Validation and Compliance Specialist

Validation and Compliance Specialist required for a permanent role based in Manchester. This position involves overseeing quality compliance and validation protocols within a busy biopharmaceuticals environment. The successful candidate will ensure all processes meet strict industry regulations while supporting ongoing facility improvements.

Responsibilities

• Develop and implement validation master plans for biopharmaceutical processes.
• Conduct regular compliance audits to ensure adherence to regulatory standards.
• Oversee the validation lifecycle for equipment, utilities, and analytical methods.
• Manage deviations and non-conformances through robust CAPA investigations.
• Collaborate with cross-functional teams to maintain site inspection readiness.
• Provide technical guidance on GxP compliance and quality risk management.
• Draft and review standard operating procedures and validation reports.

What you'll need

• Extensive experience in validation within a biopharmaceutical or life sciences setting.
• In-depth knowledge of MHRA and FDA regulatory requirements.
• Proven ability to manage complex validation projects and compliance audits.
• Strong analytical skills for evaluating technical data and process performance.
• Excellent written and verbal communication skills for technical reporting.
• Right to work in the UK.
• Relevant degree in life sciences, engineering, or a related discipline.