Qualification: M.Pharma / B.Pharma / M.Sc (Microbiology/Biotechnology)
Experience: 1–4 years (preferably in aseptic/sterile manufacturing)
Shift: Rotational/Day Shift
Job Description:
- Supervise and monitor aseptic manufacturing operations in sterile injectable plant
- Ensure compliance with GMP, CDC, and contamination control protocols
- Oversee critical processes: compounding, filling, stoppering, and sealing
- Maintain Batch Manufacturing Records (BMR), logbooks, and documentation
- Monitor environmental conditions (temperature, pressure, particle count)
- Coordinate with QA/QC departments for quality checks and approvals
- Train junior staff on aseptic techniques and SOPs
- Report deviations and participate in investigations
Requirements:
- Strong knowledge of sterile manufacturing and aseptic techniques
- Understanding of HVAC, laminar flow, and cleanroom operations
- Good analytical and problem-solving skills
- Ability to work under pressure and meet production targets
Work Location: In person
