Job Description

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.

Required Knowledge, Skills, and Abilities

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.