Description
The purpose of this job role is to assure that Suppliers of Materials, Service Suppliers and Third Party Operations within the scope of QA&C meet applicable GSK and Regulatory requirements.
Key Responsibilities:
- Perform Quality System assessments of assigned audits within role scope
- Make risk-based recommendations on GxP approval status and document assessments in relevant systems
- Ensure transparent communication with business stakeholders on audit progress and potential issues
- Agree on corrective and preventive action (CAPA) plans and follow up on completion
- Maintain audit and user site data in GSK supplier management system
Requirements:
- At least 10 years of experience in a pharmaceutical/Biological environment
- Proficiency in planning and executing audits to identify and reduce significant risks/non-compliances
- Knowledge of regional/global GMP and GSK quality requirements
- Good verbal and written communications skills
- Proficiency in verbal and written English
- Experience with Microsoft Office applications
Education:
- Post Graduate/Graduate degree in relevant Science (Biology, Chemistry, Pharmacy) or Food/Chemical/Biotechnology or equivalent Engineering area of expertise
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