Job Description About the Role
n We 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.
n 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 setting, we'd like to hear from you.
n 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.
n Qualifications
n n B.Pharm, M.Pharm, B.Sc (Chemistry / Microbiology / Life Sciences), or M.Sc in a relevant discipline
n 2 to 6 years of experience in pharmaceutical manufacturing — specifically in topical / semi-solid / liquid dosage forms preferred
n Working knowledge of cGMP, GDP, and SOPs as applied in a regulated manufacturing environment
n Candidates must have prior experience in a pharmaceutical manufacturing facility.
n n Key Responsibilities:
n Production Execution
n n Execute the approved monthly production plan in line with cGMP requirements and facility SOPs
n Carry out manufacturing and packing operations strictly per approved BMR/BPR and validated process parameters
n Perform and document line clearance before batch start and after batch completion
n n Documentation & Compliance
n n Maintain real-time,



accurate entries in BMR/BPR records and area logbooks
n Follow Good Documentation Practices (GDP) and data integrity principles at all times
n Assist in the preparation and periodic review of BMR/BPR documents
n n Material & Process Control
n n Ensure correct status labeling and segregation of raw, packing, and in-process materials.
n Verify material receipt, issuance, storage, and batch-wise reconciliation
n Monitor in-process control parameters and ensure results remain within specified limits
n n Equipment & Area Management
n n Operate, clean, and maintain equipment in accordance with applicable SOPs
n Ensure proper handling, storage, and accountability of machine change parts
n Maintain manufacturing areas to cGMP, EHS, and hygiene standards at all times
n n Deviation & Quality Systems
n n Promptly report deviations, equipment breakdowns, or process abnormalities to the appropriate teams
n Support root cause investigations and assist in implementing CAPAs
n n Cross-Functional Coordination
n n Coordinate with QA, Stores, Engineering, and HR to ensure uninterrupted, compliant production operations
n n Continuous Improvement
n n Participate actively in training programs and competency assessments
n Support process validation activities, equipment qualification, and internal or external audits
n n Preferred Experience
n n Hands-on experience in manufacturing of creams, ointments, gels, or lotions in a cGMP-compliant facility
n Familiarity with BMR/BPR documentation, in-process controls, and batch reconciliation
n Exposure to deviation management, CAPA processes, or internal audit support
n Experience working cross-functionally with QA and Stores in a production setting
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📌 Production - Pharmaceutical Manufacturing (External preparation) (Ahmedabad)
🏢 Umendra Life Sciences
📍 Ahmedabad