Position Details
About this role
This role involves leading process development and optimization for sterile drug products, ensuring GMP compliance, and supporting technology deployment in a pharmaceutical manufacturing environment.
Key Responsibilities
- Develop and optimize sterile processes
- Troubleshoot manufacturing issues
- Lead equipment and facility improvements
- Ensure GMP compliance
- Support process scale-up
Technical Overview
The position requires expertise in sterile processing, equipment and facility optimization, GMP standards, troubleshooting, and process scale-up, with a focus on continuous improvement and regulatory adherence.
Ideal Candidate
The ideal candidate is a mid-level process engineer with 7+ years in sterile drug processing, equipment and facility optimization, and GMP compliance. They should demonstrate leadership, troubleshooting skills, and experience in pharmaceutical or biologics manufacturing.
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 sterile drug processing, No GMP experience, Unwilling to work in Rahway, NJ
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