Talentmark are working in partnership with a leading UK life sciences biotechnology company, to recruit  a Senior QA Auditor with GCLP audit experience, to join them at their site based in London.  This is a permanent role with flexibility of hybrid working (3 days on-site).

The Role:
The successful candidate will be supporting with regulatory training, eQMS and QA projects. They will also be responsible for ensuring the client are in compliance with the relevant SOPs, regulations and internationally recognised guidelines (GCLP).

Other Responsibilities Include:

Plan and conduct audits of processes, facilities, documents and systems in order to deliver the audit programme as required by GCLP
Assist with Hosting external sponsor audits and regulatory inspections
Act as Lead Auditor to plan, conduct and follow up on-site audits of suppliers and subcontractors
Identify and assess Quality Management System (QMS) non-compliancesYour Background:

Degree qualified in a relevant scientific subject. Further qualification in Quality would be desirable.
GCP for laboratories experience within industry environment i.e. GCLP
Quality assurance auditing and quality system experience within industry
Experience in supporting regulatory inspections and client audits
Proven knowledge of drug development processesApply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.
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