Position Details
About this role
Engineer III, Manufacturing Sciences - Purification provides technical and process expertise to support technology transfers and ongoing clinical and commercial manufacturing operations in a cGMP environment.
Key Responsibilities
- Serve as the downstream/purification technical lead for manufacturing issues during clinical, PPQ, and commercial processing
- Plan, execute, analyze, and communicate purification studies
- Perform data trending and statistical analysis
- Observe and support critical downstream/purification operations
- Author and review GMP documentation
Technical Overview
Focus on downstream purification processes (chromatography, filtration, centrifugation); utilizes analytics tools (Tableau, Power BI, Statistica, SIMCA) for data trending and process improvement; collaborates across manufacturing, QA, and technical teams.
Ideal Candidate
The ideal candidate is a self-driven purification engineer with 2+ years of industry experience in chromatography, filtration, and centrifugation, proficient in GMP/cGMP environments and cross-functional collaboration.
Must-Have Skills
None listed
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
No cGMP manufacturing experience, Lack of ability to work in a cGMP environment, No Bachelor's degree or equivalent
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