Company: Teva Pharmaceuticals
Location: Goa, IN, 403722
Qualifications
B.Sc/M.Sc in chemistry/ life science/B/M Pharm with 9-12 years of experience in Quality Compliance and Vendor Qualifications
Function
Quality
Sub Function
Job Description
- Ensure the implementation of Standard Operating Procedures relating to the Site activities and compliance with the requirements of Good Manufacturing Practice (cGMP)
- Ensure the inspection readiness program at site
- Review and approves documentation related to compliance and inspection readiness
- To assure the continuous improvement in the quality of the Site activities
- Oversee the implementation of corporate standards at site
- Responsible for external audits (including inspection by health authorities) and provides all relevant data
- Ensure CAPA actions/commitment to regulatory inspections, customer inspection and self-inspection are effectively implemented at site
- Oversee the correct implementation of the change control procedure so as to assess and prevent unintended adverse consequences resulting from changes
- Participates in Knowledge sharing session and ensure implementation of best practices at site
- Ensure availability of validation master plan and site master file as per current requirement
- Responsible for site quality councils
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