Assistant Manager, Enterprise Quality Auditing @ Crescendo Manpower

Job Description

Job Description Summary This job position is responsible to perform audits globally for vendors [Sterile API, Packaging (Sterile / Non-Sterile), Excipients & Sterile Consumables] and service provider as a part of vendor qualification program. Responsible to perform audits of external CMO (Contract Manufacturing Organization) for sterile manufacturing - SVP (Small Volume Parental), LVP (Large Volume Parental), Biologics & combination products globally as per the current guideline requirement. Responsible for ensuring GMP compliance at site by executing corporate audits of Endo Sterile formulations sites as an SME for sterile operation. Job Description Perform external vendor audits pertains to Sterile API, Packaging (sterile and non-sterile), sterile consumables & Excipient. Perform external CMO audits for sterile manufacturing - SVP (Small Volume Parental), LVP (Large Volume Parental), Biologics & combination products globally as per the current guideline requirement. Perform service provider audits of Contract Service Provider & contract packaging. Ensuring GMP compliance at site by executing corporate audits of Endo Sterile formulations sites. Timely escalation to the management for any risk noticed during audit. Ensure implementation of CAPA for the performed audit in timely manner. To review and ensure all documentation pertaining to Vendor qualification of suppliers, consumable & service provider for all PAR India sites particular to sterility assurance. To execute, review and follow-up for completion of technical agreement pertaining to supplier & service provider. Approving and maintaining the manufacturer/ supplier in SAP. Handle respective QMS documentation within this function. To support manufacturing site as sterile SME during regulatory inspection. Education & Experience: Master's in science (Microbiology) / Master in Pharma. Microbiology is preferable. Hands on experience in sterile formulation unit (Manufacturing, Quality, Sterility Assurance & Validation). Experience in vendor (Sterile and Non-sterile) auditing & supplier qualification Minimum experience: 10 to 14 Years Commitment to Diversity, Equity, and Inclusion: ,

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Keyskills:   CAPA Vendor Qualification