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.
Required Knowledge, Skills, and Abilities
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.