▷ [30/10/2025] Executive - Quality Assurance

Area and line clearance for Manufacturing Packing Dispensing activity in production area In process checks in Manufacturing and Packing activity Daily verification of weighing balance calibration activity Daily verification of environmental monitoring of raw material staging area and Manufacturing and Packing area Verification of each equipment cleanliness and area cleanliness during line clearance Verification and review of online Batch Manufacturing Records Issuance of BMR BPR logbooks formats Re-issuance of additional page requirement of BMR BPR on requisition by production Sampling of bulk stage finished goods analysis and control sample Verification of production documents Daily nonconformance observation reported and maintained In process quality checks in Tablet Liquid HNH ANH manufacturing dept Line Clearance for Manufacturing Packing Dispensing activity Sampling of validation sample Process packaging cleaning rinse swab samples Review of production records and Finished Goods verification On job training to the new people working in the production area Statistical Process Monitoring Online observation of process deviation and effective implementation of CAPA Reporting of daily nonconformance Execution of requirements for food Dietary supplements regulations for export market US -21 CFR Part 111 Ensuring avoidance of breach of data integrity in area Implementation of effective sanitation program in area Imparting required training to shop floor personnel Adherence to the requirements of EHS norms Execution of various initiatives as are suggested by corporate functions SEEDS Learning university Quality mindset Customer centricity Document Archival To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same To implement QEHS policy objectives To ensure participation and consultation of worker Ensure use of PPE To identify communicate incidents QEHS nonconformities investigate and take corrective actions on the same To ensure work permit system during maintenance activities To implement QEHS continual improvement projects at site and monitor To ensure disposal of waste Authorised to prevent improper workplace conditions Authorised for reporting of Hazards Incident Accidents and Near miss reporting Authorised to prepare OH S performance document Authorised to conduct training of workmen s related to OHSMS In the three decades of its existence Piramal Group has pursued a twin strategy of both organic and inorganic growth Driven by its core values Piramal Group steadfastly pursues inclusive growth while adhering to ethical and values-driven practices Equal employment opportunityPiramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer We do not discriminate based upon race ethnicity religion color national origin gender including pregnancy childbirth or related medical conditions sexual orientation gender identity gender expression age status as a protected veteran status as an individual with a disability genetics or other applicable legally protected characteristics We base our employment decisions on merit considering qualifications skills performance and achievements We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters including recruitment selection training placement promotion demotion compensation and benefits transfers terminations and working conditions including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice Piramal Pharma Solutions PPS is a Contract Development and Manufacturing Organization CDMO offering end-to-end development and manufacturing solutions across the drug life cycle We serve our customers 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 such as the development and manufacture of highly potent APIs antibody-drug conjugations sterile fill finish peptide products services and potent solid oral drug products PPS also offers development and manufacturing services for biologics including vaccines gene therapies and monoclonal antibodies made possible through Piramal Pharma Limited s investment in Yapan Bio Private Limited Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide