GMP QA Auditor

CK Science are recruiting for a GMP QA Auditor to join a leading CRO company at their site based near Northwich (Cheshire) on a permanent basis.

Location:
This role will be based at their site in Northwich and Knutsford and will involve travel to and from clients on the audit schedule.

GMP QA Auditor Role:
To plan, organise and report internal and external audits in support of the company audit schedule and to other client organisations.

Key Responsibilities:

- Planning and scheduling of GxP audits.
- Completion of audits by visiting relevant sites, interviewing staff and reviewing documentation.
- Conduct internal audits/vendor audits.
- Participate and lead internal/external projects including gap analysis, QMS developments and QA support.

Your Background:

- Bachelor's degree, or equivalent, in a science subject.
- A minimum of two years GLP or GMP auditing experience, preferably in a pharmaceutical or clinical trial environment.
- Experience of planning, performing and reporting an audit within a pharmaceutical environment.
- A strong understanding of clinical processes.
- Full UK Driving Licence is essential, as travel to other sites may be required.

Apply:
For more information or to apply for this GMP QA Auditor position, please contact Naynesh on 01246 457703 or email nmistry@ckscience.co.uk, quoting job ref 48847.

It is essential that applicants hold entitlement to work in the UK.

INDGEN