CQV Engineer - On-site Validation Specialist; Devens
Listed on 2026-10-11
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Engineering
Quality Engineering, Validation Engineer, Pharma Engineer
Verista is hiring a Validation Engineer for a full-time, on-site position in Devens, MA. The role requires expertise in executing IQ/OQ protocols and supporting commissioning activities, ensuring compliance with GMP/GDP practices.
Candidates must hold a Bachelor’s in a related field and have 1-3 years of experience in a pharmaceutical, biotech, or regulated environment. The position offers a robust benefits package including competitive pay, health insurances, a 401(k) plan, and paid parental leave.
We have an opening for a CQV Engineer
- On-site Validation Specialist (Devens) in Harvard, MA, United States within Engineering.
This opportunity is for the CQV Engineer
- On-site Validation Specialist (Devens) role at Verista.
We are seeking a motivated CQV Engineer
- On-site Validation Specialist (Devens) to join Verista in Harvard, MA, United States.
Consider building your career as a CQV Engineer
- On-site Validation Specialist (Devens) at Verista.
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