Today's Pharma & Biotech Jobs

We are seeking a highly motivated and scientifically driven Senior Scientist- Cancer immunology/immunotherapy with deep expertise in cancer immunology and immunotherapy to join our Oncology research team. The successful candidate will bring extensive experience in T cell biology, neoantigen discovery, immunopeptidomics, and immune function assessment in both in vitro and in vivo systems, with a particular interest in cancer vaccine development. You will independently design and execute complex research studies, troubleshoot and optimize experimental approaches, and generate high-quality scientific data that advances our understanding of anti-tumor immune responses and enables the development of novel immunotherapeutic strategies. As a Senior Scientist,...

Available locations Gaithersburg, MD Boston, MA South San Francisco, CA Santa Monica, CA Introduction to role Are you ready to set the global regulatory vision for pioneering cell therapies and turn breakthrough science into real options for patients? This role leads high-impact programs across cancer, immune-mediated and rare diseases, guiding them from current stage through licensure with clear, competitive pathways to approval and labeling. You will shape strategy for complex, visible programs, bringing clarity, pace and rigor that accelerate access for patients. You will report to the Executive Director, Cell Therapy Regulatory Affairs and act as a franchise global regulatory...

Job Title Director, Regulatory Affairs Strategy - Cell Therapy Available locations Gaithersburg, MD Boston, MA South San Francisco, CA Santa Monica, CA Introduction to role Are you ready to steer global regulatory strategy for cell therapies that redefine standards of care for patients? In this Director role, you will shape the regulatory path for programs that span oncology, immune-mediated and rare diseases—translating breakthrough science into timely approvals and competitive labeling that make a tangible difference to patients and markets. You will join a high-performing, cross-functional environment where regulatory insight is central to program decision-making. Partnering with senior leaders and...

Johnson & Johnson is currently seeking a Supplier Development Engineer Co-op to join our Supplier Engineering Team located in Danvers . 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 profoundly impact health for humanity. Requirements Support standardization of manufacturing defect...

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 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 the burden...

POSITION SUMMARY You will lead a team of analytical scientists supporting the development of Pfizer's small molecule drug products from early development through commercialization. You will drive analytical strategy, portfolio delivery, scientific excellence, innovation, and talent development while collaborating across multidisciplinary CMC teams. KEY RESPONSIBILITIES Provide leadership and coaching to Analytical Scientists, fostering technical growth and high performance. Define and execute analytical development strategies supporting clinical and commercial milestones. Lead analytical project planning, resource management, budgeting, risk assessment, and delivery of CMC analytical activities. Partner with Drug Product Design, Supply Chain, Quality, Regulatory, Clinical, and Commercial teams to ensure successful...

SENIOR MANAGER, DRUG PRODUCT ANALYTICS POSITION SUMMARY You will lead a team of Analytical Scientists supporting Pfizer’s small-molecule portfolio from early development through commercialization. You will provide scientific and people leadership for analytical development, control strategy, and project delivery, working closely with Drug Product Development and Supply and other CMC functions. You will be accountable for defining phase-appropriate analytical strategies, translating scientific data into clear project recommendations, and ensuring robust analytical deliverables aligned with program timelines and regulatory expectations. You will also coach and develop scientists, strengthen technical capabilities, and identify opportunities to improve development speed, scientific quality, and operational...

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. Main responsibilities Serve as the primary functional expert for the enterprise GTN forecasting and planning platform across all Market Access workstreams, including GTN Channel Forecasting, Accrual & Reserve Analysis, and Pre-Deal and Post-Deal Analytics models, with deep knowledge of model mechanics, calculation logic, and data flows. Understand the data model design and architecture within Anaplan, including the structure of lists, modules, line items, and...

The Associate Director of Managed Care Operations is a key operational role responsible for supporting and advancing the operational, regulatory, and technological functions within Managed Care Operations. This position plays an important role in helping ensure the organization's compliance with federal programs, driving process improvements, and contributing to high-priority strategic initiatives that impact financial performance and operational efficiency. The Associate Director will serve as a lead contributor for the CMS Maximum Fair Price (MFP) initiative—a high-visibility federal program spanning design through execution—supporting the development of internal process architecture, helping define business requirements, and taking ownership of day-to-day operations post-launch. Additionally,...

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Responsible for testing of incoming raw materials, sampling, labeling tracking and shipping of samples. Performance of appearance for drug product....

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now...

We are in search of a Manager, Statistical Programming to join our team! Statistical Programming– Analysis Programming Statistical programmers work collaboratively with internal colleagues and external vendors to ensure the efficient, high-quality production of analysis datasets and statistical outputs for study reports and integrated summaries in support of Gilead’s regulatory, scientific and business objectives. Key Responsibilities Works collaboratively with Clinical Development staff to meet project deliverables and timelines for statistical data analysis and reporting. Generates or oversees the production of programming deliverables (e.g., tables, figures, listings) for study reports and integrated summaries. Ensures programming and corresponding documentation is completed in...

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now...

Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Gilead therapeutic areas. Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gilead’s products. You will manage a geographical region(s) of assigned clinical studies or multiple components of larger studies. You will typically manage Phase I studies or other smaller studies. You will define and incorporate study logistics and study plans to accomplish...

We anticipate the application window for this opening will close on - 24 Sep 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 This specialized Principal Manufacturing & Injection Molding...