$178,000 – $245,000
Listed on Biogen’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
A director-level position leading validation, transfer, and regulatory filing efforts for biologics and analytical instruments across clinical and commercial stages. Suited for a scientific leader with pharmaceutical regulatory experience who can drive cross-functional alignment and modernize testing strategies.
Our summary, not Biogen’s wording. The full posting is on their site.
Skills this role names
Log in to see which of these are already on your profile.
What they ask for
Required
- Bachelor's degree in Life Sciences
- 12+ years in scientific/pharmaceutical field
- Knowledge of regulatory, compliance, GMP, and laboratory testing
- Technical experience with FDA, EMA, PMDA, CFDA, and global regulations
- Understanding of end-to-end CMC processes and quality systems
- Leadership experience managing complex cross-functional issues
- Experience in method development and analytical instrument validation
- Budget and resource management skills
Nice to have
- Advanced degree (Master's or PhD)
- Experience authoring complex regulatory dossiers