Position Details
About this role
This role supports the design, commissioning, and qualification of equipment and facilities in a sterile drug manufacturing environment, ensuring compliance with GMP standards.
Key Responsibilities
- Support equipment design
- Assist in facility startup
- Conduct commissioning and qualification
- Perform risk assessments
- Ensure GMP compliance
Technical Overview
The position involves working with aseptic processing equipment, facility commissioning, and qualification activities to enable sterile manufacturing operations.
Ideal Candidate
The ideal candidate is an entry-level engineer with foundational knowledge of aseptic processing, equipment qualification, and sterile manufacturing, eager to support facility startup and operational readiness in a biotech environment.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of aseptic or sterile manufacturing experience, No familiarity with GMP standards, Inability to work in a team environment
Get matched to jobs like this
Luna finds roles that fit your skills and career goals — no endless scrolling required.
Create a Free Profile