Job Description

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.

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

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 license is essential, as travel to other sites may be required.