Position Details
About this role
A role focused on supporting biologic drug substance manufacturing through process development, validation, and optimization at a biotech manufacturing facility.
Key Responsibilities
- Support process transfer
- Ensure process validation
- Optimize downstream processes
- Maintain GMP compliance
- Collaborate on manufacturing improvements
Technical Overview
Supports downstream bioprocessing, process validation, and GMP-compliant manufacturing; applies biologics technology; collaborates across manufacturing teams.
Ideal Candidate
The ideal candidate is a mid-level process engineer with 4+ years of experience in downstream bioprocessing, process validation, and optimization within biotech manufacturing, preferably familiar with biologics technology and GMP standards.
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 experience in downstream bioprocessing, No GMP or biologics background, Poor teamwork or communication skills
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