Position Details
About this role
This role provides on-site engineering support for sterile manufacturing facilities, ensuring GMP compliance, troubleshooting equipment, and supporting validation activities for sterile products.
Key Responsibilities
- Support sterile operations
- Ensure GMP compliance
- Troubleshoot equipment
- Manage validation lifecycle
- Support capital projects
Technical Overview
The technical scope includes GMP standards, sterilization and cleaning validation, equipment troubleshooting, and supporting validation lifecycle in a pharmaceutical environment.
Ideal Candidate
The ideal candidate is an experienced engineer with a background in sterile operations, GMP compliance, and equipment validation, capable of troubleshooting and supporting validation lifecycle in a pharmaceutical manufacturing environment.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Clearance & Visa
Keywords for Your Resume
Deal Breakers
Lack of GMP or sterile operations experience, No equipment troubleshooting skills, Inability to work on 2nd shift
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