Pharma CQV Engineer: Validation Lead; Onsite Raleigh
Listed on 2026-10-07
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Engineering
Pharma Engineer, Quality Engineering, Validation Engineer, Regulatory Compliance Specialist
Verista is seeking a Senior CQV Engineer in the Raleigh/Durham area to lead validation activities for pharmaceutical manufacturing. You will design validation plans, conduct risk assessments, and maintain qualification documents as part of a collaborative project team.
Requirements include 4–6 years of CQV experience, a Bachelor's degree, strong communication, and the ability to work onsite. Travel up to 10–50% may be required; GMP experience is essential.
We are seeking a motivated Pharma CQV Engineer:
Validation Lead (Onsite Raleigh) to join Veristainc in Durham, NC, United States.
Step into the Pharma CQV Engineer:
Validation Lead (Onsite Raleigh) role at Veristainc in Durham, NC, United States and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
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