I have an excellent opportunity as a Process Validation Associate for a leading and rapidly growing global biopharmaceutical company.

You will be driving validation and qualification activities for the systems, processes and equipment to ensure GMP compliance.

This role will offer you

• To act as a Validation and Qualification subject matter expert within a global business
• Strategic input for qualification and validation
• Exposure to cutting-edge projects which have the real potential to save and improve peoples lives
• Work at the forefront of science

You will be responsible for

• Qualification and validation of systems, processes and equipment
• Qualification activities ensuring compliance with GMP and HSE regulations and in accordance with the site Validation Master Plan
• Holding periodic reviews - Following up on qualification activities and developing validation/qualification strategy
• Working closely with quality, supporting internal audits, external audits and regulatory inspections

You will bring the following

• 2 years Qualification and Validation experinece within GMP pharmaceuticals
• French is required as well as good knowledge of English
• MSc in a relevant Life Sciences subject

If you want to be part of an innovative thinking, growing company where you can grow and expand your current knowledge, GET IN TOUCH