Position Details
About this role
This role involves leading process development and quality investigations in a sterile GMP pharmaceutical manufacturing environment, supporting facility startup and regulatory compliance.
Key Responsibilities
- Lead process tech transfer
- Ensure GMP compliance
- Support facility startup
- Conduct quality investigations
- Develop SOPs
Technical Overview
The technical scope includes GMP manufacturing, process transfer, scale-up, quality investigations, SOP development, and regulatory compliance within pharmaceutical or biotech settings.
Ideal Candidate
The ideal candidate is a mid-level sterile process engineer with over 5 years of experience in GMP manufacturing, process transfer, and quality investigations, with a strong background in pharmaceutical sciences or chemical engineering.
Must-Have Skills
Nice-to-Have Skills
Required Skills
Hard Skills
Soft Skills
Industry & Role
Clearance & Visa
Keywords for Your Resume
Deal Breakers
No experience with GMP or sterile manufacturing, Lack of relevant scientific degree, Less than 5 years of relevant experience
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