Position Details
About this role
This role involves supporting manufacturing systems and labeling operations for cell therapy production, ensuring compliance and operational efficiency.
Key Responsibilities
- Support labeling system lifecycle
- Manage validation processes
- Lead change management initiatives
- Ensure compliance with cGMP
- Optimize boundary systems
Technical Overview
The position requires expertise in manufacturing execution systems, validation, boundary systems, and cGMP standards within biotech manufacturing environments.
Ideal Candidate
The ideal candidate is a mid-level manufacturing systems engineer with 3+ years experience in MES and labeling operations, preferably with biotech or pharmaceutical manufacturing background, capable of supporting validation and change management processes.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
No experience with manufacturing execution systems, Lack of biotech/pharmaceutical manufacturing background, No validation or change management experience
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