We are looking for a Validation Specialist to join a large greenfield project in the Pharmaceutical sector.
This role will take responsibility to manage and execute the Master Validation Plan. The successful candidate will review, author and execute IQ/OQ/PQ on all GMP equipment. Duties will also include performing technical reviews, manage suppliers/contractors/vendors, and conduct system administration activities. Ultimately, this position will take the leadership in delivering validation on time and within budget for this facility.
Validation Specialist experience required:
- Experience within a similar role
- Ability to demonstrate a portfolio of projects delivered successfully on time and within budget
- Excellent working knowledge of FDA regulations
- Strong communication skills with experience in a leadership role
- Must be eligible to work in the USA
If you meet the criteria, please do not hesitate to contact Biotech Rec for further details or to be considered for the role.
Please note, Biotech Rec do not sponsor Visa applications.