Job Description:
The client is in need of a Validation Engineer who can write and run protocols for Product Manufacturing companies. The client does NOT want a validation engineer who only has experience working on lab or diagnostic equipment. This person will have to jump in quickly to respond to FDA citations, they will be writing the batches records (1 day per batch), writing the report and testing the process. The candidate will be responsible for creating a Validation Master Site Plan. The perfect resume will have experience with OTC and Gel Product companies working on Validation Process Documents.
Skills:
- 8-10 years of GMP experience
- Validation and Process Background for Product. NOT for lab for diagnostic equipment
- Remediation background is preferred. Or working in a small high paced environment
- Batch record review, SOP review, Writing and reviewing Val Protocols
- Writing Validation Site Master Plans
- Plus: Nasal Spray Product Experience
Remote: Senior Validation Engineer (232969)
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