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21 hours ago
Interested candidates are requested to share their resumes at for interview scheduling on 7th September 2025 at Hotel Ginger, Bharuch. Please note that it is mandatory to pre-schedule the interview before reporting at the venue.
Responsibilities:
- Carry out routine production activities for Small Volume Parenterals (SVP) in compliance with cGMP and SOPs.
- Operate and monitor aseptic filling, sterilization, and packaging equipment.
- Ensure accuracy and completeness of Batch Manufacturing Records (BMR) and other production documentation.
- Adhere to cleanroom and aseptic practices during SVP manufacturing.
- Coordinate with QA, QC, and Engineering for smooth batch execution.
- Support in deviation handling, investigations, and CAPA.
- Maintain EHS and data integrity standards in day-to-day operations.
Requirements:
- B.Pharm / M.Pharm / B.Sc. with 2 to 5 years of experience in SVP production.
- Hands-on experience in aseptic filling, sterilization, and cleanroom operations.
- Knowledge of regulatory guidelines (USFDA, MHRA, WHO, etc.).
- Strong compliance and documentation skills.
Key Skills: SVP Manufacturing, Aseptic Processing, Sterile Operations, cGMP Compliance, Documentation.
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