Validation Specialist

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We are supporting a leading Biopharmaceutical company that is 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.

• Support the development, implementation, and ongoing maintenance of the Validation Strategy, ensuring alignment with regulatory expectations and industry best practices.
• Coordinate and execute qualification and validation activities across the facility, including Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
• Draft and update Standard Operating Procedures (SOPs), validation protocols, and reports, translating regulatory requirements into practical and clear procedures.
• 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.

• Relevant degree in life sciences or a related field.
• Proven industry experience in GMP principles and validation methodologies.
• A working knowledge and practical experience with drafting SOPs, validation protocols, and conducting risk assessments.

GMP, Validation Specialist, Quality Assurance, CVIM, Process Team, Validation Strategy, Qualification Activities, Regulatory Compliance, SOPs, Risk Assessment, Life Sciences.

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.