Process Validation Engineer
Quick Summary
Control Strategies: Contribute knowledge and technical expertise to the development and refinement of manufacturing control strategies for oligonucleotide unit operations (examples: synthesis,
Support continued process verification, which may include but is not limited to leading Continued Process Verification (CPV) plans, authoring CPV reports, and reviewing Product Quality Reports.
Agilent Technologies Advanced Therapeutics Division (previously Nucleic Acids Solutions Division) is looking for a Process Validation Engineer to join their Process Validation team working at their state-of-the-art, contract Active Pharmaceutical Ingredient manufacturing facility that specializes in oligonucleotide chemistries located in Boulder and Frederick, Colorado.
Responsibilities
~2 min readLocation & Eligibility
Listing Details
- Posted
- June 24, 2026
- First seen
- July 6, 2026
- Last seen
- July 6, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 18%
- Scored at
- July 6, 2026
Signal breakdown
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