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| Job Location | Cambridge |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
Senior Manager / Associate Director GVP Pharmacovigilance Quality and Compliance for a Global Biotech in Cambs I am partnered with a global biotech giant based in Cambridge in the search for a senior Drug Safety/Pharmacovigilance compliance and quality auditor to join a high calibre team of pharmacovigilance/drug safety specialists in the pharmacovigilance quality and compliance auditing group - this will be a senior role involving both hands auditing as well as strategic responsibilities. This is a great opportunity for a seasoned drug safety/pharmacovigilance auditor to join an experienced team of auditors and help to them to maintain quality pharmacovigilance excellence throughout the business. In the role of a senior manager/associate director within the GVP quality and compliance group you will get the opportunity to be involved in all aspects of auditing across the business. You will be joining a high calibre team of experienced drug safety/pharmacovigilance auditors and will get the opportunity to audit one of the most innovative and interesting businesses currently operating in the biotech space. In order to hear more about this excellent opportunity to work with some of the top UK drug safety/pharmacovigilance auditors then send your CV to to make an initial application. Required skills
Keyskills :
audit compliance quality cambridge qa audit drug safety pharmacovigilance biotech capa gvp