Interim Validation Manager

Walker Cole International is seeking an experienced and detail-oriented Validation Manager to oversee and manage all validation activities for an exciting pharmaceutical company based in the UK.

As the Validation Manager, your responsibilities will include:

• Develop, implement, and maintain validation master plans, protocols, and reports for equipment, facilities, utilities, cleaning, and computer systems.
• Lead and manage validation projects in accordance with cGMP, FDA, EMA, and other relevant regulatory guidelines.
• Ensure validation documentation (IQ/OQ/PQ, risk assessments, etc.) is accurate, complete, and audit-ready.
• Oversee the execution and review of validation protocols and reports for equipment, processes, and systems.
• Maintain validation schedules and ensure timely re-validation in accordance with established procedures.
• Serve as the SME for both internal/external audits related to validation.

To be successful as the Validation Manager, you will have:

• Bachelor’s degree in Engineering, Life Sciences, or a related field (Master’s preferred).
• 10+ years of experience in validation in a regulated environment (e.g., pharmaceutical, biotechnology, medical device).
• Strong knowledge of validation principles, including GAMP 5, risk-based validation, and regulatory requirements (FDA 21 CFR Part 11, EU Annex 11, etc.).
• Experience with validation of automated systems, laboratory equipment, manufacturing processes, and cleaning procedures.
• Excellent organizational, communication, and leadership skills.

Contract Details:

• Length of assignment: 6 month contract 
• 5 days onsite - Full-time
• Location: United Kingdom
• Pay: Daily 
• Start date: ASAP

Validation l Qualification l CQV l C&Q l  Manager l Team Lead l Supervisor l GMP | Good Manufacturing Practice | Interim l Contract l Contractor l Pharmaceutical | Pharma l CDMO l