$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 quality risk management and compliance operations at a pharmaceutical manufacturing site, ensuring regulatory readiness and driving continuous improvement across quality systems. It suits experienced quality assurance professionals with pharmaceutical expertise who want to take on operational leadership in a regulated manufacturing environment.
Our summary, not Biogen’s wording. The full posting is on their site.
Skills this role names
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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
- Strong knowledge of cGMP regulations and global regulatory standards
- Experience with quality systems including risk management, change control, deviation management, and inspection readiness
- Ability to analyze complex data and make decisions under pressure
- Excellent communication, organizational, and stakeholder management skills
Nice to have
- Master's degree (MBA, MS, or similar) with relevant experience
- Experience leading site-wide or global quality risk management programs
- Strong background supporting regulatory inspections and audit responses
- Demonstrated ability to influence cross-functional teams and drive cultural change
- Advanced knowledge of quality metrics and data-driven decision making