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Validation Specialist

1 month ago

London, United Kingdom Hobson Prior Full time

Hobson Prior has partnered with a biotechnology company who is seeking a Validation Specialist to join our clients team in London. In this role, you will support the Engineering department to ensure our gene therapy manufacturing activities comply with validation standards.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Help qualify equipment and systems for manufacturing, quality control, and engineering.
  • Review and approve validation documents from external sources.
  • Write validation documents.
  • Oversee the execution of validation protocols.
  • Complete validation summary reports.
  • Collaborate with various departments to ensure timely delivery of qualification reports and closure of quality records.
  • Assist with system and equipment documentation using a risk-based approach.
  • Manage validation reviews and re-qualifications to maintain compliance.
  • Support computer system validation and compliance where needed.

Key Skills & Requirements:

  • Strong problem-solving abilities.
  • Leadership and motivational skills.
  • Effective planning and organizational skills.
  • Commitment to quality management and innovation.
  • Excellent oral and written communication skills.
  • Practical skills in validation tasks.
  • Ensure compliance with GMP, Data Integrity, and Good Documentation Practice.
  • Complete training in a timely and compliant manner.
  • Ensure timely closure of GMP documentation.

For more information, please contact William Hay at

Apply now

If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively for further details or to talk directly to a life sciences recruitment specialist directly please select 'Contact me' at the top of this page.

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