Validation Engineer
- Strong IQ/OQ/PQ execution experience - Must be able to write and execute validation protocols independently in a GMP environment.
- GMP / GxP compliance knowledge - Solid understanding of FDA-regulated pharma manufacturing and documentation standards.
- Hands-on equipment & process validation - Experience validating manufacturing systems and ensuring consistent performance.
- Validation documentation & reporting - Skilled in writing protocols, reports, and handling deviations/change controls.
- (Nice-to-have) Packaging validation experience - Exposure to packaging lines, serialization, or related validation is a bonus but not essential.
Packaging line qualification (IQ/OQ/PQ)
Experience validating blister lines, bottling lines, or filling/finishing packaging equipment.Seal integrity & container closure integrity (CCI)
Understanding of ensuring packaging maintains product sterility and stability.Labeling & serialization systems validation
Experience with label control, barcode systems, and track-and-trace/serialization compliance.Transport & distribution validation
Ability to validate packaging performance through shipping studies (temperature, vibration, etc.).Material qualification
Working with packaging components (e.g., vials, syringes, cartons, films) to ensure they meet regulatory and product requirements.
- ASAP start
- 6/12 months potentially longer
- Onsite in Columbus, Ohio
- 40 hours a week
- W2 only
If this is something you are interested in please send your CV
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