Validation Associate

4 weeks ago


Dartford, Kent, United Kingdom Catalent Full time

At Catalent, we're committed to delivering high-quality products to patients around the world. As a Validation Associate, you'll play a critical role in ensuring the quality and integrity of our pharmaceutical products.

The Role:

  • Develop and maintain the site Validation Master Plan, ensuring compliance with cGMP regulations and company standards.
  • Coordinate equipment validations, including new lab instrumentation and operations equipment.
  • Participate in Validation History Reviews to ensure validation practices are up-to-date and compliant.
  • Review Process and Analytical Development reports to assess product suitability for validation.
  • Provide technical guidance on process deviations and equipment performance.
  • Manage a Quality Management system, including training, SOPs, internal audits, and document archiving.
  • Ensure completion of GMP documentation and deviation investigations in accordance with Data Integrity requirements.

Requirements:

  • Graduate in Pharmaceutical Sciences or equivalent experience.
  • Experience in leading validation in a cGxP environment, with strong knowledge of cGMP regulations.
  • Experience in managing multiple projects and executing validation protocols.
  • Experience working in a cGMP environment.

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law. If you require reasonable accommodation for any part of the application or hiring process, please submit your request by sending an email to .


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