I have an excellent opportunity as a Validation Specialist for an innovative and rapidly growing cell and gene organisation based in London, giving you a chance to work in a fast-paced environment and the ability to make a huge impact.

This opportunity will allow you to take on a critical role in Quality & Validation providing a hands-on SME role in Qualification and Validation (Q&V) in line with GMP regulations.

This role will offer you:

• Exposure to numerous clinical projects and products which have the potential to save lives
• Exposure to high visibility from the senior leadership team
• Opportunity to join one of the most rapidly expanding biopharmaceutical company
• Work at the forefront of science

You will be responsible for:

• Anything related to qualification and validation in support of Quality and safety
• Supporting the Pharmaceutical Quality Management System (PQMS) in relation to Qualification/Validation strategies
• Drafting and reviewing Q&V documentation

You will bring the following:

• Minimum 3 years experience working in a Pharmaceutical GMP setting
• Life science degree or equivalent
• Validation and Qualification experience
• Must have experience working with Steriles, Cleanrooms, or Aseptics