Responsibilities:

• Lead facility and equipment CQV processes
• Prepare and execute IQ, OQ, and PQ protocols
• Ensure compliance with GMP validation standards

Requirements:

• Hands-on experience in CQV within pharma facilities
• Familiar with GAMP and validation lifecycle processes
• Ability to manage complex technical projects

What’s on Offer:

• Engage in high-impact biopharma facility projects
• Work remotely or travel depending on project needs
• Be part of transformative healthcare infrastructure development