Cure Talent are delighted to be recruiting for an experienced Validation Specialist to join a leading engineering function in the pharmaceutical and life sciences industry. This is a fantastic opportunity to apply your technical validation expertise in a dynamic and regulated environment focused on delivering high quality manufacturing solutions.

As a Validation Specialist, you will lead and execute validation activities across the full lifecycle, ensuring compliance with regulatory standards and industry best practices.

Key Responsibilities:

• Lead Commissioning, Qualification, and Validation activities across equipment, facilities, and computer systems
• Deliver robust Process and Cleaning Validation and ensure compliance with GMP standards
• Execute Computer System Validation in line with GAMP 5 and data integrity requirements
• Prepare and maintain validation documentation, including protocols, risk assessments, and reports
• Collaborate with QA, Engineering, IT, and Regulatory Affairs to support project and audit readiness

Role Requirements:

• Degree in a scientific or engineering discipline, or equivalent practical experience
• Extensive experience in validation roles within pharmaceutical or life sciences sectors
• Proven expertise in equipment qualification process validation, and CSV
• Strong understanding of GxP, EU GMP Annex 11, 21 CFR Part 11, and regulatory audit standards
• Excellent attention to detail, risk-based thinking, and ability to work independently or in teams

If you're an experienced validation professional looking to make a real impact in a forward-thinking organisation, apply now to take the next step in your career.