He or she may be accountable for more than one asset and/or indication, and oversees evidence alignment across key international markets. Responsibilities Oversees the design and conduct, of projects and effectively communicates the findings and strategic impact...

This a MD/MA Pack, A1 Day Shift 7am-730pm Sunday/Monday/Tuesday & every other Wednesday The Production Specialist I will work in a high performing and fast-paced pharmaceutical finishing operation in order to meet our production requirements while maintaining the utmost focus on safety and quality. He or she will support setup, changeover and packaging of pharmaceutical products. He or she will be expected to contribute to and build a team environment by working together with his or her peers daily on a finishing line. He or she will be responsible for creating a quality-focused environment by motivating/influencing others and always driving...

Lead strategic and tactical elements of the brand strategy and tactical plan for IMBRUVICA in CLL, including value propositions, positioning, segmentation, and creative development. Develop and articulate effective oncology marketing strategies that are impactful, executable, easily communicated, and clinically/financially supported for relevant areas of responsibility (product/indication/channel). Internally, the Associate Director will foster positive working relationships with the sales force, medical affairs, market research, sales training, regulatory, and other cross-functional marketing teams. Externally, they will work with various agencies, consultants, physicians, and other marketing partners to successfully drive the business. The candidate must be able to operate in a fast-paced organization,...

Thank you for considering a future opportunity with our company! We are not currently hiring for this specific role, but we would love to connect with talented individuals who are interested in potential future positions. By joining our talent pipeline, you will be the first to be notified when suitable opportunities arise. In this talent pipeline requisition, we are not actively recruiting for this position at the moment. However, we are building a network of exceptional individuals who possess the skills and experience required for future openings. By submitting your application to this requisition, you will be added to our...

Purpose Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance. Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials. Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience. Responsibilities Considered as the primary point of contact for the investigative site. High level of competency or experience in providing contextual information on the clinical trials, connects...

This a MD/MA Pack, A2 Night Shift 7pm-730am Sunday/Monday/Tuesday & every other Saturday (15% pay increase for nights) The Production Specialist I will work in a high performing and fast-paced pharmaceutical finishing operation in order to meet our production requirements while maintaining the utmost focus on safety and quality. He or she will support setup, changeover and packaging of pharmaceutical products. He or she will be expected to contribute to and build a team environment by working together with his or her peers daily on a finishing line. He or she will be responsible for creating a quality-focused environment by...

About the Team The Targeted Lipid Nanoparticle (tLNP) drug product development group within AbbVie’s tLNP CMC team is committed to advancing clinical-stage tLNP assets from First-in-Human (FIH) through Phase 2. The team collaborates across biologics discovery, CMC partners, Clinical Operations, Regulatory Affairs, Quality Assurance, and external manufacturing to support development and commercialization of tLNP products. Key focus areas include establishing robust formulation and process development capabilities, leading critical CMC activities for pipeline programs, devising formulation development strategies, conducting stability evaluations, optimizing clinical in-use strategies, developing innovative product presentations, implementing stage-based quality risk management, and driving scientific initiatives to ensure the...

The primary job function of this position is to provide technical support to cross-functional teams working with little or no supervision, apply project management knowledge, engineering and product/process knowledge, and ingenuity to complete medium size projects from concept through project closure within or across disciplines. Responsibilities Support and monitor Production as required to troubleshoot material, process and equipment problems including product loss and inefficiencies. Utilize technical abilities and experience, including the use of structured analytical techniques and technical tools such as data acquisition (manual and computerized), data analysis – especially including process capability analysis, SPC and other statistical tools. Provide...

“Master File Owner” responsible for managing and ensuring inspection readiness of clinical documentation / master files. CDC representative on study team(s) with ownership of the study Trial Master File (TMF). Contributes to functional area development by being a subject matter expert for CDC and TMF stakeholders. Responsibilities Ensures real-time inspection readiness of clinical documentation / TMF by performing quality control (QC) of the TMF/artifacts to ensure completeness, document quality and timeliness of upload of artifacts to the TMF. Collaborate with Artifact owners; holds study team members accountable for respective sections of the TMF, reports status to study team members by...

For the Senior Scientist I position, we are seeking a highly motivated candidate who can conceive, implement and execute novel scientific research and development, independently develop, optimize new methods and techniques to generate reliable and reproducible data in a timely manner and demonstrate broad versatile technical expertise. They will support early phase development of New Chemical Entities (NCEs), particularly synthetic peptides, in both the preclinical- and clinical-development space and collaborate within the global Analytical R&D organization and with R&D cross-functional partners such as Pre-Clinical Safety (PCS), Process Chemistry, Process Engineering, Drug Product Development (DPD), Quality Assurance (QA), and CMC-Regulatory Affairs....

The Knowledge Management and Strategic Initiatives role will develop & advocate strategic positions for CMC regulatory/CMC issues with cross functional internal stakeholders and on behalf of AbbVie in key areas that will meaningfully impact acceleration of AbbVie’s portfolio. This can be accomplished through active engagement with internal cross-functional and external groups and serving as a scientific/technical resource within RA CMC that provides guidance/direction to our staff to develop robust product strategies that integrate CMC regulatory policy and expectations. Responsibilities Deliver strategic CMC regulatory insights and guidance to cross functional stakeholders by sharing expertise, monitoring industry trends, and implementing emerging regulatory...

The Supervisor, Security Systems will be responsible for enterprise-wide security systems including access control, surveillance, intrusion detection and other programs required for the protection of AbbVie resources and assets. This role will provide strategic guidance and tactical support for new installations, upgrades to existing systems and problem resolution for AbbVie sites globally. This position requires strong collaboration and influence with other AbbVie functions and outside service providers. Responsibilities Accountable for planning, development, and deployment of security systems for AbbVie locations globally. This role develops (no coding) physical security plans (access control, surveillance and alarms) for our sites and configures the...

With supervision, oversees the direction, planning, execution and interpretation of clinical trials or research activities of a clinical development program. Participates in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy. Responsibilities With appropriate supervision, manages the design and implementation of study protocols for a clinical development program in support of the overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations, and emerging issues. Oversees project-related education of investigators, study site personnel, and AbbVie study staff. Has responsibility for...

This a MD/MA Pack, A2 Night Shift 7pm-730am Sunday/Monday/Tuesday & every other Saturday (15% pay increase for nights) The Production Specialist I will work in a high performing and fast-paced pharmaceutical finishing operation in order to meet our production requirements while maintaining the utmost focus on safety and quality. He or she will support setup, changeover and packaging of pharmaceutical products. He or she will be expected to contribute to and build a team environment by working together with his or her peers daily on a finishing line. He or she will be responsible for creating a quality-focused environment by...

The Global Supply Planner (GSP) is responsible for the short-term or end-to-end (E2E) range supply chain planning activities and controlling the flow of product globally between manufacturing sites and the distribution centers. The objective is to meet market demand and optimize inventory levels in our supply network. To achieve this, the GSP must build strong relationships with supply sites, brand operation managers, ECM managers, Quality Assurance, Finance, Distribution, the Affiliates, and other stakeholders. The GSP knows the business and can anticipate future opportunities and risks, and continuously looks to raise the bar to ensure success for AbbVie and assurance of...

Talent will be hired at a level commensurate with experience. This role is field-based, and candidates should live within a reasonable distance from the primary city. The geography includes the following areas Grand Rapids, MI Fort Wayne, IN Toledo, OH Immunology Account executives serve as a resource for hospitals, group practices and specialty pharmacies that are focused on treating immunological diseases including rheumatoid arthritis, psoriatic disease, atopic dermatitis, and Crohn’s disease. Responsibilities include learning and development of key account management skills including immunology franchise collaboration and communication, non- branded value based acumen, effective business planning, targeted account execution to deliver...

Purpose Process Engineers in Product Development Science & Technology support API projects through all the phases of late stage development, commercialization, product life cycle. This position will be responsible to ensure processes can be run safely, addressing scale-up issues and developing and implementing robust API process steps from the lab to a manufacturing environment. Once commercialized, the Process Engineer is responsible for continuous improvement activities, technical transfer to manufacturing sites, and resolution of technical manufacturing issues in a commercial setting. Effective cross functional interactions with quality and regulatory functions and on-site manufacturing personnel is key for successful job performance. The...

Overview The Marketing Operations, Senior Manager works cross-functionally to project manage the review process for advertising and promotional materials for approved drug and/or device products. In addition, the Senior Manager is responsible for identifying and leading specific Marketing Operations individuals, function(s) and/or special projects, required to achieve the designated brand(s) objectives. The Senior Manager act as a Marketing Operations subject matter expert for the PRC (promotional Review Committee) review process and is responsible for ensuring the process efficiency involving Medical, Legal, Regulatory, and Compliance teams, while conforming with company policies and procedures. RESPONSIBILITIES People/team mentoring and coaching. Recruit, coach and...

Overview The Marketing Operations, Senior Manager works cross-functionally to project manage the review process for advertising and promotional materials for approved drug and/or device products. In addition, the Senior Manager is responsible for identifying and leading specific Marketing Operations individuals, function(s) and/or special projects, required to achieve the designated brand(s) objectives. The Senior Manager act as a Marketing Operations subject matter expert for the PRC (promotional Review Committee) review process and is responsible for ensuring the process efficiency involving Medical, Legal, Regulatory, and Compliance teams, while conforming with company policies and procedures. RESPONSIBILITIES People/team mentoring and coaching. Recruit, coach and...

This is a hybrid role including in office and remote working days. Must be a resident or relocatable to Austin TX area. Must be able to work one of the below shifts 800am-430pm CT, or 830-500pmCT, 730-430pmCT or 800-5pmCT The Sr Inside Sales Business Development Manager is a revenue generating position with responsibility for quarterly sales quota attainment for the Facial Aesthetics portfolio of products (BOTOX® Cosmetic, JUVÉDERM® Collection of Fillers, SkinMedica®, KYBELLA®) and for managing and enhancing portfolio growth through business development activities using primarily phone communication. The Sr IBDM represents the Allergan Aesthetics product portfolio to targeted aesthetic...

As a Customer Service Supervisor, your primary responsibilities will include providing guidance and support to your team members, training and developing their skills, monitoring performance, managing workloads, facilitating communication and coordination, solving problems and escalating issues as needed, conducting performance evaluations, and fostering a collaborative team environment. You will play a critical role in ensuring effective customer service delivery, optimizing team performance, and promoting continuous growth and development among the team members. If you are interested in joining our team that strives for excellence and growth opportunities, we encourage you to submit your resume. Let's discuss how your expertise can...

Performs a variety of routine sample preparation and analysis procedures to support Manufacturing and Quality Operations. Follows validated or experimental analytical procedures with periodic direct supervision. Revision and compilation of results and data comparison against test method acceptance criteria, methodology, protocol and product specifications. Responsibilities Perform method troubleshooting. Perform laboratory and/or manufacturing investigations and studies. Write technical documentation according to established procedures. Perform tasks related to commercial and non-commercial production, technology transfer and/or validation projects. Maintain statistical control charts for the department’s Laboratory or process monitoring. Responsible to comply with AbbVie and Quality Operations policies, plant procedures, and GMP and...

Talent will be hired at a level commensurate with experience. This role is field-based, and candidates should live within a reasonable distance from the primary city. The geography includes the following areas Grand Rapids, MI Fort Wayne, IN Toledo, OH Immunology Account executives serve as a resource for hospitals, group practices and specialty pharmacies that are focused on treating immunological diseases including rheumatoid arthritis, psoriatic disease, atopic dermatitis, and Crohn’s disease. Responsibilities include learning and development of key account management skills including immunology franchise collaboration and communication, non- branded value based acumen, effective business planning, targeted account execution to deliver...

Leads the direction, planning, execution, and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in and may lead cross-functional teams to generate, deliver, and disseminate high-quality clinical data supporting overall product scientific and business strategy. Responsibilities Leads and demonstrates ownership of the design and implementation of multiple clinical development programs (or one large, complex program) in support of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations, and emerging issues. Oversees project-related education of investigators, study site personnel, and...

Purpose Primarily responsible for ensuring adherence to GLP regulations and developing an organizational model for the Quality Assurance Unit. Manage a team of audit professionals responsible for quality oversight of all GLP-regulated studies. Poor decisions could present significant risks to patients in clinical trial programs, jeopardize the outcome of pre-clinical or clinical trials with resulting adverse business impact, or result in rejection of regulatory filings owing to compliance issues. These outcomes would adversely affect sales, margin, and stockholder value. Responsibilities Manage auditing for compliance of all GLP-regulated in-house studies and regulatory dossiers prior to filing. Collaborate with GXP...

Body Contouring- CoolSculpting The Regional Practice Manager has general responsibilities for overseeing the Practice Development Managers in the assigned region and supporting their efforts to develop customer relationships and drive utilization in each assigned territory. This individual will have high accountability for achieving the regional consumable sales quotas and objectives. Essential Duties and Responsibilities include the following (other duties may be assigned.) Achieving sales and utilization quota results in the assigned region. Responsible for ensuring the Practice Development team is performing effective territory penetration, coverage and account identification to drive sales and increase the utilization of the Company’s consumable products....

The Principal Data Scientist will serve as a strategic leader and technical expert driving enterprise-level transformation through the convergence of R&D data assets and the systematic integration of advanced AI/ML capabilities into organizational workflows. This role will work with cross-functional teams to define and architect scalable solutions that fundamentally transform how AbbVie leverages data and artificial intelligence to enhance strategic decision-making processes across the R&D pipeline and clinical development continuum. Acting as a key member of the R&D Convergence Core team, this position will identify systemic gaps in data convergence and workflow integration, then lead collaborative efforts to design...

The Associate Data Engineer II will build, maintain, and optimize data infrastructure - like databases and data pipelines - that address cross-functional critical business needs. This role is expected to improve existing methods and processes by using various languages to pull and manipulate data, develop and maintain ETL pipelines, implement quality control and monitoring processes to maintain accurate data flows, maintain comprehensive documentation of process designs, test results, and pipeline configurations, etc. This hire is expected to demonstrate proficiency in information technology engineering, including data warehousing. Responsibilities Independently design and develop data solutions to address business challenges. Demonstrate proficiency across...

The Senior Specialist, Communications , leads the development and execution of executive-sponsored communications and culture initiatives for the Commercial Business Technology Solutions organization as well as the development and execution of Executive-sponsored communications and culture initiatives. In partnership with the Commercial BTS Vice President and senior leadership team, this role drives strategic messaging and campaigns, representing the executive's voice, while reinforcing a consistent, unified BTS across BTS Commercial, strengthening alignment with the BTS Performance Roadmap and priorities. This includes leadership communications, employee engagement programs, town halls, newsletters, branding initiatives, and digital platforms like Teams and SharePoint. Key responsibilities include producing...

This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience. Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations. Responsibilities Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those...

Allergan plc (NYSE AGN) is a bold, global pharmaceutical company and a leader in a new industry model - Growth Pharma. Allergan is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for patients around the world. Allergan markets a portfolio of leading brands and best-in-class products for the central nervous system, eye care, medical aesthetics and dermatology, gastroenterology, women's health, urology and anti-infective therapeutic categories. With commercial operations in approximately 100 countries, Allergan is committed to working with physicians, healthcare providers and patients to deliver innovative and meaningful treatments that help people around...

We're seeking a technically-savvy Business Analyst to bridge the gap between our Customer Operations project specialists and Business Technology development teams. You'll be the 'technical translator' who speaks both business and developer language fluently, reducing clarification cycles and accelerating our call center system enhancements. As our team's technical capabilities mature, this role will evolve from requirements translation into strategic analysis—evaluating implementation processes, analyzing system performance (e.g. Salesforce case management, chat/SMS adoption), and assessing emerging technologies—particularly AI solutions—to drive continuous improvement across our call center operations. Key Responsibilities Technical Bridge Act as primary liaison between project specialists and Business Technology teams...

The Associate Data Engineer I will help build, maintain, and optimize data infrastructure - like databases and data pipelines - that address cross-functional critical business needs. This role is expected to improve existing methods and processes by using various languages to pull and manipulate data, develop and maintain ETL pipelines, implement quality control and monitoring processes to maintain accurate data flows, maintain comprehensive documentation of process designs, test results, and pipeline configurations, etc. Responsibilities Design and develop data solutions to address business challenges. Demonstrate knowledge across a range of technologies related to programming languages, data integration, data warehousing, and data...

Purpose As a translational scientist in Precision Medicine Neuroscience bridges basic brain and nervous system research and clinical applications, focusing on developing biological and disease insights for neurological and psychiatric disorders. Responsibilities Uncover neurobiological mechanisms of disease that elucidate patient subtypes; mechanisms of action, response, or resistance, and advance the development of novel interventions. Develop testable hypotheses related to neurobiological pathways, neuronal circuitry, cognitive or behavioral domains, or functional markers of disease or patient subtypes that will advance pipeline and disease area goals. Collaborate with PMed DAS leads and other functional leads, develop and execute / drive execution of operationally-sound...

Responsible for the design, implementation, integration and maintain automation systems across manufacturing operations. Responsible for moderate to complex configuration and programming of Operation Technology (OT) Systems as per AbbVie change management procedures for the manufacturing process, utilities and Facilities Control Systems. This role is responsible for leading small to medium-sized automation projects to assure project is implemented as per project schedule. This role provides technical support and system troubleshooting for systems and\or areas assigned to this position. Responsible for the administration and maintenance of assigned OT systems as per applicable departmental procedures. Responsibilities Develops moderate to complex control configuration or...

Leads the direction, planning, execution, and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in and may lead cross-functional teams to generate, deliver, and disseminate high-quality clinical data supporting overall product scientific and business strategy. Responsibilities Leads and demonstrates ownership of the design and implementation of multiple clinical development programs (or one large, complex program) in support of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations, and emerging issues. Oversees project-related education of investigators, study site personnel, and...

The Director, Inflation Reduction Act Strategy & Planning is business-critical role at AbbVie, created in response to the significant impact of the Inflation Reduction Act (IRA) on the pharmaceutical industry. This director will act as a subject matter expert, providing strategic direction and cross-functional leadership to help AbbVie proactively manage IRA-related risks and opportunities for both current commercial brands and future pipeline products. Key Responsibilities Partner closely with Commercial Therapeutics, US Market Access, Global Commercial Development (GCD), Finance, Government Affairs, and Legal to understand and dissect IRA’s potential effects on individual brands and pipeline assets. Be the subject matter expert...

This role is field-based and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience. Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations. Responsibilities Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. in order to meet or exceed...

The Immunology Discovery Therapeutic Area is seeking an accomplished and experienced Scientist to lead the Immune Cell Depletion Group within the Immune Reset Therapeutics Discovery team based in Cambridge MA. In this role you will lead a multidisciplinary team of highly talented scientists with experimental, technical and scientific expertise in cellular depletion approaches. The candidate should have a demonstratable track-record in this scientific discipline alongside a strong knowledge of preclinical drug discovery spanning target discovery / validation through to GLP toxicology phases. The ability to effectively collaborate and deliver results across multi-disciplinary line functions both internally and with external leading...

Allē Customer Experience Representatives (CXR) serve as first-line representatives responsible for handling inbound call, chat and email inquiries and act as subject matter experts regarding Allergan Aesthetics’ premier consumer loyalty program. Representatives are responsible to assist patients, health care providers and their staff, internal sales representatives and AbbVie Employees with navigating all aspects of the Allē Program. Under general supervision, Customer Experience Representatives handle customer requests in a timely, accurate and professional manner. Allē CXR’s foster the growth of a strong customer base through creating positive interactions and building strong relationships. Responsibilities Multi-Channel Support Provide excellent service through phone,...

Overview The Marketing Operations, Senior Manager works cross-functionally to project manage the review process for advertising and promotional materials for approved drug and/or device products. In addition, the Senior Manager is responsible for identifying and leading specific Marketing Operations individuals, function(s) and/or special projects, required to achieve the designated brand(s) objectives. The Senior Manager act as a Marketing Operations subject matter expert for the PRC (promotional Review Committee) review process and is responsible for ensuring the process efficiency involving Medical, Legal, Regulatory, and Compliance teams, while conforming with company policies and procedures. RESPONSIBILITIES People/team mentoring and coaching. Recruit, coach and...

An engineering professional that works with project owners, subject designers/engineers and other project team members to plan, and complete tasks associated with commissioning, qualification and validation of new and modified equipment, facilities, utilities, product, processes etc.in line with project, operations and quality objectives. Level of responsibility and performance is commensurate with grade level. The main objective is to establish evaluation, testing and documentation for risk management, commissioning and validation applying product and regulatory requirements and risk management to result in robust, high quality products. This includes optimizing systems that support the work in and around this area of responsibility. Responsibilities...

We are seeking a highly motivated in vivo electrophysiologist who will design, execute, and communicate novel multi-disciplinary research in a highly collaborative Neuroscience research team. Primary responsibilities of the successful candidate will be to apply cutting-edge single unit or multi-unit neuronal recordings to advance our Migraine and Pain programs. This effort will support the identification and development of novel therapeutics. Key Responsibilities Include Guide the use of in vivo electrophysiological techniques, and interacting with project teams to advance programs based on data Support mechanistic understanding of novel targets and evaluate related molecules to advance our Neuroscience pipeline Opportunities to contribute...

Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we’re making better health outcomes easier to achieve. Hims & Hers is a public company, traded on the NYSE under the ticker...

We are seeking a Principal Scientist, DS Process Development & Manufacturing, to join our growing Drug Substance group at GenerateBiomedicines. This role will support monoclonal antibody (mAb) drug substance development with a strong MS&T focus, bridging process development, scale-up, tech transfer, and GMP manufacturing execution. The position offers broad exposure across upstream and downstream operations, CDMO management, and quality systems. Here's how you will contribute Support Drug Substance process development and manufacturing activities (e.g., upstream expression, purification, UF/DF, viral clearance) Design and execute scale-up, process characterization, and PPQ-enabling studies Own tech transfer and support GMP campaigns at CDMO (person-in-plant support...

We are seeking an experienced Manager, Field Applications, EMEA who will play a pivotal role supporting our growing customer base in the EMEA region. This role will support a team covering one half of EMEA. This is an incredible opportunity for someone who is passionate about seeing customer success and winning for the company. We are looking for candidates with a solid background in NGS sample and library prep workflows as well as cell biology. The hired candidate will need to be physically located in the territory and be willing to travel frequently to customer sites. This role will report...

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop...

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop...

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop...

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop...

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop...

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop...

The Associate Revenue Cycle Analyst is responsible for investigating and resolving complex front-end billing issues that impact claim acceptance and reimbursement. This role focuses on EDI rejections, insurance verification, and claim submission errors to ensure claims are submitted accurately and accepted by payers. Job Responsibilities Serves as a source of knowledge for front end billing and claim rejections. Performs analysis, identifies trends, presents opportunity areas, and prioritizes initiatives for performance improvement for the designated revenue cycle function. Assist with developing appropriate workflows and tracking for the designated revenue cycle function. Establishes an ongoing working relationship with other departments impacting...

Location The territory for this role is Detroit East, MI We are currently looking for a Clinical Field Specialist (CFS) to join our Women's Health sales team! The CFS will drive revenue growth and market expansion through direct engagement with individual MFMs and OB/GYNs. This role focuses on building and maintaining strong relationships, while developing and executing strategic business plans that accelerate revenue growth. The CFS will support both established and newly launched products, providing clinical expertise, educational support, and hands-on training in technical product applications. PRIMARY RESPONSIBILITIES Increasing revenue and driving market development through direct sales to individual...

Director, Sales Strategy & Analytics The Director, Sales Strategy & Analytics is a high-impact individual contributor responsible for leading cross-functional initiatives that drive performance across Oncology and Strategic Accounts commercial teams. Operating within a complex oncology environment shaped by a multi-product portfolio and matrixed sales organization, this role will design and optimize scalable commercial infrastructure across Salesforce (SFDC), business intelligence platforms, and advanced analytical tools, including AI-enabled capabilities. This leader will combine strategic thinking, technical depth, and executive influence to enable data-driven decision-making, improve coordination across commercial functions, and drive sustained performance improvement. Key Responsibilities Strategic Initiatives & Commercial...

POSITION SUMMARY The role of Patient Coordinator will be central to the success of the Renasight product line. This position will be focused on growing the relationship between Natera and its patients to ensure timely management of testing. Core responsibilities include collaborating with Nurse Coordinators to increase revenue and drive market development through direct sales by being the key contact for patient needs. The Patient Coordinator will accomplish this by being the patient advocate within Natera. PRIMARY RESPONSIBILITIES Work with assigned customer care team to maintain & support existing customers. Assess the needs of patients with a focus on customer...

Principal Software Engineer Location South San Francisco, CA preferred; Remote optional Job Type Full-time About the Role We're seeking a Principal Software Engineer to join Natera's R&D Platform Infrastructure team. The team builds the cloud infrastructure, workflow platforms, and data platforms that R&D uses to do its science — including a Kubernetes-based workflow execution platform, a custom R&D LIMS system, and a set of supporting tools that routinely handle production-scale workloads. This is a senior technical role. You'll own the full architecture, implementation, and delivery of large projects across our platform. You'll partner with the team lead on roadmap...

POSITION SUMMARY We are seeking a Staff Machine Learning Scientist – Translational AI to provide technical leadership at the intersection of deep learning foundation models, computational biology, and molecular diagnostics. This ownership role drives the architecture and validation of genomic, transcriptomic, and multimodal sequence models to accelerate patient stratification, target identification, and therapeutic monitoring across our cell-free DNA (cfDNA) and multi-omic platforms. This Staff-level position operates with broad technical autonomy, driving modeling strategy across multiple concurrent portfolios while maintaining direct execution responsibilities in model compilation, scaling, and testing. Working within a builder framework, you will align across AI Research, Bioinformatics,...

POSITION SUMMARY Natera is a global leader in cell-free DNA testing. We measure fetal, tumor, or donor cfDNA at the molecular level to help inform personalized health care decisions with a non-invasive test. We are looking for a highly motivated Staff Scientist to join Natera’s Oncology Product Development Team. We are looking for a seasoned candidate with experience in next generation sequencing (NGS) assay development who enjoys solving challenging and complex problems in a fast-paced environment. The ideal candidate is self-motivated and effectively works around unknowns to move the needle in the development, launch, and support of the highest quality...

LOCATION The territory for this role is the New England area which includes ME, NH, VT, MA, Upstate NY, CT, RI L We are hiring a Women’s Health Strategic Account Manager (SAM) to join Natera! The Strategic Account Manager works with the local women’s health sales team to develop and execute strategies to increase Natera testing in IDNs, large hospital systems and Academic Medical Centers. This role involves internal collaboration, leading without authority, and forming relationships with key senior level influencers within health systems. PRIMARY RESPONSIBILITIES Educate and recruit Strategic Accounts and Lab Partners to utilize Natera’s women’s health...

Vice President, Laboratory Operations About the Role As Vice President of Laboratory Operations, you will drive strategic vision and operational excellence across our laboratory. Collaborating closely with other leadership, you will champion operational needs, spearhead cross-departmental initiatives, and optimize key performance indicators (KPIs) to enhance quality, capacity, turnaround time (TAT), and cost of goods sold (COGS). You will serve as the primary point of contact for delegated products, fostering strong partnerships and delivering clear, concise updates to executive leadership. This role demands a strategic leader who can contribute to budget planning, monitor financial performance, and ensure efficient workflow, customer satisfaction,...

Partner Data Analyst - Life Science Partnerships This Opportunity This Partner Data Analyst position is a high impact, customer-facing role that requires a diverse set of skills spanning technical execution, applied research methodology, and relationship management. You will work directly with life sciences partners to translate research questions into analytical approaches, execute studies using real-world Electronic Health Record (EHR) data (~120M+ patients), and guide customers in best practices for real-world evidence generation. You will play a key role in advancing customer research by helping shape analytical approaches, ensuring methodological rigor, and driving projects forward from question to insight....

About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer’s disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we’re here to be their difference. Please note that this position can be...

A Rare Opportunity to Shape the Future of Genomics Join a team of brilliant, passionate innovators determined to transform healthcare. At BillionToOne, we've built a category-defining, publicly traded company on Nasdaq where transparency fuels trust, collaboration drives breakthroughs, and every contribution moves the needle on our mission to make life-changing diagnostics accessible to all. We don't just aim for incremental improvements; we build products that are 10x better than anything that exists today. Our scientists, engineers, sales executives, and visionaries are united by an unwavering commitment to changing the standard of care in prenatal and cancer diagnostics. This is where...

As an Associate Director, Field Medical Affairs (Medical Science Liaison) responsibilities include engaging in the exchange of scientific data and other medical and/or scientific information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. We expect you to demonstrate a thorough understanding of Neurology aligning with our strategic medical plans. The position will bring relevant insights from the field on research developments, treatment landscape and other opportunities shaping our medical strategy. You will be considered a scientific and clinical expert on our current and future Neurology assets. Territory Cincinnati OH, Southern VA, Eastern KY, WV, TN, NC, SC A typical...

As an Associate Director, Field Medical Affairs (Medical Science Liaison) responsibilities include engaging in the exchange of scientific data and other medical and/or scientific information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. As a scientific expert in your territory, you will demonstrate a thorough understanding of Neurology aligning with our strategic medical plans. The position will bring relevant insights from the field on research developments, treatment landscape and other opportunities to shape our medical strategy. You will be considered a scientific and clinical expert on our current and future Neurology assets. Territory GA, AL, FL, PR A typical...

The main responsibility of the HCP Contract Specialist is to collaborate closely with internal and external stakeholders to facilitate the efficient and timely progression of HCP consultancy agreements and providing oversight throughout lifecycle of the agreements. A typical day in this role loos like Acting as a delegate for the HCP contracting Sponsor, ensure that all business-facing and other process requirements / information is available and entered in the systems completely and in a timely manner to ensure efficient progression of all assigned HCP contracts Diligently manage all HCP contracting tasks and activities assigned to the HCP Sponsor, ensuring their...

As an Associate Director, Field Medical Affairs (Medical Science Liaison) responsibilities include engaging in the exchange of scientific data and other medical and/or scientific information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. We expect you to demonstrate a thorough understanding of Neurology aligning with our strategic medical plans. The position will bring relevant insights from the field on research developments, treatment landscape and other opportunities shaping our medical strategy. You will be considered a scientific and clinical expert on our current and future Neurology assets. Territory TX, AR, MS, LA A typical day may include the following Establish,...

Specific Education & Experience Requirements 12+ years of experience and a BS in a relevant scientific discipline. 12+ years of relevant experience and a MS degree. 14+ years of experience and an RN (2 or 3 year certificate) Prior experience leading and overseeing oncology clinical trials with a minimum of 5 years’ experience in the design and delivery of Phase 1 first in human (FIH) oncology clinical trials Specific Job Responsibilities Provides leadership and therapeutic expertise for the successful management of international clinical trials (Phase I - IV) across multiple indications through clinical study teams and through the use of...

Associate Director, Statistical Programming (Macro Support) Job Summary Leads statistical programming tool development (e.g., SAS macros, automation solutions) supporting multiple studies and/or workstreams and ensuring delivery of high-quality, scalable tools aligned with Clinical Data Science and Statistical Programming standards. Contributes to departmental strategies, tools, and infrastructure that enable efficiency and consistency across Statistical Programming. Key Responsibilities Leadership & Delivery Accountable for planning and delivery of tool development aligned with study and business timelines. Influences design, development, qualification, and maintenance of SAS macros and related tools used across multiple studies or initiatives. Acts as a project or functional lead for statistical...

Gilead is looking for an Executive Director - Gilead Asset Team Leader (GATL) – Inflammation Partnership —a role where your work can help advance life‑changing scientific innovation and meaningful patient impact. Jointly reporting to the Commercial and Development Therapeutic Area Heads, the Gilead Asset Team Leader (GATL) is an enterprise leader responsible for leading the cross-functional asset team and shaping the asset vision, strategic direction, and lifecycle plan (LCP) including across multiple indications and drug combinations . Serving as the primary liaison for senior leadership within the governance model, the GATL drives collaboration across Gilead, engaging diverse stakeholders involved in...

At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers. We set and achieve bold ambitions in our fight against the world’s most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come. As the Executive Director, Global Commercial Excellence Lead, at Gilead you will lead enterprise-wide transformation of global commercial capabilities to fundamentally improve...

The Director, Quality Compliance and Audits (QCA ) reports to the Executive Director, Quality Compliance & Audits and provides strategic leadership and governance for Gilead’s global GMP and GDP audit program. This role leads and develops a team of auditors and ensures consistent, high‑quality audit execution across Gilead’s global manufacturing and supply network, including internal manufacturing facilities, external contract manufacturers, laboratories, suppliers, distributors, and other third‑party partners. The Director is accountable for oversight of the end‑to‑end audit lifecycle, including development and execution of the annual audit plan, and ensures audits are performed as systematic, independent, and objective assessments of compliance...

POSITION OVERVIEW The Executive Director, Head of Precision Medicine Regulatory is responsible for defining and leading enterprise-wide regulatory strategy for precision medicine, including companion diagnostics (CDx), in vitro diagnostics (IVD), and biomarker-driven development across all Gilead therapeutic areas. This role ensures seamless integration of diagnostic and therapeutic development strategies from early discovery through global registration and commercialization, while maintaining direct accountability for regulatory strategy and execution of CDx/IVD programs. The position operates at the intersection of enterprise leadership, technical regulatory expertise, and operational execution to enable scalable, compliant, and innovative precision medicine across the Gilead and Kite portfolios. You will...

At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers. We set and achieve bold ambitions in our fight against the world’s most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come. As a Principal Scientist, Analytical Operations at Gilead you will act as a Quality Control (QC) Lead will be responsible for the...

As a Manager, IT Risk and Compliance – DOJ Data Security Program , at Gilead you will ... Th e Manager, DOJ Data Security Program is part of Gilead’s Security Risk & Compliance (SRC) Governance team and leads efforts to ensure ongoing compliance with Department of Justice (DOJ) Data Security Program (DSP) requirements. This role partners across IT, Security, Legal, Privacy, Compliance, and business teams to ensure controls are effective, risks are managed, and the organization maintains a continuous state of audit readiness. The position combines regulatory knowledge, control oversight, and cross-functional collaboration to drive a proactive compliance program. The...

#LI-Onsite Location Cambridge, MA This role is based in Cambridge, MA, and does not have the ability to be located remotely. The Novartis BioMedical Research Oncology Disease Area is seeking an experienced scientist to join the Target Biology and Discovery (TBaD) group. The mission of our group is to uncover novel therapeutic targets and effective modalities to benefit cancer patients. By leveraging cutting-edge technologies, innovative screening approaches, and in-depth mechanistic studies, the team initiates the crucial first steps in bringing new oncology medicines to the clinic. Key Responsibilities Apply modern chemical genetics approaches to identify and validate novel targets...

#LI-Onsite Location Cambridge, MA This position is located in Cambridge, MA and does not have the ability to be located remotely. Please only apply if this area is accessible to you. Over 40 therapies in the clinic! NIBR Oncology strives to reimagine medicines for cancer patients through a combination of treatment approaches including targeted therapies, immunotherapies, CAR-T, and radioligand therapy. NIBR is seeking an in vivo scientist to join our Oncology Pharmacology team in Cambridge, MA. The successful candidate will join a dynamic, multi-disciplinary team and play a key role in the development and application of in vivo models for...

Director & Group Head (Applied AI) #LI-Hybrid Location Cambridge, USA Relocation Support This role is based in Cambridge, USA. Novartis is unable to offer relocation support please only apply if accessible. Novartis has embraced a bold strategy to drive a company-wide digital transformation. Our objective is to position Novartis as an industry leader by proactively adopting digital technologies that foster innovative approaches to hasten drug discovery and development. By utilizing both internal and external R&D data with the power of data science, predictive models, generative AI, and machine learning, our objective is to identify new targets, create more effective therapeutic...

#LI-Remote This is a field-based and remote opportunity supporting key accounts in an assigned geography. Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible to you. Company will not sponsor visas for this position. As a Territory Account Specialist (TAS), you’ll lead with purpose – crafting personalized experiences that reflect the unique needs of each account and Health Care Provider (HCP). Acting as the primary point of contact, you’ll build meaningful connections, identify shared priorities, and navigate solutions that link customers to Novartis resources – all with the goal of improving...

In this role you will support the manufacturing team and provide technical expertise to regularly draft and revise documents such as Standard Operating Procedures (SOP'S), protocols, technical reports, and training material in a GMP regulated environment that supports the manufacturing process. Develop, review, and update technical content including but not limited to standard operating procedures, work instructions, risk assessments, protocols & reports for manufacturing team. Provide technical and clerical support to the manufacturing team in the preparation of documentation, collation of data and tracking of technical documents. Liaise with manufacturing team and other cross functional departments regarding documentation changes in...

Senior Associate, Outbound Warehouse Operations Amgen Advanced Assembly and Final Product Operations What you will do In this vital role, you will support outbound warehouse operations responsible for the distribution and shipment of finished goods while ensuring compliance, operational efficiency, and service excellence. Reporting to the Outbound Warehouse Manager, you will play a key role in daily warehouse execution, system transactions, inventory management, and cross-functional coordination supporting the Amgen Ohio (AOH) site. The Senior Associate, Outbound Warehouse Operations, will support outbound shipping activities, warehouse systems, inventory movements, and process improvements to ensure accurate and timely delivery of products to...

Quality Control Specialist, Microbiology What you will do In this vital role, you will provide technical and operational leadership for the QC Microbiology and Environmental Monitoring laboratories, leading microbial identification activities, environmental monitoring investigations, and laboratory operations in a highly dynamic, team-oriented environment. In this role, you will be responsible for Lead microbial identification activities, organism assessments, and support routine and non-routine microbiological testing. Provide leadership for microbiology laboratory operations, coordinate daily priorities, supervise laboratory staff, and support weekend laboratory operations. Own and lead complex microbiological investigations, deviations, environmental monitoring excursions, and contamination events, including root cause analysis, risk...

Senior Associate Quality Assurance What you will do Let’s do this! Let’s change the world! The Sr. Associate Quality Assurance position supports Amgen’s Quality Assurance program under the Plant QA organization providing daily oversight of the Drug Product manufacturing areas. Under general supervision, the role provides support and quality oversight of our Drug Product Manufacturing facility, ensuring the execution of our processes, procedures, and use of quality systems aligns with regulatory requirements. Duties include but are not limited to Purposeful presence on the manufacturing floor (Form/Fill Grade 8 Gowning), 100% Manual Visual Inspection support, ASP/AQL performance, and QA Oversight Assessments...

Executive Director, Facilities & Engineering (ARI Site Facilities & Engineering) What you will do In this vital role as Executive Director, Facilities & Engineering, you will lead the organization responsible for supporting GMP manufacturing operations (24x7x365) while optimizing asset lifecycle management across the site for biologics drug substance manufacturing, warehousing, central utilities, quality control laboratories, process development laboratories, and administrative facilities. The Executive Director, Facilities & Engineering (F&E) reports directly to the Vice President, Amgen Rhode Island (ARI) Site Operations and the Facilities & Engineering organization includes the following functional areas Facilities, Maintenance & Utilities; Process & Equipment Engineering;...

ASSOCIATE TECH ENGINEERING (NIGHT SHIFT) What you will do In this vital role you will support the performance, maintenance, and continuous improvement of manufacturing systems and equipment that power the production of life-changing therapies. Specific responsibilities include but are not limited to Support automated systems, vision system, automatic equipment, and mechanical equipment, demonstrating a strong understanding of how they interconnect and function. Use systems like MAXIMO to manage tasks, maintenance activities, and equipment logistics efficiently. Assist in equipment installation, updates, and maintenance alongside vendors and internal teams. Follow cGMPs, SOPs, and safety protocols rigorously, ensuring accurate and timely documentation...

Senior Scientist What you will do In this vital role you will join the Safety Pharmacology Sciences team. The successful candidate will serve as a subject matter expert in nonclinical safety pharmacology, partnering closely with project teams to develop and execute integrated safety pharmacology strategies that support discovery, candidate selection, IND-enabling packages and regulatory submissions. This role will require strong scientific judgment, regulatory awareness, cross-functional collaboration, and the ability to translate complex nonclinical safety pharmacology data into clear, actionable recommendations for project teams and governance forums. The Senior Scientist will work closely with Safety Pharmacology Sciences colleagues to shape...

Senior Associate, Coverage & Pricing Strategy, Inflammation What you will do In this vital role you will be a key member of the U.S. Value & Access, Coverage and Pricing organization responsible for supporting the development and implementation of a plan of action for pricing, reimbursement, and contracting strategy to improve payer coverage within pricing goals. The Senior Associate (reporting to a Senior Manager) will help develop and implement coverage and pricing strategy, through quantitative and qualitative analysis, across the inflammation portfolio. In this dynamic environment, this role interacts cross functionally with Market Access, Value Marketing, Patient Access, Ecosystems...

Manager Inbound Warehouse Process Amgen Advanced Assembly and Final Product Operations New Albany, Ohio What you will do In this vital role, you will be part of the Supply Chain team and report to the Senior Manager, Supply Chain over all Warehouse operations, and you will participate in multiple cross-functional initiatives for Amgen Ohio (AOH) leading to the improvement of the overall planning process utilizing enterprise-wide programs. In addition, you will organize, drive, and/or support the identification and implementation of related Warehouse systems and processes. The Manager, Inbound Warehouse Process will be the systems and process expert for Amgen’s...

Senior Manager, CV-Repatha Omnichannel Orchestration, Modular Content Operations, Search / GEO & AI Answer Engine What you will do The Senior Manager, CV / Repatha Omnichannel Marketing evergreen posting is designed to identify exceptional candidates for multiple Senior Manager opportunities supporting the CV / Repatha omnichannel team. Candidates may be considered for one or more roles across Omnichannel Orchestration, Modular Content Operations, and Search / Generative Engine Optimization (GEO) & AI Answer Engine. These roles will help CV / Repatha move from channel-by-channel execution to a more audience-first, signal-informed, content-enabled, and measurable omnichannel operating model. The selected leaders will partner...

Sr Associate Supply Chain- Warehouse Technical Operations What you will do In this vital role, you will be part of the Supply Chain team and report directly to the Inbound Process Manager, and will participate in multiple cross-functional initiatives for Amgen Ohio (AOH) leading to the improvement of the overall planning process applying enterprise-wide programs. You will organize, drive, and/or support the identification and implementation of related Warehouse systems and processes. The Sr. Associate Supply Chain will assist the Manager to become the systems and process expert for Amgen’s Warehouse systems and sub-systems. You will help develop and provide...

Associate Director, Finance Technology, AI Data & Innovation What you will do In this vital role you will lead the development and execution of the CFO organization’s digital, AI, data, and innovation agenda. This role will partner closely with Finance senior leaders, Digital/Technology, Data, Cybersecurity, Compliance, and cross-functional stakeholders to identify, prioritize, and deliver technology-enabled solutions that improve Finance productivity, decision-making, operational effectiveness, and enterprise value. The role will serve as a strategic connector between Finance business needs and technology capabilities, helping translate priorities into scalable solutions, responsible AI use cases, data-driven insights, and new ways of working. This...

SAP Principal Architect - Transportation Management What you will do In this vital role you will be a thought leader who helps to drive Amgen’s digital and innovation ambitions. Leveraging SAP S/4 TM architecture standards and through alignment of digital strategy and solutions to business outcomes, you will optimize the value of our technology investments, creating new value for our staff, our business partners, our shareholders and most importantly – our patients. As a SAP TM Solution Architect you will Be accountable for helping drive the successful design, architecture, build, test and implementation SAP S/4 Transpiration management solution across...

Venue Strategy Manager, Global Meetings Management What you will do Let’s do this. Let’s change the world! In this vital role you will lead our venue strategy, hotel sourcing, contracting, and supplier relationship management for Amgen's U.S. Commercial internal meetings portfolio including large sales meetings, incentive programs, and executive leadership events. 1. Venue Strategy & Planning – 25% In support of the business objectives, partner with internal stakeholders on venue strategy recommendation and execution for U.S. Commercial internal meetings, including national sales meetings, POAs, launch meetings, leadership summits, training programs, incentive programs, and other internal events. Partners with business and...

In this vital role, you will be part of the Supply Chain team and report to the Senior Manager. You will participate in multiple cross-functional initiatives for Amgen Ohio (AOH) leading to the warehouse quality process applying enterprise-wide programs. In addition, you will organize, drive, and/or support the identification and implementation of related Warehouse systems and processes. This role is also responsible for identifying, establishing, modeling, and monitoring key performance measures that will ensure the achievement of Best Practices across Amgen sites. The Manager, Warehouse Quality Systems, will serve as a key representative on various cross-functional task forces and teams...

In this vital role you will be representing Tavneos to physicians and healthcare professionals, playing a key role in establishing product demand and delivering comprehensive account management within a designated territory. You will serve a central point of contact, response for educating medical professionals and external stakeholders on disease state awareness and product information to support optimal patient care. As a SAM, you will drive product utilization while identifying and addressing the unique needs of each account. This includes building and maintaining strong relationships with healthcare providers, coordinating cross-functional field teams, and executing aligned strategies to ensure access, education, and...

Senior Specialty Representative – Respiratory – Rochester, NY Live What you will do Tezspire In this vital role you will be the liaison to our customers by providing clinical knowledge of our products to medical professionals. Amgen's medicines treat serious illnesses and our research address diseases with a limited number of treatment options. With a robust and differentiated pipeline, Amgen remains committed to advancing science to dramatically improve people's lives. As a values-based organization with a powerful sense of shared purpose toward our mission to serve patients, we are actively searching for a Senior Specialty Representative to deliver on...

Associate Quality Control - Incoming What you will do In this vital role the successful candidate will work with a team responsible for the Incoming Quality Control sampling and inspection processes of primary/secondary components, devices and raw materials. In addition, will be responsible for raw material sample shipments, testing and batch record's review per standard operating procedures or guidelines. Will also work cross-functionally to support multiple customers and stakeholders including Supply Chain, Quality Assurance, Process Development, Engineering and Quality Control. Specific responsibilities include but are not limited to Complete onboarding and all required training qualifications. Perform routine sampling and...

In this role you will lead various smart manufacturing technology and computerized systems initiatives within manufacturing to support the end user on the shop floor (e.g. AR/VR Technology, MES, ERP, SCADA, Systech, Serialization). You will manage critical processes, provide technical leadership, and be accountable for designing, implementation, and validation of key business systems and digital technologies. You will support the development of master batch records, technical reports, and other Good Manufacturing Practices (GMP) documents that supports smart manufacturing technology and the production process. This role is essential for Amgen Ohio’s success and key in supporting operations towards the digital future...

Account Manager/Specialty Account Manager - TEPEZZA Live What you will do In this vital role you will be responsible for representing TEPEZZA to physicians and health care professionals, establishing product sales, and performing total territory account management. The Specialty Account Manager is responsible for providing account management support to accounts within a specific geography in the designated marketplace with a focus on issues specific to their designated accounts. The SAM acts as central account manager; responsible for driving product demand and coordinating relevant field teams to address account needs. Responsibilities Develops a comprehensive and effective territory business plan aimed...

Associate - Protein Chemistry What you will do Amgen is seeking a highly motivated Associate to join the Protein Therapeutics (PT) – Protein Chemistry team. PT is a multidisciplinary team with broad capabilities in protein engineering, expression, purification, and characterization. We are responsible for the engineering, production, assessment, and final selection of large molecule drug candidates that advance to Process Development. In this role, you will support the analysis and characterization of large molecule, therapeutic drug candidates, many of which are complex biologics. Responsibilities Analyzing and characterizing novel and complex molecules that will be the next generation of large...

Key Account Manager - Bone Health Live What you will do The Key Account Manager – Bone Health will report into the Key Account Director. Their primary responsibility is to assess and diagnose the current business environment in each of their assigned accounts in relation to Amgen products and plan/execute actions for success in these accounts. The Account Manager will work internally through the matrix team, and externally with customers to develop strong relationships for Amgen to support sales performance and brand strategies at multiple touch points and levels within complex partner organizations. Ideally, the candidate resides in the geography...

AI Senior Scientist , Rare Cancer Discovery Location Waltham, MA At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person. Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in...

In AstraZeneca's Cell Therapy division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying, and even curing some of the world's most complex diseases. We have the potential to grow our pipeline and positively impact the lives of patients around the world. We are committed to making a difference and have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. The Associate Director – Territory Operations Manager (AD-TOM) is a regional expert supporting Patient Operations and...

Senior MSL – Hematology (S. Chicago, and downstate IL) *Can be considered for MSL or SR. MSL depending on experience We're growing! Ready to join an amazing team? Do you have expertise in, and passion for Medical Affairs in Oncology ? Are you ready to make a significant impact in the field of Hematology ? AstraZeneca’s vision in Oncology is to help patients by redefining the cancer-treatment paradigm with the bold ambition to eliminate cancer as a cause of death. We are proud to work on groundbreaking science with one of the broadest and deepest Oncology pipelines in the business....

Senior Statistician II Location Boston The Senior Statistician II has sufficient experience working as a statistician in the pharmaceutical industry to be working independently on activities relating to design, delivery and interpretation, regulatory submissions and/or commercialisation. This individual is able to perform and communicate results of more technical analyses, and able to guide less experienced staff. They have the scope to develop creative statistical ideas and approaches, and to apply them in their work. Competent individual contributor with excellent cross-functional collaboration. Typical Accountabilities The Senior Statistician II will work directly within a project. The accountabilities for supporting projects directly are...

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe. Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our head office and BlueSky Hub in downtown Toronto are purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm...

Join AstraZeneca’s Oncology Business Unit (OBU) in a role where strategy meets scientific ambition. As an Associate Director, OBU Strategy, you will assist in the creation and implementation of strategies to deliver an exciting and innovative oncology pipeline. You will drive the collection of meaningful, timely, and accurate data from a wide range of internal and external sources and perform detailed analyses. Your analysis and strategic advice will drive the long-term strategy for projects across early and late-stage development and will be the foundation for investment decisions. Accountabilities Lead the collection and analysis of data to inform project strategies and...

Opportunity Medical Director, Senior Patient Safety Physician Based in Gaithersburg, USA As a Medical Director, Senior Patient Safety Physician , you are a senior leader within Patient Safety and play a key role bringing deep clinical understanding and judgement in benefit risk assessments for AstraZeneca products. You also have a role in shaping the culture of the department; and will act as a coach and mentor to more junior Patient Safety staff. You will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and regulatory requirements. We encourage you to closely follow medical developments within assigned areas to...

Set up and operate manufacturing processes and ensure compliance with safety and Good Manufacturing Practice (GMP) standards. Responsibilities include handling materials, packing products, managing production waste, and keeping work areas safe and clean. Accountabilities - Work as part of a team to help achieve production and quality goals. - Ensure that materials and products meet required specifications and production schedules. - Set up, operate, and support routine maintenance of manufacturing equipment according to established parameters. - Assist in resolving routine production or equipment issues, advancing more complex problems as needed. - Follow established safety, health, environmental, sustainability and GMP/quality standards...

Senior Assay and Data Specialist Are you ready to push the boundaries of science and transform the lives of patients? Join the Assays Profiling and Pharmacology (APP) team at Gaithersburg within Biologics Engineering (BE), where we develop high throughput, robust, and innovative assay platforms for characterizing novel biologics. Collaborating with AstraZeneca’s therapeutic area functions, we provide cutting-edge drug discovery capabilities to support our expanding portfolio. As a Senior Assay and Data Specialist, you'll work alongside wet lab assay scientists, automation engineers, and data scientists to build interconnected workflows. You'll be the primary assay and data hybrid scientist responsible for creating...

The Associate Director, Digital & Business Process Strategy leads the vision, roadmap, and value delivery of digital products that span PAS ‑ X , Tulip (MES), data historians, and LIMS within AstraZeneca’s manufacturing network. This role sits in the Digital & Business Process Strategy team and partners with Operations, Quality, Global IT, Data & AI, Supply Chain and Site teams to modernize data flows, improve Right ‑ First ‑ Time , and enable compliant, data ‑ driven decision making from shop floor to enterprise. You will be based in Rockville, MD and report to the Senior Director of Digital &...

At AstraZeneca, we turn ideas into life-changing medicines. Working here means thinking big and working together to make the impossible a reality. We’re focused on the potential of science to address the unmet needs of patients around the world. We commit to those areas where we think we can really change the course of medicine and bring big new ideas to life. At AstraZeneca, we are taking bold action on climate because we recognize the connection between healthy people and a healthy planet. As part of our flagship Ambition Zero Carbon program, we have committed to a fully electric vehicle...

As a Global Product Planner for Cell Therapy at AstraZeneca, you will be instrumental in driving the strategic planning and execution of our innovative cell therapy products across the global supply chain. This role offers a unique opportunity to combine your expertise in supply chain management with a passion for making a difference in patients' lives. You may be based in Tarzana, CA or Gaithersburg, MD and will report to the Senior Director, Supply Chain Planning. What you will do End-to-end Tactical Planning Take ownership of the end-to-end tactical planning process for the assigned cell therapy product portfolio, ensuring synchronization...

Associate Director, External Quality Location Boston, MA Hybrid 3 days/week Fusion Pharmaceuticals, a member of the AstraZeneca Group, is a clinical-stage oncology company focused on developing next generation radio conjugates (RCs) as precision medicines. Fusion has multiple pipeline programs entering early FIH trials. In addition, Fusion is pursuing combination programs between RCs and other therapeutic modalities including DNA Damage Response Inhibitors (DDRis) and immune-oncology agents. To support these programs, Fusion has a fully operational radio conjugate manufacturing facility. It is brand new and GMP compliant to meet the demand for our growing pipeline of RCs. AD, External Quality –...

In AstraZeneca's Cell Therapy division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying , and even curing some of the world's most complex diseases. We have the potential to grow our pipeline and positively impact the lives of patients around the world. We are committed to making a difference and have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. This role is part of the Cell Therapy Supply Chain team tasked with supporting critical...

AstraZeneca, a global leader in biopharmaceuticals, is committed to discovering and delivering innovative therapies that transform patient outcomes. We are seeking a dedicated, hands-on Associate Principal Scientist or Principal Scientist to join our Immunology Cell Therapy Discovery team. This role will provide scientific and technical leadership across discovery initiatives with a dual emphasis on immune mediated diseases and computational innovation, with particular focus on bioinformatics, data science, and AI architecture to accelerate cell therapy discovery. The successful candidate will operate at the interface of immunology, computational biology, and AI-enabled research, partnering across multidisciplinary teams to advance target identification, patient stratification,...

Senior MSL – Hematology ( M I, IN, and KY) *Position could be either Senior MSL or MSL level depending on experience We're growing! Ready to join an amazing team? Do you have expertise in, and passion for Medical Affairs in Oncology ? Are you ready to make a significant impact in the field of Hematology ? AstraZeneca’s vision in Oncology is to help patients by redefining the cancer-treatment paradigm with the bold ambition to eliminate cancer as a cause of death. We are proud to work on groundbreaking science with one of the broadest and deepest Oncology pipelines in...

Join a collaborative, tech-enabled team using data, analytics, and current engineering to boost asset performance and sustainability. You’ll turn metrics into action, lead a high-performing team, and deliver projects that strengthen infrastructure and reduce environmental impact—shift after shift. What you’ll do Facilities and utilities Keep campus-critical systems running through preventive, predictive, and corrective maintenance; ensure uninterrupted utilities for cGMP operations and respond to BMS alarms 24/7. Maintenance excellence Build and optimize PM programs, follow KPIs, and lift uptime and asset health. Work management Partner with Planning and Scheduling; drive accurate CMMS (SAP) data and effective work execution. Materials and spares...

The Search and Evaluation Associate Director, Respiratory & Immunology is a key role in Biopharmaceuticals R&D at AstraZeneca, supporting global Business Development initiatives with a direct impact on the scientific strategy and portfolio. The S&E group is responsible for driving search efforts for external innovation throughout the Biopharma R&D R&I community and conducting technical due diligence activities that ensure an in-depth understanding of investment opportunities and provide effective decision-making tools for the organization. In this role, you will have a major impact on the strategic development of Biopharmaceuticals R&D, R&I, ensuring that the portfolio is delivered and that the science,...

The Senior Marketing Manager, Non-Personal Promotion (NPP) TRUQAP will be responsible for leading execution of HCP digital and non-personal marketing efforts in the US market. This role will help translate TRUQAP brand strategy into high- impact omnichannel programs that engage healthcare professionals, support appropriate patient identification, and strengthen TRUQAP’s position in an increasingly competitive oncology marketplace. The Senior Marketing Manager will work closely with the broader TRUQAP team and cross-functional partners across Market Access, Sales, Medical, Regulatory, Legal, Compliance, Insights, Analytics, and agency partners to ensure aligned, compliant, and effective execution. This position will report to the US Head of...

At AstraZeneca's, we follow the science to explore and innovate. We are working towards treating, preventing, modifying , and even curing some of the world's most sophisticated diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. We are committed to making a difference and have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. The Director of Project Management Office, Cell Therapy Technical Operations is a highly strategic...

Join AstraZeneca’s Oncology Business Unit (OBU) in a role where strategy meets scientific ambition. As Director, OBU Strategy, you will translate cutting-edge science into bold, evidence-based portfolio choices—partnering with R&D and commercial leaders to shape the trajectory of our innovative pipeline and accelerate medicines to patients. This is a high-impact, highly visible opportunity to lead market-shaping analyses, challenge assumptions with rigor, and influence senior decision-making across all stages of development. If you thrive in fast-paced environments, bring deep oncology insight, and are motivated by clear societal impact, this role offers a platform to drive meaningful outcomes for patients and the...

Você está pronto(a) para fazer a diferença no setor farmacêutico? Como Propagandista Vendedor, você terá a oportunidade de gerenciar seu território, propondo soluções inovadoras que impactem diretamente na performance do setor. Este é o momento de aplicar seus conhecimentos técnicos e habilidades de comunicação para promover nossos produtos e garantir que eles cheguem aos pacientes que mais precisam. Responsabilidades Gerenciar o território propondo soluções que impactem na performance do setor. Planejar e executar o trabalho de promoção médica e visitação PDV, para garantir a geração da demanda e assegurar a conversão em venda na farmácia. Aplicar conhecimentos técnicos dos produtos...

Location Wilmington Hybrid Policy 3 days a week onsite At AstraZeneca, we turn ideas into life-changing medicines. Working here means thinking big and working together to make the impossible a reality. We’re focused on the potential of science to address the unmet needs of patients around the world. We commit to those areas where we think we can really change the course of medicine and bring big new ideas to life. Join us as Senior Director, Marketing - Dyslipidemia in Wilmington for the US Bipharma CVRM therapeutic area where you will play a pivotal role in channeling our scientific capabilities...

At AstraZeneca, we turn ideas into life changing medicines. Working here means being thinking big and working together to make the impossible a reality. We’re focused on the potential of science to address the unmet needs of patients around the world. We commit to those areas where we think we can really change the course of medicine and bring big new ideas to life. At AstraZeneca, we are taking bold action on climate because we recognize the connection between healthy people and a healthy planet. As part of our flagship Ambition Zero Carbon program, we have committed to a fully...

Use Your Power for Purpose We are seeking a highly organized, proactive, and detail-oriented Administrative Lead to provide comprehensive support to our PhRD Management Teams, Leadership Team (LT), and staff located in Andover, MA. In this vital role, you will serve as the operational anchor for our team—ensuring seamless day-to-day activities, managing complex schedules, and leading coordination efforts for facilities, IT, and HR-related processes. As a collaborative problem-solver who takes ownership of administrative workflows, your efficiency and dedication will directly enable our research and development team to stay focused on delivering breakthrough therapies that change patients' lives. If you thrive...

Pfizer US/PR Commercial Sales Founded in 1849,

The Marketing Academy is Pfizer’s capability-building ecosystem that strengthens marketing excellence through applied learning, curated programs, and shared standards—helping marketers deliver stronger performance and patient impact. Reporting to the Marketing Academy Capabilities & Strategic Platforms Lead, the Director, Marketing Academy—Curriculum Design & Excellence co-leads the End‑to‑End Execution Excellence track and ensures the Academy’s track ecosystem is coherent, scalable, and standards-aligned. As a strategic integrator across Track Leads, SMEs, Digital/MarTech partners, and enablement stakeholders, this role translates real marketer workflows into high-impact curriculum and enablement that accelerates adoption and improves marketing execution outcomes. While the scope of the role is global,...

Pfizer US/PR Commercial Sales Founded in 1849,

Use Your Power for Purpose At Pfizer, we believe that every role contributes to our mission of improving patients' lives. Whether you are involved in the design and development of manufacturing processes for products or supporting the upkeep of systems, engineering is crucial to ensuring customers and patients receive the medicines they need. By collaborating with our forward-thinking engineering team, you'll play a pivotal role in accelerating the delivery of medicines to the world. The Senior Manager, IFM Program Lead (Sanford) provides strategic and operational leadership for the site’s Integrated Facilities Management (IFM) delivery model. This role is accountable for...

Use Your Power for Purpose The Director of Innovation, Commercial Technology is responsible for establishing and advancing the short- and long-term commercial technology vision and strategy for the Global Hospital & Biosimilars (GH&B) business unit. Through rigorous market research and strategic collaboration with customers, wholesalers, third-party organizations, industry technology partners, and key opinion leaders, this role is accountable for identifying and evaluating near-term customer technology needs as well as forecasting longer-term market trends. The Director will assess which of these trends GH&B should prioritize and will develop innovative initiatives and solutions designed to differentiate our product portfolio, enhance customer convenience,...

ROLE SUMMARY Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is innovative and customer oriented . Whether you are involved in manufacturing, testing, or compliance, your contribution will directly impact patients. All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues can grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized...

Use Your Power for Purpose Our breakthroughs would not make it to the hands of patients without our dedicated and agile pharmaceutical manufacturing team. We rely on members who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always strive to improve outcomes. You will help ensure that patients and physicians have the medicines they need when they need them. What You Will Achieve In this role, you will Maintain proper documentation – batch records, check sheets, logbooks. Perform fill room setup and perform room and...

The Senior Biostatistician II will perform scientific statistical analyses in support of the company's Global Medicines Development and Affairs area with guidance and mentoring on new and complex issues. The incumbent will complete assigned work in a resourceful manner and create alternative approaches to achieve desired results. The incumbent will develop a good knowledge of related disciplines while performing Biostatistics activities with a drug developer mindset. Key Duties and Responsibilities Within assigned area, designs, develops and executes the technical/statistical infrastructure for the conduct and evaluation of clinical trials, observational studies, or real world data (RWD) investigations, including related areas/activities. Participates...

We are looking for a highly skilled and experienced Associate Director to lead Procurement Operations and Vendor Management within Vertex's BPO-enabled operating model. In this pivotal role, the Associate Director will serve as the senior governance and relationship lead and is the accountable owner of Procurement Operations service delivery across PR-to-PO processing, Procurement Service Desk, and Vendor Master Data Management for outsourced procurement operations, ensuring the BPO partner delivers against contractual commitments, service targets, and strategic procurement objectives. The ideal candidate is a dynamic leader with deep expertise in end-to-end Procure-to-Pay processes, BPO governance, and continuous improvement. The ability to...

The Alliance Management Executive Director will lead the Alliance Management team in supporting the effective execution of global partnering at Vertex. All alliance managers will report to the Alliance Management Executive Director, who will be responsible for ensuring a consistent Alliance Management user experience across the company and helping to resolve issues across all alliances. In addition, the Alliance Management Executive Director will be a spokesperson for the function within Vertex and be responsible for keeping key stakeholders and senior leaders updated on collaboration status and engaging them in issue resolution and relationship management as appropriate. The Alliance Management Executive...

Company Overview Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases. Guided by a commitment to patients, scientific excellence, and operational integrity, Vertex brings together deep expertise, collaboration, and innovation to solve some of the most complex challenges in healthcare. Role Summary Vertex is seeking a Manager, TPRM Workflow & Risk Orchestration to join the Global Sourcing & Procurement organization within the Source-to-Pay (S2P) Center of Excellence . This role is responsible for designing and embedding third-party risk management (TPRM) into the end-to-end S2P lifecycle through workflow orchestration, lifecycle...

We are seeking an experienced and detail-oriented Senior Manager to support Procurement Operations and Vendor Management within Vertex's BPO-enabled operating model. Reporting to the Associate Director, the Senior Manager will play a critical role in overseeing BPO-delivered activities, monitoring performance against SLAs, enforcing procurement policy compliance, and driving continuous improvement across outsourced procurement workflows. This role requires a strong operator with excellent analytical and communication skills, and the ability to collaborate effectively with business stakeholders, Finance, Internal Controls, Category Management, and the external BPO partner. This role also supports operational execution across Procurement Req-to-PO, Service Desk and Vendor Master Data...

The Regulatory Strategy Associate Director will be responsible for overseeing the development of regional or global regulatory strategy for development programs or marketed products. This role will serve as a global regulatory lead, or in some cases a regional regulatory lead, for development and/or commercial product(s) within the Vertex portfolio and contribute to the global regulatory strategy for the assigned program(s). This role requires advanced understanding of regulatory affairs frameworks in the US, Europe, or other international markets, drug development, and related concepts, and the ability to translate this knowledge into effective regulatory planning and strategy development. Key Duties and...

Company Overview Vertex

The Project Management Director serves as the operational backbone of the GCO Digitization Strategy Center of Excellence, responsible for orchestrating the end-to-end portfolio of transformation initiatives across 6 workstreams, 50+ participants, and 10+ functional team transformation roadmaps. This role combines program management, value realization, and executive reporting into a single, high-impact position. The Director partners with GCOLT, DTE, and GCO functional leaders to ensure transformation initiatives are delivered on time, cross-functional dependencies are managed, risks are proactively mitigated, and business value is measured and communicated to leadership. This role is critical to ensuring the COE can scale its impact while...

Company Overview Vertex is a global biotechnology company committed to scientific innovation and improving the lives of people with serious diseases. Through a strong focus on patients, collaboration, and operational excellence, Vertex brings together talented professionals to build scalable, compliant, and efficient business capabilities that support its mission. Role Summary Vertex is seeking a Specialist, Buying Channel Orchestration & Enablement to join the Global Sourcing & Procurement organization within the Source-to-Pay (S2P) Center of Excellence (COE) . The Specialist is responsible for supporting the business owner with the enabling, managing, and optimizing buying channels and intake orchestration across the S2P...

Principal Scientist, Biologics, Sterile Drug Product Commercialization As part of Our Company’s Manufacturing Division, the Sterile Drug Product Commercialization group provides the technical process leadership and laboratory capabilities for late stage and commercial drug product processes for biologics. It is the division’s leader in sterile product and process development, responsible for late-stage commercialization activities including process scale up, technology transfer to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The group is responsible for establishing the science, engineering and knowledge required for today’s innovative and accelerated commercialization of biologics and combination products....

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Company's Animal Health group in Millsboro, DE is a Bio-Technology Center of Excellence that performs vaccine production operations from...

Are you enthusiastic and driven to create and lead execution of combination product testing strategies for innovative combination products? Join our company’s Device Development & Technology (DD&T) Team, which focuses on the design, development, and commercialization of novel biologic/drug/vaccine-device combination products for safe and effective delivery to their intended sites of action. The DD&T Team oversees the development of the device constituent within our pipeline of combination products, spanning various therapeutic areas and routes of administration, including inhalation, implantation, and injection. The Associate Principal Scientist will provide end‑to‑end technical and project leadership for the definition, integration, and execution of comprehensive...

North American GMP Operations, Rahway, NJ We invite individuals who possess a deep passion for promoting lifesaving and life-enhancing products to join our dynamic team. Our team is highly dedicated and committed to offering exceptional scientific oversight, driving the success of our Company's extensive range of products from candidate selection to market authorization. At our company, we proudly continue to build upon a legacy of groundbreaking innovation while steadfastly upholding the highest standards of ethics and integrity. With a workforce representing a multitude of languages and cultures, we stand unified in our collective mission to deliver revolutionary medicines and products...

In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Responsibilities This position supports the strategic design, development, and delivery of efficient, flexible, and modular analysis and reporting and submission standards and tools that can be used for drug and/or vaccine projects across all therapeutic areas. Adheres to standard operating procedures...

The Director of Customer Care is a key position in our company transforming our Customer Care organization. This role is responsible for elevating customer experience by evaluating and evolving our customer care model, which has been scaled alongside business growth and acquisitions. The incumbent will ensure internal and external customer journeys are seamless—enabled through a single point of entry and a customer-centric team delivering personalized, high-value interactions aligned to customer attributes. This leader will ensure that people, processes, systems, and third-party resources are harmonized and simplified to deliver end-to-end transparency, aligned KPIs, and consistently high customer satisfaction. In parallel, the...

The Discovery Pharmaceutical Sciences (DPS) group based in South San Francisco, CA is seeking a Principal Scientist with expertise in biologics formulation development and candidate selection. DPS is a multi-disciplinary research group that provides drug delivery, pre-formulation and formulation support for biologics and small molecules at the development and drug discovery interface. Our team is responsible for the characterization of pre-clinical drug candidates' physicochemical properties. We aim to work with partner groups to select candidates with optimal development properties while balancing all other key therapeutic properties. Our research also covers identification of preclinical formulations for pharmacology and toxicology studies and...

Senior Specialist, New Product Introductions Our ability to excel depends on the integrity, knowledge, imagination, skill, and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Direct Materials Procurement- New Product Introduction is responsible for the development and implementation of all supplier management strategies and initiatives, improving supply chain resiliency, and driving improvements in cost, supplier performance and working capital, in support...

Senior Empower Technical Lead Join us and be part of our dedicated team that provides support for our Global Manufacturing Laboratories to improve efficiency and compliance while improving our CDS Platform stability and useability. This opportunity will provide exposure to our Global CDS architecture and the multiple teams that provide support, which include file servers, databases and LACEs. Responsibilities Coordination of development resources and activities across DEV, UAT, and PRD environments. Serve as the primary technical authority for Empower configuration, integration, and validation in the manufacturing space. Configure and maintain LACE hardware and images. Develop and Maintain Interfaces to GLIMS,...

Our Scientists are our Inventors. We deliver robust scientific data and interpretation that drives the commercialization of breakthrough therapeutics using innovative thinking, state-of-the-art facilities and modern equipment. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing your career. The Analytical Enabling Capabilities organization in Rahway, NJ is seeking an experienced and highly motivated scientist with strong technical...

About DRACOE DRACOE (Decommission, Retire and Archive Center of Excellence) delivers secure, compliant, enterprise-scale data retirement and archive services across the company. We enable confident data retention, reduce infrastructure and application support costs, and remove security risk — all while improving data discoverability and usability. The Opportunity We’re building a best-in-class Live Archiving product to help our enterprise safely move petabytes of inactive or infrequently accessed data to cost-effective, searchable, and regulatory-compliant storage tiers — without disrupting user workflows. As Live Archiving Product Manager you will own product strategy and roadmap, influence technical design decisions across cloud and on-prem platforms,...

Scientist, Analytical R&D (Microbiologist) - Onsite The Analytical Research and Development Microbiology group has an opening for a Scientist - Microbiologist. Join us and experience our culture first-hand one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Scientist, you will be a critical part of the Analytical Research and Development Microbiology team with responsibilities including leading the rapidly growing pipeline via collaboration...

The Analytical Research and Development Microbiology group has an opening for a Scientist - Microbiologist. Join us and experience our culture first-hand one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Scientist, you will be a critical part of the Analytical Research and Development Microbiology team with responsibilities including leading the rapidly growing pipeline via collaboration with stakeholders to deliver on critical data...

The Customer Team Leader (CTL) plays a critical role in establishing our company customer- focused initiative. This is a field-based sales management position that is responsible for the North Central district, which includes and may not be limited to Nebraska, Iowa, Wisconsin, Minnesota, North Dakota and South Dakota. Key Responsibilities Lead and manage a team of Customer Representatives to deliver strong sales performance by accurately identifying and addressing customer needs. Provide coaching and guidance to Customer Representatives to enhance their skills and effectiveness. Oversee training programs and manage all people-related processes for the customer team, ensuring continuous development and optimal...

Brief Description of Position The Associate Director Quality Systems & Compliance within Device Quality & Regulatory will support our company's Manufacturing Division QMS Topic 3.3 – MDCP Design Controls and lead continuous improvement initiatives that support every aspect of our business processes, systems, and data. The Associate Director will collaborate with cross-functional teams to identify opportunities for improvement, address internal/external audit observations and tackle challenges, balancing effective operations with transformative initiatives. The Associate Director will work with the manufacturing division's Topic 3.3 Owner and Business Owner and has responsibility for oversight and lifecycle management of procedures related to this specific...

The Pharmaceutical Analytical Sciences group has an opening for a second shift Specialist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Specialist, you will be part of a team in charge of managing, coordinating, and facilitating analytical support for the Rahway...

Senior Scientist, Cell Culture Sciences, Biologics Drug Substance Commercialization Level R3 Location Rahway, NJ (primary) Join Our Team as a Biologics Cell Culture Senior Scientist! Are you ready to take your career to the next level? We are seeking a strategic and technical scientist with expertise in cell culture development & commercialization to spearhead our ever growing and dynamic late-stage biologics pipeline within the expansive Biologics S&T portfolio. Why You'll Love This Role As a Sr. Scientist in Biologics Cell Culture Commercialization, you’ll be at the forefront of scientific advancement, providing strategic and tactical technical direction through cross-functional partnerships with...

Our Company has an exciting and growing CV, Resp, Metabolic and Neuro pipeline, reinforcing our position as a sustainable innovation engine for the coming decade. Our Global Market Access (GMAx) organization is driven by a passion to save and improve lives through ensuring sustainable access to our medicines and vaccines at a price reflective of their value. We work collaboratively across the enterprise, and with regional and local market teams, to deliver the development and implementation of integrated access strategies, excellence in pricing strategy and execution, and shaping of the external access landscape. We drive sustainable patient access through innovation...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety...

We partner with the business to ensure we maintain our company’s values and high ethical standards, to comply with the law, protect our people and enhance our reputation. We strive to foster an inspiring and supportive environment. The successful candidate will join the Human Health Ethics and Compliance team, helping to advance the goal of the Ethics and Compliance Organization (ECO) to be a “partner in doing the right thing – all the time.” The Commercial Compliance Officer (CCO) will join the Commercial Compliance Team and will be responsible for compliance support for one or more functions within the Human...

Our Company’s Oncology organization is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of dauntless, forward-thinking individuals achieves this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic procedures, and collaborating with governments and payers to ensure that people who need medicines have access to them. At our company, our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. As we continue to grow and define the Oncology market of the future, we are...

The Senior Specialist, Promotional Review Training, plays a critical role in enabling US Market operational excellence by designing, delivering, and evolving training programs that support the end-to-end promotional review process. This individual serves as a subject matter expert across promotional processes, systems, and standards, ensuring Job Owners and agency partners are equipped to navigate our company's complex regulatory environments effectively. This role requires a growth mindset and the ability to continuously assess training needs, identify opportunities for improvement, and implement scalable, learner-centered solutions. The ideal candidate thrives in a fast-paced environment, collaborates across cross-functional teams, and ensures training programs align...

Senior Principal Scientist (Senior Medical Director) Translational Medicine, Immunology Translational Medicine in our Research & Development Division is responsible for planning and managing an important inflection point in the drug development process, working closely with scientific, regulatory, statistical, and modeling colleagues across the organization to translate the benchtop science of preclinical discovery into compounds ready for assessment in large clinical populations. We are seeking a highly qualified physician-scientist with a proven track record in both the pharmaceutical industry and independent academic research for a position in our group. Please note that our Senior Principal Scientist title is also equivalent to...

Position Overview Under the direction of the applicable management, the Clinical Data Manager (CDM) is responsible for executing end to end data management activities pertaining to clinical trials, including but not limited to; data management tool and system development, validation and maintenance, data collection, data integrity review and reconciliation, query management, medical coding, and database lock preparation, in compliance with our Company's Standard Operating Procedures (SOPs) and ICH-GCP guidelines. Primary activities include, but are not limited to Participates in the development and change request implementation of data management tools and systems for the clinical trial data management activities under the...

Translational Medicine is responsible for early clinical development of novel therapeutics, working in close collaboration with Immunology Discovery Sciences and late-stage Immunology Clinical Research. We work with all therapeutic areas within our Research Division with the role focused on Immunology. Principal Scientist (Medical Director level or known internally as Clinical Directors) must have a strong background in basic and/or clinical translational research and a desire to work collaboratively across different therapeutic areas Translational Medicine is specifically responsible for Leadership of the early clinical development strategy for novel therapy programs from Preclinical Candidate approval through Clinical Pharmacology testing (Phase 1),...

Our Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards. The Distinguished Scientist (Executive Director) and Product Development Team (PDT) Lead, Oncology Global Clinical Development, has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs in the Oncology Clinical Research group and in the field of Thoracic Oncology. The Executive Director, PDT Lead will manage the entire cycle...

Join Our Company’s Manufacturing Division as a Director/ Principal Scientist, Biologics Drug Substance Commercialization (BDSC). This senior leadership role is responsible for driving late-stage and commercial biologics programs, focusing on upstream cell culture and commercialization . The position oversees a team of scientists, leads high-impact process development, and manages technology transfer and validation activities to support licensure and commercial manufacturing. Key responsibilities include providing technical leadership in process characterization, ensuring regulatory compliance, collaborating across cross-functional teams, and fostering innovation and operational excellence. Candidates should possess deep expertise in upstream biologics processing, proven experience in commercialization and scale-up, and strong leadership...

The Cardiometabolic Disease (CMD) department at our company's Research Labs South San Francisco is seeking a highly innovative and technically rigorous Scientist/Senior Scientist with deep expertise in preclinical in vivo models, particularly in cardiovascular and renal disease biology. This role is centered on hands-on ownership of complex rodent in vivo models and advanced physiological phenotyping to enable mechanistic discovery and target validation. The successful candidate will design, execute, and interpret sophisticated in vivo studies, often involving surgery, invasive measurements, and longitudinal functional readouts, and directly influence target selection and early translational strategy for cardio-renal programs. The position requires a scientist...

Oncology Customer Team Leader (District Sales Manager) – Atlanta, GA Grow and accelerate your career with our Oncology Sales organization and join a team that’s driven to make an impact on cancer patients. We take a customer-centric approach by leveraging emerging digital technologies and data analytics to better understand our patients' needs. Developing your career with us will allow you to join a group of diverse professionals, driven by purpose and determined to help save and improve lives. Help us continue to grow and define the oncology market of today and tomorrow with a driven, customer-focused, and collaborative team. As...

The Senior Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. Specifically, The Senior Director May Be Responsible For Evaluating pre-clinical and translational work for the purpose of generating the early clinical development plan and Investigational New Drug applications. Providing clinical development support of business development assessments of...

Senior Scientist, Cell Culture Sciences, Biologics Drug Substance Commercialization Level R3 Location Rahway, NJ Join Our Team as a Biologics Cell Culture Senior Scientist! Are you ready to take your career to the next level? We are seeking a strategic and technical scientist with expertise in cell culture development & commercialization to spearhead our ever growing and dynamic late-stage biologics pipeline within the expansive Biologics S&T portfolio. Why You'll Love This Role As a Sr. Scientist in Biologics Cell Culture Commercialization, you’ll be at the forefront of scientific advancement, providing strategic and tactical technical direction through cross-functional partnerships with key...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do Summary of the job Our Senior Territory Representative interacts face to face with our customers, understand their needs and consult...

In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Responsibilities This position supports the design, development, and delivery of efficient, flexible, and modular analysis and reporting and submission standards that can be used for drug and/or vaccine projects across all therapeutic areas. Adheres to standard operating procedures and guidelines established...

Reporting to the Associate Director of PTO Engineering, the Senior Process/Project Engineer is responsible for providing technical support to Manufacturing Division–Wilson packaging operations (including oral solid dose and bottle packaging lines) as well as medical device assembly lines. This role involves planning, designing, and implementing technical projects while serving as a subject matter expert (SME) for assigned packaging lines and associated processes. The position requires strong technical expertise, project management capability, and knowledge of company standards, procedures, and practices. Key Responsibilities Specify, procure, install, and qualify new packaging and medical device assembly equipment. Provide ongoing technical support, performance monitoring, and...

As a Cardiovascular Disease Specialist, you will drive meaningful patient impact by leveraging our scientific expertise and serving as the primary contact for customers within your assigned territory. As a key member of the local Customer Team, you will collaborate closely with Account Executives, Integrated Delivery Systems leaders, and other field colleagues to deliver seamless, patient-focused solutions. Territory Assignment This is a field-based sales role responsible for covering the Johnstown, Pennsylvania territory. Major areas of this territory include and may not be limited to Johnstown, McKeesport, and Bedford, Pennsylvania. Travel (%) depends on the needs of the territory and where...

We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in patients with Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease...

We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in patients with Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease...

We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in patients with Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease...

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans....

We are searching for the best talent for Neuroscience Sales Specialist to cover the territory of Salt Lake City North, UT. The Neuroscience Sr Sales Specialist will be responsible for promoting Spravato in their respective sales territory. The Neuroscience Sr Sales Specialist will be the territory business owner, responsible for using approved sales strategies and CAC-approved materials, implementing strategies and executing tactics to optimize appropriate product utilization and achieve sales goals. The Neuroscience Sr Sales Specialist must comply with all corporate policies, SOPs, and applicable federal and state healthcare laws. About Innovative Medicine Our expertise in Innovative Medicine is informed...