Quality Assurance Executive

6 days ago


Hyderabad, India Rashmi Pharma Pvt. Ltd. Full time

1. QA Executive – Junior LevelExperience Required: 2–4 yearsSalary Offered: ₹20,000 per monthJob Summary:We are seeking motivated QA Executives with 2–4 years of experience to support daily quality assurance activities in a GMP-regulated pharmaceutical facility. The role will focus on documentation review, QA activities, and ensuring compliance with regulatory standards.Key Responsibilities:Review batch manufacturing and packing recordsLine clearance for production and packaging activitiesSupport in handling deviations, change controls, CAPA, and incident reportsEnsure compliance with cGMP and Revised Schedule M requirementsParticipate in in-process checks and quality monitoringAssist in preparation and review of SOPs, logbooks, and other controlled documentsSupport internal audits and regulatory inspection readinessQualifications:B.Pharm / M.Pharm / B.Sc / M.Sc (Life Sciences/Chemistry)2–4 years of experience in QA in a pharmaceutical companyGood understanding of cGMP and QMS principlesStrong documentation and communication skills2. QA Executive – Mid-LevelExperience Required: 4–8 yearsSalary Offered: ₹30,000 per monthJob Summary:We are looking for experienced QA Executives with 4–8 years of experience to take responsibility for advanced QA functions, including compliance management, documentation oversight, and training of junior QA staff.Key Responsibilities:Review and approval of batch records, logbooks, and controlled documentsOversee line clearance, in-process checks, and QA complianceLead and investigate deviations, OOS, OOT, change controls, and CAPACoordinate with production, QC, and engineering for quality complianceHandle document control, issuance, archival, and retrieval systemsSupport vendor qualification and raw material quality compliancePrepare for and participate in internal audits and regulatory inspectionsMentor and guide junior QA team membersQualifications:B.Pharm / M.Pharm / B.Sc / M.Sc (Life Sciences/Chemistry)4–8 years of QA experience in a pharmaceutical manufacturing unitStrong knowledge of QMS, regulatory compliance, and cGMPExperience in facing audits (USFDA/WHO/other regulatory bodies is an advantage)Excellent analytical, communication, and leadership skills



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