$107,904 – $130,754
Listed on Bristol Myers Squibb’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role leads validation and commissioning efforts for a new radiopharmaceutical manufacturing facility, supporting the transition from construction through clinical and commercial operations. It suits experienced validation engineers who can independently manage complex GMP projects while mentoring others in a specialized biotech environment.
Our summary, not Bristol Myers Squibb’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- BS or MS in a scientific field or equivalent work experience
- 4–8 years in radiopharmaceutical or injectable GMP manufacturing
- 4–8 years of validation experience in a GMP environment
- Technical writing skills
- Understanding of regulatory guidelines for validation and risk management
- Ability to work independently and with teams in a GMP cleanroom environment
- Willingness to handle radioactive materials
Nice to have
- Experience with additional validation domains (process validation, QC assets, CSV, cleaning validation)
- Proficiency with AI tools to enhance productivity