Production - External preparation

Umendra Life Sciences Pvt. Ltd.; Ahmedabad District; On-site; INR 420,000 - 640,000; Full time

Job summary

Umendra Life Sciences Pvt. Ltd. in Bavla (Gujarat) is seeking production professionals with hands-on experience manufacturing creams, ointments, gels, or lotions in a cGMP pharmaceutical facility.

You will report to the Production Manager and collaborate with QA, QC, Stores, and Engineering to keep operations compliant. Open across levels — Production Officer, Production Executive, and Sr. Executive — with 2–6 years of pharma production, you thrive in a disciplined, process-driven environment

Qualifications

• B.Pharm, M.Pharm, B.Sc (Chemistry / Microbiology / Life Sciences) or M.Sc with 2–6 years pharma production.
• Experience in topical / semi-solid / liquid dosage forms preferred.
• Prior experience in a pharmaceutical manufacturing facility with cGMP, GDP and SOPs.

Responsibilities

• Execute the approved monthly production plan per cGMP requirements and SOPs.
• Document line clearances and maintain accurate BMR/BPR records.
• Verify material receipt, issuance, storage and batch reconciliation.
• Operate, clean and maintain equipment according to SOPs.
• Support deviations, CAPA investigations and data integrity practices.
• Coordinate with QA, Stores, Engineering and HR for compliant operations.
• Contribute to training and cross-functional improvement activities.

Skills

Production experience

cGMP knowledge

Documentation discipline

Education

B.Pharm, M.Pharm, B.Sc (Chemistry / Microbiology / Life Sciences), or M.Sc

Job description

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 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.

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
• 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