Job Responsibilities
• Ensure adherence to all incoming materials procedures
• Reviews logbooks as per the procedures and ensures compliance.
• Oversight on sampling and dispensing activities.
• Handling of Quality Notifications (QN)
• Approval / Rejection of incoming materials
• Handling of investigations, change controls and CA/PAs.
• Review and approval of consumables specifications
• Handling of incoming material dispositions and blocking materials in SAP
• Verification of sampling, material dispensing and issuance of consumables as per procedures.
• Compliance to Pfizer integrity principles at all stages of operations.
• Participate in external (Regulatory and Non-regulatory) audits.
M.Pharm/M.Sc ; Minimum of 3 year pharmaceutical manufacturing/Quality experience
Experience: 3 years
Location: Visakhapatnam
Education: M.Sc, M.Pharm
Industry Type: Pharma/ Healthcare/ Clinical research
Functional Area: QA
Job ID: 1613783
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