Experienced CQV Engineer Biotech and Pharmaceutical Projects

Position: Experienced CQV Engineer for Biotech and Pharmaceutical Projects
Drive successful CQV operations in pharmaceutical and biotech manufacturing. This hands-on, field-focused role requires expertise in commissioning, qualification, and validation within GMP environments.

As a CQV Engineer, you will support various project tasks, including executing validation protocols and managing equipment handovers. Strong knowledge in utilities, process equipment, and hands-on experience in regulated settings are key. You’ll collaborate closely with QA, Automation, and Engineering teams to maintain compliance with GMP standards.

Key Responsibilities:

• Prepare and execute CQV protocols for systems

• Perform functional testing and equipment handover

• Manage FAT/SAT and issue resolution tasks

• Document and report deviations effectively

• Ensure compliance with cGMP and ASTM E2500

Requirements:

• 5+ years in CQV for GMP-regulated facilities

• Bachelor’s degree in Engineering or Life Sciences

• Proficient in electronic validation tools

• Strong knowledge of P&IDs and engineering documentation

• Excellent communication and organizational skills

Utilize your CQV expertise to support quality and compliance within dynamic pharmaceutical environments.
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