Walk-in Drive For Officer / Executive - Injectable Manufacturing

Intas · Bavla

  • Experience4–9 yrs
  • SalaryNot disclosed
  • Work modeonsite
  • Posted26 Sept 2026
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About Intas

Intas is hiring in Bavla in pharma biotech. This role looks for around 4+ years of experience.

Skills

  • aseptic filling
  • sterile compounding
  • lyophilization
  • cGMP
  • USFDA
  • EMA
  • MHRA
  • line validation
  • equipment qualification
  • media fills
  • data integrity
  • root-cause analysis
  • CAPA
  • environmental monitoring
  • material reconciliation

The role

A pharmaceutical manufacturing production officer at a sterile injectable company supervises aseptic filling, lyophilization, and cGMP compliance while managing validation and CAPA. The role also oversees environmental monitoring and equipment troubleshooting across cleanroom operations.

Full job description

Role & responsibilities: -

Production Supervision: Supervise daily operations across sterile compounding, aseptic filtration, filling, sealing, and lyophilization (freeze-drying) lines for ampoules and vials.

Equipment Troubleshooting: Operate, calibrate, and troubleshoot critical machinery including vial washing systems, depyrogenation tunnels, autoclaves, and high-speed filling lines.

cGMP & Audit Compliance: Ensure strict adherence to current Good Manufacturing Practices (cGMP) and actively participate in regulatory audits like USFDA, EMA, and MHRA.

Validation & Media Fills: Lead and document line validation activities, equipment qualifications, and routine media fill trials to ensure cleanroom sterility.

Documentation Review: Author and review Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and line logs in real-time, enforcing strict data integrity.

Deviation & CAPA Management: Investigate shop-floor deviations, conduct root-cause analysis (RCA), and implement effective Corrective and Preventive Actions (CAPA).

Environmental Monitoring: Oversee Grade A/B/C/D cleanroom parameters, including differential pressure, viable/non-viable particle counts, temperature, and humidity.

Material Reconciliation: Manage the dispensing of raw materials and execute precise product reconciliation at every stage of the manufacturing cycle.

Team Leadership: Lead and train a shift team of junior officers, technicians, and operators to maintain optimum line efficiency and safety.

Cross-Functional Coordination: Collaborate daily with Quality Assurance (QA), Quality Control (QC), Engineering, and Warehouse teams to ensure smooth batch releases.

Preferred candidate profile: -

Required Experience: - 3 to 10 Years

Required Educational Qualification: - M.Pharm. / B. Pharm.

Regards,

Human Resources Department,

Intas Pharmaceuticals SEZ Plant