What you’d do
Lead integration of bioconjugate manufacturing scope for a client facility project, coordinating stakeholders, contractors, suppliers, and C&Q teams from design through startup and transition to GMP operations. Full time. Found on the employer's careers page on Oct 19, 2026. Apply through the link.
You’ll need
- Bachelor's in engineering or related technical discipline
- 15+ years engineering experience
- Pharma/biotech or GMP-regulated facility experience
- Managing large multidisciplinary engineering teams
- Managing engineering contractors
Our summary of the listing. The full listing has the details.