Senior Validation Engineer - Biopharma GMP Specialist
Listed on 2026-10-06
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Quality Assurance - QA/QC
Quality Engineering
KBI Biopharma, Inc. is seeking a Level II Validation professional to facilitate the validation lifecycle across multiple disciplines in a multi-product facility. You will coordinate validation testing, contribute to change control, and support business efficiency projects.
The role requires a Bachelor’s in a scientific/biochemical engineering field with 5+ years in fermentation/cell culture environments, plus strong Quality Systems and cGMP knowledge.
We would love to welcome a new Senior Validation Engineer
- Biopharma GMP Specialist to our organisation in Boulder, CO, United States.
Learn more about the Senior Validation Engineer
- Biopharma GMP Specialist role in the description above.
We appreciate your interest in this position.
Join KBI Biopharma, Inc. and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
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