Job Description

Job Responsibilities Responsible to ensure adherence to all quality procedures and material management procedures. Review logbooks/electronic log as per the procedures and ensures compliance. Ensures that analytical report compliance to relevant regulations, standards and site/global procedure. Usage decision (Acceptance/ Rejection) of incoming materials, in-process & finished products (P1, P2, and P3) Review of warehouse equipment\'s alarm trends and temperature excursions, area temperature excursions review and approval. Review of consumables specifications. Review of Protocols and APQR\'s. Handling of incoming material restriction, un-restriction and blocking materials in SAP part of investigation recommended disposition. Evaluation of new consumable materials and certification. Compliance to Pfizer integrity principles at all stages of operations. Perform walkthroughs at warehouse. Provides Quality oversight for warehouse activities-Dispensing, Sampling, Material management etc. Inspection of material damages. Review of change controls impact assessment related to material management. Timely closure of AMPS exceptions. Qualifications Must-Have B. Pharm/M. Pharm/M.Sc. 6-8 years of experience in Manufacturing Quality Assurance / Quality Assurance / Quality Control of a pharmaceutical manufacturing facility. Knowledge of current Good Manufacturing Practices Good communication and interpersonal skills Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Quality Assurance and Control#LI-PFE

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