CQV Validation Engineer; IQ/OQ/PQ; Pharma Manufacturing
Listed on 2026-10-07
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Engineering
Pharma Engineer, Validation Engineer, Quality Engineering, Biomedical Engineer -
Pharmaceutical
Pharma Engineer, Validation Engineer, Quality Engineering
Piper Companies is seeking an experienced CQV Validation Engineer in Raritan, NJ to support IQ/OQ/PQ activities for new instruments and equipment in manufacturing operations.
The role requires a Bachelor's in Engineering and 5+ years in pharmaceutical equipment commissioning/validation, with strong regulatory knowledge (FDA, EU, ICH), problem-solving, and cross-functional collaboration.
The following opportunity is for a CQV Validation Engineer (IQ/OQ/PQ) - Pharma Manufacturing with ZP Group.
Join us at ZP Group as our next CQV Validation Engineer (IQ/OQ/PQ) - Pharma Manufacturing in Raritan, NJ, United States.
We are currently recruiting a CQV Validation Engineer (IQ/OQ/PQ) - Pharma Manufacturing for our team in Raritan, NJ, United States.
This is a genuine opportunity to take on the CQV Validation Engineer (IQ/OQ/PQ) - Pharma Manufacturing role at ZP Group.
As a CQV Validation Engineer (IQ/OQ/PQ) - Pharma Manufacturing, you will play an important part at ZP Group in Raritan, NJ, United States.
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