Technical Staff
PharmaClinical ResearchRegulatory AffairsQuality Assurancegmpcdmcrosap
Job description
Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : www.piramalpharmasolutions.com Job Title Technical Staff Job Description Responsible for proper receipt and storage of Finished goods materials as per cGMP norms. Responsible for data entry in S4 HANA (SAP) & eWMS system. Responsible for compliance of regulatory requirements as per cGMP norms. Responsible for receipt storage and handling of Finished Goods materials.. Timely complete the preppartory work of Palletization and retrival of FG goods for dispatch. Responsible for correct data entry and handling of WMS program in SAP system. Responsible for maintaining routine housekeeping in warehouse areas as per cGMP norms. Responsible for disposal of rejected/Expiredand Write-off materials and its documentation. Responsible for coordinate with Planning/Purchase/QC/Production for smooth operation. Responsible for collect / deposit of cGMP documents and arrangement for submitting the same to QA department after completion. Responsible for handling, maintenance, verification and calibration of equipment’s/instruments in warehouse. Responsible for timely attend the trainings on cGMP documents and revised documents. Responsible to ensure EHS (Environmental, Health and Safety) related activities to be completed on time and to support EHS activities as per the requirements. To ensure data integrity compliances at site and while performing activities. Responsible for monitoring and maintenance of safety compliance at work place. Responsible to maintain good hygiene, safety practices and cGMP practices.
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