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Validation Engineer
Job in
Newark, Essex County, New Jersey, 07175, USA
Listed on 2026-06-07
Listing for:
Global Compliance Partners
Contract
position Listed on 2026-06-07
Job specializations:
-
Pharmaceutical
Pharma Engineer, Validation Engineer
Job Description & How to Apply Below
Global Compliance Partners (GCP) is a GxP and GMP compliance consulting firm with over a decade of experience supporting biopharma and cell & gene therapy organizations. We partner with leading drug developers and manufacturers to deliver validation, quality, and compliance solutions, from CSV/CQV and process validation through tech transfer and BLA support. Our consultants embed directly with client teams to move programs forward with rigor and speed.
We are staffing an active client engagement and seeking experienced CQV Engineers to join our team. This is a 6-month contract with an immediate start.
Responsibilities- Execute commissioning, qualification, and validation activities (IQ/OQ/PQ) for GMP equipment and automation system
- Author and review validation protocols, manage deviations, and drive execution deliverables on a fast-moving timelin
- Partner closely with client quality and engineering teams on-site
- Demonstrated CQV experience in a GMP environment (biologics or cell & gene therapy a plu
- Hands‑on protocol execution with strong documentation discipli
- Able to work on‑site in New Jersey (some flexibility on days per wee
- Adaptable, accountable for deliverables, and effective when timelines move fa
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