Performing GMP/Quality System assessments/audits of assigned suppliers
Making risk-based recommendation on supplier GMP approval status
Documenting assessments/audits in relevant systems
Agreeing appropriate corrective and preventive action (CAPA) plans with suppliers
Follow-up on the completion of CAPAs within agreed timelines
Effective communication of assessment outcomes to internal and external stakeholders
Ensuring audit-related documentation is effectively communicated
Maintenance of auditee (supplier) profiles in data systems
Collating identified risks and escalating high risk issues/situations

Relevant experience (ideally gained from the working in a highly regulated environment like Pharmaceutical Manufacturing)
Degree in Life Science or other relevant disciplines
Knowledge of current GMP requirements within major pharmaceutical markets
Knowledge and application of the principles of the Quality Management Systems (QMS)
Comfortable with verbal and written English.

Supplier Quality Auditor

Key skills