About the Role 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. 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. 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.

Qualifications

B.Pharm, M.Pharm, B.Sc (Chemistry / Microbiology / Life Sciences), or M.Sc in a relevant discipline

2 to 6 years of experience in pharmaceutical manufacturing — specifically in topical / semi-solid / liquid dosage forms preferred

Working knowledge of cGMP, GDP, and SOPs as applied in a regulated manufacturing environment

Candidates must have prior experience in a pharmaceutical manufacturing facility.

Key Responsibilities: Production Execution

Execute the approved monthly production plan in line with cGMP requirements and facility SOPs

Carry out manufacturing and packing operations strictly per approved BMR/BPR and validated process parameters

Perform and document line clearance before batch start and after batch completion Documentation & Compliance

Maintain real-time,



accurate entries in BMR/BPR records and area logbooks

Follow Good Documentation Practices (GDP) and data integrity principles at all times

Assist in the preparation and periodic review of BMR/BPR documents Material & Process Control

Ensure correct status labeling and segregation of raw, packing, and in-process materials.

Verify material receipt, issuance, storage, and batch-wise reconciliation

Monitor in-process control parameters and ensure results remain within specified limits Equipment & Area Management

Operate, clean, and maintain equipment in accordance with applicable SOPs

Ensure proper handling, storage, and accountability of machine change parts

Maintain manufacturing areas to cGMP, EHS, and hygiene standards at all times Deviation & Quality Systems

Promptly report deviations, equipment breakdowns, or process abnormalities to the appropriate teams

Support root cause investigations and assist in implementing CAPAs Cross-Functional Coordination

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

Participate actively in training programs and competency assessments

Support process validation activities, equipment qualification, and internal or external audits Preferred Experience

Hands-on experience in manufacturing of creams, ointments, gels, or lotions in a cGMP-compliant facility

Familiarity with BMR/BPR documentation, in-process controls, and batch reconciliation

Exposure to deviation management, CAPA processes, or internal audit support

Experience working cross-functionally with QA and Stores in a production setting

📌 Production - Pharmaceutical Manufacturing (External preparation) (Ahmedabad)
🏢 Umendra Life Sciences
📍 Ahmedabad