Job Description

About the Role

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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.

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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.

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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.

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Qualifications

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- B.Pharm, M.Pharm, B.Sc (Chemistry / Microbiology / Life Sciences), or M.Sc in a relevant discipline
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- 2 to 6 years of experience in pharmaceutical manufacturing — specifically in topical / semi-solid / liquid dosage forms preferred
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- Working knowledge of cGMP, GDP, and SOPs as applied in a regulated manufacturing environment
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- Candidates must have prior experience in a pharmaceutical manufacturing facility.
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Key Responsibilities:

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Production Execution

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- Execute the approved monthly production plan in line with cGMP requirements and facility SOPs
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- Carry out manufacturing and packing operations strictly per approved BMR/BPR and validated process parameters
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- Perform and document line clearance before batch start and after batch completion
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Documentation & Compliance

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- Maintain real-time,



accurate entries in BMR/BPR records and area logbooks
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- Follow Good Documentation Practices (GDP) and data integrity principles at all times
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- Assist in the preparation and periodic review of BMR/BPR documents
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Material & Process Control

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- Ensure correct status labeling and segregation of raw, packing, and in-process materials.
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- Verify material receipt, issuance, storage, and batch-wise reconciliation
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- Monitor in-process control parameters and ensure results remain within specified limits
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Equipment & Area Management

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- Operate, clean, and maintain equipment in accordance with applicable SOPs
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- Ensure proper handling, storage, and accountability of machine change parts
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- Maintain manufacturing areas to cGMP, EHS, and hygiene standards at all times
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Deviation & Quality Systems

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- Promptly report deviations, equipment breakdowns, or process abnormalities to the appropriate teams
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- Support root cause investigations and assist in implementing CAPAs
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Cross-Functional Coordination

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- Coordinate with QA, Stores, Engineering, and HR to ensure uninterrupted, compliant production operations
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Continuous Improvement

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- Participate actively in training programs and competency assessments
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- Support process validation activities, equipment qualification, and internal or external audits
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Preferred Experience

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- Hands-on experience in manufacturing of creams, ointments, gels, or lotions in a cGMP-compliant facility
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- Familiarity with BMR/BPR documentation, in-process controls, and batch reconciliation
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- Exposure to deviation management, CAPA processes, or internal audit support
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- 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