Production Officer / Executive – Pharmaceutical Manufacturing (Topicals)

About the RoleWe are hiring production professionals with hands-on experience manufacturing creams, ointments, gels, or lotions in a cGMP pharmaceutical facility. We operate under cGMP standards and are looking for a hands-on, detail-oriented production professional to join our manufacturing team at our Bavla facility.This role is open across levels — Production Officer, Production Executive, and Sr. Executive — and will be matched to the right candidate based on experience and capability. If you have 2 to 6 years of experience in pharmaceutical production and thrive in a disciplined, process-driven manufacturing environment, we'd like to hear from you.You will report to the Production Manager / Production Head and work closely with QA, QC, Stores, and Engineering to keep operations running smoothly and compliantly.QualificationsB.Pharm, M.Pharm, B.Sc (Chemistry / Microbiology / Life Sciences), or M.Sc in a relevant discipline2 to 6 years of experience in pharmaceutical manufacturing — specifically in topical / semi-solid / liquid dosage forms preferredWorking knowledge of cGMP, GDP, and SOPs as applied in a regulated manufacturing environmentCandidates must have prior experience in a pharmaceutical manufacturing facility.Key Responsibilities:Production ExecutionExecute the approved monthly production plan in line with cGMP requirements and facility SOPsCarry out manufacturing and packing operations strictly per approved BMR/BPR and validated process parametersPerform and document line clearance before batch start and after batch completionDocumentation & ComplianceMaintain real-time, accurate entries in BMR/BPR records and area logbooksFollow Good Documentation Practices (GDP) and data integrity principles at all timesAssist in the preparation and periodic review of BMR/BPR documentsMaterial & Process ControlEnsure correct status labeling and segregation of raw, packing, and in-process materials.Verify material receipt, issuance, storage, and batch-wise reconciliationMonitor in-process control parameters and ensure results remain within specified limitsEquipment & Area ManagementOperate, clean, and maintain equipment in accordance with applicable SOPsEnsure proper handling, storage, and accountability of machine change partsMaintain manufacturing areas to cGMP, EHS, and hygiene standards at all timesDeviation & Quality SystemsPromptly report deviations, equipment breakdowns, or process abnormalities to the appropriate teamsSupport root cause investigations and assist in implementing CAPAsCross-Functional CoordinationCoordinate with QA, Stores, Engineering, and HR to ensure uninterrupted, compliant production operationsContinuous ImprovementParticipate actively in training programs and competency assessmentsSupport process validation activities, equipment qualification, and internal or external auditsPreferred ExperienceHands-on experience in manufacturing of creams, ointments, gels, or lotions in a cGMP-compliant facilityFamiliarity with BMR/BPR documentation, in-process controls, and batch reconciliationExposure to deviation management, CAPA processes, or internal audit supportExperience working cross-functionally with QA and Stores in a production setting

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