Description
A multinational pharmaceutical company require a QA Specialist/Senior Quality Officer for their UK facility. The company is dedicated to the discovery and development of innovative drugs for patient care in targeted therapeutic areas such as oncology, endocrinology and neuromuscular disorders. The UK manufacturing and supply site operates under a progressive management philosophy to current Good Manufacturing Practice guidelines.-As part of the unit 12 program it is possible that some QA resource for a period of 6 months - looking at the end of April as a start date.
-The ideal candidate should be at a Quality specialist / Senior QA Officer level:
-Ideally have sterile experience and be familiar with Qualification document review and approval as a minimum.
-Work with aseptic processes and Isolator technology would be a plus as would the ability to work flexible hours.
-The role will require input and review of project documentation, especially Qualification documentation so this role will involve checking of raw data associated with executed validation exercises.
-The person will also be expected to ensure GMP quality systems are adhered to and that project activities meet GMP expectations.
This is a contract opportunity for an inital six months, please apply for further details.