CQV Process Equipment

QCS Staffing Ltd; New Jersey; On-site; USD 90,000 - 120,000; Full time

Job summary

Quanta Consultancy Services Ltd is seeking an experienced CQV Process Equipment professional for a 12-month contract in New Jersey. The successful candidate will serve as the technical SME for automated process equipment commissioning, ensuring alignment with GMP standards.

You will develop and execute Commissioning Execution Plans, author test documentation, and report directly to the Client C&Q Manager.

A Master's degree in Automation Engineering or a related field, along with extensive CQV roles in automated biopharma manufacturing, is required.

Qualifications

• 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.

Responsibilities

• 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.

Skills

CQV roles

Automated biopharma manufacturing

Process equipment and control systems

Automation platforms

Education

Master’s degree in Automation Engineering or related field

Job description

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! #LI-CP1