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Senior Validation Engineer
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- Write engineering and design specifications (URS/FS/DS) and protocols (IQ/OQ/PQ/CSV) for facility and utility systems.
- Perform (hands on) field execution of commissioning and/or validation documentation.
- Strong utility and facility commissioning, qualification and validation experience.
- Experience with FDA compliance and cGMP is required.
- Must be results oriented with several years of hands-on experience, familiar with industry concepts, practices, and procedures in a cGMP environment.
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