CQV Process Equipment

CQV Process Equipment - US, New Jersey - 12 Month Contract

Our client is a world‑leading pharmaceutical powerhouse, operating across more than 60 countries and driving innovation at every stage of the drug development lifecycle. This progressive, future‑focused organisation is now searching for an experienced CQV Process to play a key role in a high‑impact project based in New Jersey.

What you’ll do:

• Serve as the technical SME for automated process equipment commissioning.
• Report directly to the Client C&Q Manager, representing the owner’s interests across all project phases.
• Develop and execute Commissioning Execution Plans with a focus on automation, data integrity, and system interoperability.
• Author and review commissioning and qualification protocols and test documentation for automated systems, ensuring alignment with URS, GMP, and EHS standards.

What you’ll need:

• Extensive experience in CQV roles within automated biopharma manufacturing.
• Hands-on experience with automated process equipment and control systems.
• Strong understanding of validation lifecycle and automation platforms.
• Master’s degree in Automation Engineering or related field.

If this role is of interest, apply now!

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