Today's Pharma & Biotech Jobs

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. Our Cardiovascular and Metabolism team develops breakthrough treatments for diseases that burden hundreds of millions of people. Joining this team will bring your innovative talents to the forefront of preventing and managing life-threatening diseases. 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 Job Specification - Executive Administrator Reports to ...

Senior Associate Scientist – In Vivo Pharmacology Location Bothell, WA Organization Oncology Research Unit (ORU) – In Vivo Pharmacology Position Type Full‑time Career Level Senior Associate Scientist (Non‑PhD track) The Oncology Research Unit (ORU) is seeking a hands-on, execution focused Senior Associate Scientist to join the In Vivo Pharmacology group at the Bothell, WA site. This role is primarily responsible for the execution of in vivo experiments supporting preclinical oncology drug discovery programs, including antibody drug conjugates (ADCs) . The Senior Associate Scientist will perform in vivo efficacy, PK/PD, and mechanistic studies , along with in vitro aseptic mammalian...

The Technical Specialist’s primary responsibility is to provide basic husbandry, handling, restraint and health surveillance of laboratory animals in compliance with local regulatory requirements. This individual will also be responsible for maintaining inventory of animal supplies and providing basic technical assistance (i.e., restraint, injections, blood collections) in support of research studies. Perform all regulatory responsibilities in compliance with applicable regulatory standards. How You Will Achieve It Primary Duties Perform routine animal husbandry duties as directed. Observe and report status of animal health, food and water consumption, appearance, behavior. Provide support in basic veterinary medical treatment as prescribed by the veterinary...

ROLE SUMMARY As a Federal Government Contract Manager, you will be accountable for having a general working knowledge of the pharmaceutical and managed care industries and experience in Federal government contracts. You will be responsible for assisting in and preparing Federal contract offers based on complex data analysis, compliance with Federal contract regulations, identifying risks, and assisting in or developing strategic recommendations for presentation and approval to upper management. You will be responsible for your specific assigned accounts, the analytics and contract lifecycle management including payments. This role is oriented similar to project management-like way in that you will...

The Study Start Up Lead is responsible for providing leadership in the execution of operational strategy and management of start-up activities for all clinical trials, across all therapy areas. The role is the accountable person and single point of accountability for the study Start Up Metrics. This position works directly with Study Start Up Associate Director, LDL Managers, LDL, Global SSU Managers, CRO FSP (Functional Service Provider) CRA/CSA Managers in setting priorities and expectations for Study Start-Up. Key Responsibilities Accountable to lead timely Start Up, operational management, completion and delivery of all clinical studies across multiple therapeutic areas to agreed...

We anticipate the application window for this opening will close on - 3 Jun 2026 Position Support engineering function within new product development for large development lifecycle of complex electro-mechanical & electronic medical devices. Design test methods and statistical process control procedures for achieving required levels of product reliability. Compiles and analyzes performance reports and process control statistics & investigates and analyzes relevant variables potentially affecting product and processes. Responsible for Medical Device Risk and deliverables to include Risk Analysis, Design, Use and Process Failure Mode Effects Analysis (xFMEAs), and Risk Assessment. Author reliability studies and evaluations of engineering...

About the Role The Associate Director, Federal Government Affairs (FGA) will contribute to Takeda’s advocacy efforts and help execute strategies aligned with legislative and executive branch priorities. As a key internal expert on the external environment, th is role will provide strategic insights identify ing threats and opportunities related to commercial, clinical, and operational practices . T he Associate Director , Federal Government Affairs will collaborate with internal teams and external stakeholders to advance good policy and mitigate against harmful ones , ensuring alignment with Takeda’s business objectives . This individual will be responsible for building a variety of strong,...

About the Role The Ass ociate Director, Patient Advocacy and Strategic Partnerships shapes and executes patient advocacy strategies that align with therapeutic area priorities, policy and access objectives , and broader corporate goals. This role leads the planning and delivery of patient advocacy programs and engagements ensuring high-quality, compliant execution and measurable impact. The Ass ociate Director builds and stewards thoughtful, ethical, and compliant partnerships with patient advocacy organizations and coalitions, representing Takeda in external forums as needed to advance shared advocacy, policy, and access objectives . As a cross-functional collaborator across US BU, I nternational BU, and S trategy...

About the Role The Therapeutic Policy and Advocac y Lead , GI (Associate Director) executes patient advocacy strategies that advance shared priorities for the US Business Unit (USBU) , Strategy and Portfolio Development (SPD), and the International Business Unit (IBU) for an assigned therapeutic portfolio of in-line and pipeline medicines. The role drive s strategic engagement with patient group partners across the development and commercialization continuum, including addressing access policy and barriers to optimal care. This role also ensure s patient s’ and caregivers ’ perspective s are included in company discussions and decision making . How You Will Contribute...

About the Role The Sr Manager, Public Affairs and Operations, supports U.S. Public Affairs (USPA) by managing compliance, communications, stakeholder engagement, and project execution across internal and external initiatives. This role serves as a key liaison across teams, ensuring effective coordination, timely delivery of communications, and alignment with organizational priorities. How You Will Contribute Manage state and federal lobbying compliance requirements, including tracking, reporting, and coordination with internal and external stakeholders. Lead USPA internal communications initiatives, including regular updates ( e.g . 5 Things to Know in Massachusetts) and other targeted communications. C oordinate and assist with the development of...

About the Role The Associate Director, State Government and External Affairs (SGEA) is responsible for maintaining and enhancing positive relations with external and internal audiences, including elected officials , stakeholders , and government entities. This role focuses on influencing public opinion, government policy, and legislative direction to improve the organization's regulatory and economic environments. The position is based in Minnesota which will be the primary state of focus. How You Will Contribute Develop and implement communication strategies to influence public opinion and government policy Establish and maintain relationships with key stakeholders, including government officials and community leaders Lead advocacy efforts...

About the Role The Senior Manager, Communities of Practice and Operations facilitates collaboration with public affairs colleagues on critical policy topics and oversees the organization of related projects to ensure alignment and effectiveness. This position also plays a role in managing and executing tasks associated with Takeda’s engagement with trade associations and other external groups . This role reports directly to the Director, Public Affairs and Operations, providing strategic support on a variety of U.S. Public Affairs initiatives. How You Will Contribute Facilitate public affairs communities of practice for Takeda colleagues, encompassing international and U.S. public affairs, public policy, community...

The Senior Informatics Sales Specialist will use their strong genomics and Informatics technical knowledge and expertise to identify and close Informatics opportunities. This involves selling to prospective customers and Illumina colleagues on Next Generation Sequencing and Genomic data analysis pipelines, applications and products primarily for use in research and academia. They will act as an influencer and expert resource for customers and others to ensure success while enabling sales growth through strategic activities and creative problem solving. The Informatics Sales Specialist should be viewed as a “go to” subject matter expert for all things Informatics, with primary focus on Illumina’s...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Senior Director, Thought Leader Liaison - Northeast Immunology –...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. DES MOINES IA GI1_166823 Company overview For more than a century,...

Expected Areas of Competence Develop and lead Global and US Regulatory activities for a Development Team (s), leveraging primarily external resources for operation activities, and internal resources for strategic and HA engagement. Collaborate and influence internal BMS expertise and external regulatory resources to assure regulatory issues are addressed in development plans Provide leadership to resolve critical regulatory project issues, bring the appropriate regulatory experts together as needed Establish sound regulatory advice/position on key development issues, and communicate same to DTL and other team stakeholders Develop registration strategy for a product, and translate that into operational...

Why Genentech We’re passionate about delivering on Our Promise to improve the lives of patients and create healthier communities for all. We foster a culture of inclusivity, integrity and creativity while boldly pursuing answers to the world’s most complex health challenges and transforming society. About this Marketing Position The Marketing organization influences decisions by establishing and communicating our full product value proposition across the full value chain, from payers, to health systems, to prescribers, to patients. Marketers are masterful storytellers - accountable to inform positioning using an insight-driven marketing strategy, deliver simple compelling customer-led content creation, and design outstanding integrated...

Facilities Engineer This position works out of our Barceloneta location in the Vascular division. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease. The Facilities Engineer plans, designs, and supervises the construction of new, or existing, facilities in support of Company goals by utilizing available resources in the most efficient and effective manner possible while complying with time and budget constraints. Projects range from small to mid-sized and have moderate impact on overall company goals. Performs investigations and implements corrective actions in support of Exception process for both moderate and major CAPAs affecting...

Production Supervisor This position works out of our Arecibo location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Shift second, Monday to Friday As the Production Supervisor, you will provide team leadership in the day-to-day activities for an assigned production area or work group. Responsible for the development and implementation of production process excellence activities; identify and execute continuous improvement opportunities in production processes, plans tasks and solutions. Reports to functional and/or organization...

We’re empowering smarter medical and economic decision-making to help transform how people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott’s diagnostics instruments, providing lab results for millions of people. The Enterprise Account Manager works remotely within the Core Diagnostics Division and will be responsible for the Great Lakes Region (ideal candidate will be located in Ohio)This position sells the entire Abbott Core Laboratory Diagnostics Division product line to large, complex strategic named accounts and strategic named prospect accounts. This role will focus on the strategic customer relationship, retention,...

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...

The Executive Director, Research & Clinical Development Quality Assurance provides senior leadership and strategic oversight for Quality Assurance activities supporting nonclinical (GLP/GCLP) and clinical development (GCP) programs, as part of Sarepta’s Corporate Quality organization. This role is accountable for the effective execution of Quality Assurance responsibilities, including auditing, compliance oversight, and inspection readiness across critical phases of development, while maintaining appropriate independence from study execution teams. The Executive Director ensures Quality systems, processes, and controls are designed, implemented, and maintained in compliance with GLP, GCP, GCLP, and applicable regulatory requirements (FDA, OECD, ICH). Operating within the Corporate Quality Organization, this...

Purpose The HR Manager is a strategic and trusted partner to the business, helping to shape our culture, support our business strategies and deliver the talent necessary to make a remarkable impact on AbbVie and patients around the world. This role is responsible for leveraging best-in-class HR practices to continually create, deliver, and support programs that establish AbbVie as an employer of choice while empowering all employees at all levels of the organization. This role will serve as a strategic HR partner to multiple VPs in our AbbVie Quality organization in the Operations function, to develop and implement people strategies...

This role is based onsite at AbbVie's North Chicago, IL headquarters Tuesday-Thursday on a weekly basis. Physician’s Development Program Overview AbbVie’s Physician’s Development Program (PDP) is a robust, two-year rotational program specifically targeting Medical Doctor (M.D.) specialist talent (graduating fellows). Those who have completed their M.D. program will also be considered. The goal of the program is to develop and support high-potential specialist physician talent in transitioning to a successful career within R&D at AbbVie. To that end, participants will engage in thoughtful, impactful rotational assignments within core R&D sub-functions, including Clinical Pharmacology & Pharmacometrics, Pharmacovigilance, Medical Affairs, Regulatory Affairs,...

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. The Medical Science Liaison (MSL) is field-facing role whose main objectives are to Be the trusted scientific partner to key external experts by conducting timely, appropriate and frequent scientific exchanges to enhance the understanding of the scientific and medical value of our products. Execute on stakeholder engagement plans to gather data, develop and share medical insights that contribute to enhancement of Sanofi’s key medical...

Associate Director, Regional Con ference Lead is responsible for leading the strategy and execution of Vertex’s U.S. Kidney Business Unit commercial representation at regional conferences as part of the Market Development team . The Associate Director has responsibility for plan ning and delivery across approximately 4 0+ regional -level conferences annually and reports into the Senior Director, Market Development with direction fr o m t h e Director , Congress, Ad Board, and Strategic Council Lead, US Kidney and Director, Customer Engagement Liaison Lead . Key Duties and Responsibilities Lead s regional conference p rogram within the U.S. Commercial Kidney...

Pharmaceutical Sales Specialist - Primary Care R & I - Las Vegas, NV 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...

The Manager, Quality Assurance is responsible for supporting and maintaining compliance with the Quality Management System (QMS) and applicable regulatory requirements. This role ensures that manufacturing, testing, and release activities for cell therapy products are conducted in accordance with cGMP standards and company procedures. The position provides day-to-day oversight of Quality Assurance activities, supports cross-functional teams, and contributes to risk assessment and continuous improvement initiatives. This role supports operations across the Santa Monica, CA and Tarzana, CA sites and reports to the Director of Quality Site Head. Key Responsibilities Support management of the Quality Assurance team, including training, scheduling, and...

The Director, Clinical Marketing – Neurovascular is responsible for leading the development and execution of clinical marketing strategies that support the adoption and growth of the company’s neurovascular portfolio. This role serves as the critical link between clinical evidence, physician education, and commercial execution by translating clinical data, treatment insights, and real-world outcomes into clear, compelling value propositions. The Director will work closely with Medical Affairs, Clinical Affairs, Sales Leadership, R&D, and Professional Education to ensure that clinical differentiation is clearly communicated to physicians, hospital systems, and other key stakeholders. This role plays a critical part in enabling the commercial...

Bring your talents to an industry leader in medical technology and healthcare solutions – we’re a market leader and growing every day. You can be proud to part of technologies that are rooted in our long history of mission-driven innovation. You will be empowered to shape your own career. We support your growth with the training, mentorship, and guidance you need to own your future success. Together, we can transform healthcare. Join us for a career in IT that changes lives. The Senior Software Engineer acts as a software architect for the AC&M R&D organization and the development lead for...

The Medical Writer (MW) works with team members to write the content of clinical documents that may include CSRs, protocols, ICFs, narratives and IBs in a variety of therapeutic areas. The MW may serve as lead for a compound and is expected to resolve issues and escalate problems, as necessary. As a Medical Writer, a typical day may include Works with team members and with MW lead oversight to create the content of clinical documents that may include CSRs, protocols, ICFs, narratives and IBs in a variety of therapeutic areas. The MW may serve as lead for a compound and...

Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry leaders ensuring the scientific value of our products is understood. We connect, communicate and train internal employees to ensure a thorough understanding of the science behind the medicine and review further unmet medical needs to support collaboration to further differentiate our portfolio. The Genitourinary Oncology Regional Medical Scientific Director, RMSD, is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. Scientific exchange does not include promotional...

Johnson & Johnson is recruiting a Analyst to support Procurement . The primary location for this role is Raritan, NJ, with alternatives at New Brunswick, NJ. Titusville, NJ, and Spring House, PA. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and...

E&PS is recruiting for a Sr Manager Medtech Project Controls, to be located in New Brunswick, NJ. 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 The Senior Manager, Project Controls is accountable for ensuring compliance with J&J Worldwide Procedures and the implementation of scalable E&PS Project Controls tools, guidelines and industry best practices throughout the lifecycle of the project. This candidate will require a strong background in estimating, cost control,...

#LI-Hybrid Join Novartis and have the opportunity to lead and scale a global, in house web operations capability supporting all US promoted brands, delivering compliant, high quality digital experiences while driving measurable gains in efficiency, quality, and cost. As Associate Director, Web Operations, you will own end to end production, establish fit for purpose standards and processes, and serve as a key partner across Integrated Marketing Operations, agency partners, and cross functional stakeholders. Leading globally distributed teams, you will continuously elevate web operations to enable greater agility, speed, and execution excellence—helping the organization operate more strategically in service of improving...