Validation Specialist

Validation Specialist - UK, Oxford - 11 Month Contract

Are you aValidation Specialist professional with experience in Oxford? Are you looking to take the next step in your career and be part of an exciting new project? Then the position ofValidation Specialist is exactly what you're looking for.

This is your chance to work for a company that is a pioneer in gene and cell therapy focusing on long-term curative treatments. With vast investment being made into the organisation and new build projects on the horizon this is the ideal time to join the team and establish yourself as a key team member.

Led by an experienced executive team, this is a fantastic opportunity to work for a high-profile Biopharma client.

Responsibilities:

• Revise and reformat existing URS documents using client's internal templates.
• Author and review DQ and RTM documentation.
• Support validation of 9 high-complexity systems, including isolators and filling lines.
• Provide validation input for bioreactors and chromatography systems.
• Assist with validation of 40+ medium and low-complexity systems (e.g., benchtop equipment).
• Contribute to small-scale projects and ongoing validation activities.
• Collaborate with internal teams to ensure MHRA compliance following previous audit feedback.

Requirements:

• Extensive experience in validation documentation roles within a biopharma environment.
• Strong understanding of GMP and MHRA expectations.
• Proactive, personable, and capable of working independently.
• Not essential, but relevant qualifications are a plus.

If this role is of interest, apply now.