CQV Lead (Pharmaceutical)

TL;DR

CQV Lead (Pharmaceutical): Coordinating and executing validation activities for pharmaceutical facilities and equipment with an accent on GMP compliance and validation documentation. Focus on managing the validation team, overseeing cleaning validation, and ensuring efficient execution of protocols for bioreactors and isolators.

Location: Onsite 4 days a week in Kent, United Kingdom

Company

hirify.global is a professional services firm providing project management and engineering solutions for the pharmaceutical and biotech industries.

What you will do

• Manage day-to-day operations of the Validation Team, including planning, prioritization, and execution of activities.
• Coordinate validation for facilities, equipment, and processes to ensure full compliance with GMP standards.
• Develop, execute, and complete critical validation documentation, including protocols and final reports.
• Collaborate closely with Engineering and Quality Assurance departments to align validation goals.

Requirements

• BSc in Engineering, Science, or an equivalent degree.
• Proven experience in CQV at a Lead or Managerial level.
• Professional background within the pharmaceutical industry.
• Hands-on experience with bioreactors, SIPs, CIPs, homogenisers, and disk stack centrifuges.
• Expertise in cleaning validation, Grade A isolators, and media fill (APS).
• Must be based in or able to work onsite in Kent, UK.

Culture & Benefits

• 6-month contract duration.
• Engagement structure: Outside IR35.
• Immediate start available.