Jobs at Biogen
25,826 open positions
Biogen, a global biotechnology leader, pioneers treatments for neurodegenerative diseases using innovative mRNA and gene‑editing platforms. While rooted in pharma, the company heavily relies on data‑driven technology, offering roles in software, bioinformatics, and AI that power drug discovery and patient‑centric solutions.
Biogen’s tech hiring spans software engineers (front‑end, back‑end, full‑stack), data scientists, bioinformatics analysts, cloud architects, and cybersecurity specialists. Applicants can expect a structured interview process that includes coding challenges, system design questions, and domain‑specific problem solving tied to biological data.
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Sr. Manager, Product Development Quality
Company: Biogen
Location: Cambridge
Posted Oct 25, 2023
The role of a Quality Product Leader at Biogen involves managing quality aspects of product development and commercialization, collaborating with various teams, and ensuring adherence to GMP guidelines. The ideal candidate should have a STEM background, experience in pharmaceutical development, and strong cross-functional collaboration skills. Biogen values diversity and inclusion, offering a mission-driven work environment with opportunities for professional growth.
Senior Manager, Product Development Quality
Company: Biogen
Location: Raleigh-Durham, NC
Posted Oct 25, 2023
This role, a Quality Product Leader, is responsible for managing the Quality aspects of Product Development and Commercialization. The ideal candidate should have Biologics technical expertise, deep knowledge of GMP guidelines, and strong communication skills. The role involves approving controlled documents, protocols, and reports, and acting as the final approver for regulatory submissions. The position requires a Bachelor's or Master's or PhD in STEM with relevant experience in Quality and pharmaceutical development. Cross-functional collaboration, project management skills, and the ability to mentor colleagues are essential. Biogen values diversity and inclusion, and the role offers the opportunity to work on therapies for neurological and rare diseases.
Associate III, Quality Assurance
Company: Biogen
Location: Raleigh-Durham, NC
Posted Sep 20, 2023
Together, we pioneer. Read on to learn more about our DE&I efforts.All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Together, we thrive.At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. Biogen is an E-Verify Employer in the United States. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients’ lives and on changing the course of medicine. Additionally, you have excellent communication/collaboration skills, logical thinking, and can work across all levels of the organization.QualificationsBachelor’s degree preferably in a field of science or biotechnology.A minimum of 2 years relevant technical experience in quality oversight of a biotech or pharmaceutical manufacturing operation.General understanding of relevant FDA/EMA regulations and compliance.Strong organizational skills.Must be able to deal with ambiguity.General foundation of Quality concepts; able to practice and implement them.Ability to develop innovative/creative solutions to issues of moderate complexity.Detail oriented aptitude.Excellent oral and written communication skills.Preferred SkillsExperience in DS manufacturing operation.Additional years of experience in quality.Additional InformationWhy Biogen?Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. Aide in implementation of Quality Systems/System Improvements with some guidance, moderate technical problem solving (tools or enterprise systems) within function and across multiple functional areas.Assist Quality Assurance Management in additional responsibilities related to the day-to-day implementation of the Quality Management Systems required to maintain cGMP compliance, and ensure the safety, efficacy and purity of the products manufactured by Biogen.Support and/or assist in GxP quality systems-related training. The QA Associate III will also support leadership for activities related to interviewing and training of employees, as well as compliance with training policies.What You’ll Do Review and approve batch related documentation (cGMP procedures, Master Production Records, Solution Lot records) to support drug substance disposition.Execute activities including intermediate technical writing, intermediate investigation support (root cause analysis/impact assessment), project representation (moderate complexity).Support resolution of both technical and compliance issues/gaps of moderate complexity.