Today's Pharma & Biotech Jobs

Purpose The Pharmaceutical Operator II is responsible to properly execute the Manufacturing processes, equipment Operation and corresponding SAP transactions. The execution should be always according the Manufacturing instructions following the Good Manufacturing Practices (cGMP) and Safety (OSHA) regulations. Responsibilities Responsible for Cleaning, Set Up and Operation of all equipment related to Manufacturing process. Responsible for receipt, verification and usage of raw materials to be used within the process Responsible to follow manufacturing order instructions, basic operating procedures process related and procedures related to safety and Good Manufacturing Practices (cGMP). Responsible for quality, productivity and process efficiencies under execution Responsible for...

The Senior Clinical Trial Associate, Clinical Operations is an advanced professional who supports in the planning, execution, and management of clinical trials. The Opportunity to Make a Difference Coordinates and tracks the distribution and subsequent retrieval of clinical documents, including but not limited to protocols, protocol amendments, IBs, ICF’s, monitoring visit reports, etc. Supports maintenance of inspection-ready Trial Master File (TMF) according to ICH-GCP and company SOPs Performs quality checks on the study TMF with oversight of study Clinical Operations Lead (COL) Assists in the preparation of study related documents, i.e., ICF, clinical trial tools and templates, etc. Coordinates and...

 Position Overview Summary The Senior Manager, R&D Training System and Operations co-manages Sarepta’s global GxP Training Program. This is a remote role requiring occasional travel to Massachusetts and Ohio sites a few times a year for collaboration and regulatory inspection support. As a working leader, this role balances hands-on operational execution with strategic program management. Key responsibilities include maintaining a compliant global GxP training program, managing the validated Veeva Training Vault LMS, and ensuring the accuracy and compliance of all governing SOPs. The position directly ensures that global personnel are properly qualified to perform their roles across the following...

The Director, Patient Focused Drug Development and Innovation at Sarepta Therapeutics is a pivotal role dedicated to building patient focused drug development frameworks while advancing Sarepta’s patient-centric approach across multiple disease areas. Reporting directly to the Senior Director, Patient Affairs Strategy and Operations, the Director, Patient Focused Drug Development and Innovation will design and lead strategic collaborations to ensure patient focused drug development across the pipeline and embed the patient voice into R&D decision-making. This role integrates the perspectives of patients and caregivers into the strategic and operational framework of the organization, spanning research and development to develop innovative solutions...

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...

Provide leadership and guidance as the lead biostatistician on one or more project team(s) and cross-functional teams, accountable for all statistical aspects of project(s). Act as statistical consultant within company. 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. About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and...

The Scientific Logistics and Assay Life Cycle Management Team Lead is responsible for optimizing operational, scientific, and safety aspects across GCI, while efficiently allocating staff resources to meet business priorities. The role also drives documentation and continuous improvement and serves as the main point of contact for digital, FELS, BIOS, and lab initiatives. This role involves collaborating with GCI platform heads and Global Immunology leads to identify operational needs, address bottlenecks, and implement best practices. The successful candidate will ensure operational efficiency and foster a culture of continuous improvement within GCI. This position reports to the Head of Global Clinical...

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...

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 4 to 6 hours per day, 3 or more days per week —designed to fit your life. We will confirm availability, along with shift days and times, early in the interview process. Team members will be informed in advance of any schedule changes. Our patients depend on the plasma we collect, so reliability during scheduled hours is greatly valued. At the same time, these part-time roles...

$2,000 Sign-On Bonus Eligible 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...

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...

This role requires that all individuals on the team hold one of the following current/active certifications California Certified Phlebotomy Technician 1 License (CPT1), a California Certified Phlebotomy Technician 2 License (CPT2), a California Clinical Laboratory Scientist License (CLS), or a California Medical Laboratory Technician License (MLT). 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...

$2,500 Sign on Bonus Eligible 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...

Regional Sales Director- Immunology Business Introduction GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centered on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems. Our diverse portfolio consists of vaccines, specialty medicines, and general medicines. Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and...

We anticipate the application window for this opening will close on - 31 Jul 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life In the role as Product Owner, you...

Overview Johnson & Johnson MedTech is focused on shaping the future of digital surgery and expanding its robotics and digital solutions offerings across the entire portfolio, with multi-specialty, end-to-end solutions in endoluminal intervention, general surgery and a comprehensive digital portfolio. This includes the Polyphonic® platform, a first-of-its-kind digital platform that advances patient empowerment, surgical performance, operating room (OR) collaboration and operational efficiency by synchronizing devices, data and AI driven insights in one place to simplify access, build confidence and unify a non-linear care experience. We are recruiting for a Principal AI Lead within the Polyphonic® Applied AI and ML team...

Job Title Territory Manager, CardioMEMS - Long Island, NY Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year An excellent retirement savings plan with high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit...

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. The Packaging Technician position is available at our Animal Health facility in De Soto, Kansas, located near Kansas City metropolitan...

We anticipate the application window for this opening will close on - 3 Aug 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life At Medtronic, we bring bold ideas forward...

Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. May assist with method transfer, documentation, deviations, investigations, and continuous improvement efforts. Responsibilities Perform routine testing of in-process, final product, and stability samples. Perform testing for method transfer/validation/verification. Perform data verification, data review and review of GMP documentation for general methods. May perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts. Train analysts on general job duties. Perform other tasks as assigned. Reporting Relationship This position will report to QC management. Qualifications Specific Knowledge, Skills, Abilities Ability to...

Subject matter expert supporting method transfer/validation and routine testing of in-process, final product, and stability samples. Perform data review/verification, complex troubleshooting, and method training. Own project, document revisions, deviations/investigations/CAPA, and continuous improvement efforts Key Responsibilities Subject matter expert supporting method transfer/verification/ validation and routine testing of in-process, final product, and stability samples. Perform review of testing data (e.g., data packets, final lot file, COA review). Anticipate and perform complex troubleshooting and problem solving independently. Perform data verification, data review and review of GMP documentation for multiple methods (general and complex) and/or products. Own project, CAPA...

Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. May assist with method transfer, documentation, deviations, investigations, and continuous improvement efforts. The shift for this position is B2 (2pm-12am, Wednesday-Saturday). Duties/Responsibilities Perform routine testing of in-process, final product, and stability samples. Perform testing for method transfer/validation/verification. Perform data verification, data review and review of GMP documentation for general methods. May perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts. Train analysts on general job duties. Perform other tasks as assigned. Reporting Relationship...