$111,000 – $149,000
Listed on Biogen’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role leads data integrity and compliance initiatives across a pharmaceutical manufacturing site, ensuring adherence to FDA regulations and quality standards. It suits experienced quality professionals who thrive in regulated environments and can drive cross-functional improvements while managing complex compliance programs.
Our summary, not Biogen’s wording. The full posting is on their site.
What they ask for
Required
- Bachelor's degree in scientific, technical, or relevant discipline
- Minimum 6 years of Quality Assurance experience in pharmaceutical, biotech, or manufacturing
- Deep knowledge of data integrity principles and FDA 21 CFR Part 11 and cGMP regulations
- Experience with computerized systems and electronic records
- Experience in Quality Control environments
- Strong analytical, organizational, and communication skills
- Ability to manage multiple priorities and drive results
Nice to have
- Master's degree or MBA
- Experience leading data integrity programs in GMP-regulated environments
- Familiarity with Veeva, TrackWise, and Power BI
- Experience supporting regulatory inspections and audits
- Strong stakeholder management and cross-functional collaboration skills
- Demonstrated ability to drive continuous improvement in quality systems