GMP Validation Specialist

Job Description

ROLE OVERVIEW

We are supporting a leading Biopharmaceutical company who are seeking a GMP Validation Specialist to join their team based in Surrey. As the GMP Validation Specialist, you will play a pivotal role in ensuring the compliant status of the facility, equipment, utilities, and scientific process systems.

KEY DUTIES AND RESPONSIBILITIES

Your duties as the GMP Validation Specialist will be varied; however, the key duties and responsibilities are as follows :

1. Support the development, implementation, and ongoing maintenance of the Validation Strategy, ensuring alignment with regulatory expectations and industry best practices.
2. Coordinate and execute qualification and validation activities across the facility, including Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
3. Draft and update Standard Operating Procedures (SOPs), validation protocols, and reports, translating regulatory requirements into practical and clear procedures.
4. Act as a key point of contact for external suppliers, contractors, and service engineers during validation and qualification work, supporting internal and external audits and regulatory inspections.

ROLE REQUIREMENTS

To be succ…