Pharmaceutical Quality Assurance Executive Graduate Experience Jobs in Nashik

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Opening For Quality Assurance Executive

Impact HR & KM Solutions

  • 2 - 3 yrs
  • 3.0 Lac/Yr
  • Nashik
QA-quality Assurance Quality Assurance Executive Executive Quality Assurance Pharmaceutical Quality Assurance Executive Executive Corporate Quality Assurance
Key ResponsibilitiesShop Floor & IPQA OperationsPerform line clearance for dispensing, manufacturing, filling, and packaging operations.Execute In-Process Quality Assurance (IPQA) checks during production and ensure strict compliance with Master Batch Records (BMR/BPR).Monitor ambient environmental parameters, cleanroom conditions, differential pressure, and water system sampling.Quality Management System (QMS)Handle QMS elements including Deviations, Change Controls, Corrective and Preventive Actions (CAPA), and Out of Specification (OOS) investigations.Conduct root cause analysis (RCA) using tools like 5 Whys and Fishbone diagrams for quality incidents.Coordinate internal audits, self-inspections, and follow up on audit observations to closure.Documentation & Batch ReleaseReview executed Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) prior to final batch release.Draft, review, and periodically update Standard Operating Procedures (SOPs), Validation Protocols, and Qualification Reports.Prepare Annual Product Quality Reviews (APQR/PQR) and trend reports for Critical Quality Attributes (CQAs).
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QA Executive - Pharma (2-8 Years)

Impact HR & KM Solutions

  • 2 - 8 yrs
  • 6.0 Lac/Yr
  • Nashik
QA-quality Assurance Quality Assurance Executive Executive Quality Assurance Pharmaceutical Quality Assurance Executive
Key Responsibilities:Ensure implementation and compliance with cGMP, GLP, GDP, and regulatory guidelines (WHO, USFDA, EU-GMP, Schedule M).Review and approve Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), SOPs, specifications, and protocols.Handle deviations, change controls, OOS/OOT investigations, CAPA, and risk assessments.Monitor in-process quality checks and finished product documentation.Participate in internal, external, and regulatory audits and ensure timely closure of audit observations.Perform and review validation activities including process validation, cleaning validation, and equipment qualification.Control and maintain QA documentation, logs, and quality records.Coordinate with Production, QC, Engineering, and Warehouse teams for quality-related activities.Support product release and market complaint handling.Ensure compliance with data integrity and documentation practices.Required Qualifications:B.Pharm / M.Pharm / B.Sc / M.Sc (Chemistry or related discipline)1-5 years of experience in Quality Assurance within a pharmaceutical manufacturing environmentStrong knowledge of GMP documentation and regulatory compliancePreferred Skills & Competencies:Hands-on experience with regulatory audits (WHO / USFDA / MHRA)Knowledge of pharmaceutical quality systems (QMS)Good understanding of validation and qualification proceduresStrong analytical, documentation, and problem-solving skillsProficiency in MS Office and quality management systemsGood communication and coordination abilitiesIndustry:Pharmaceuticals / API / Formulations
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