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