? Key Responsibilities:
- Execute day-to-day operations in aseptic and sterile manufacturing areas
- Monitor LVP production activities in compliance with SOPs, cGMP, and regulatory guidelines
- Operate and maintain critical equipment including autoclaves, filling machines, and sterilizers
- Ensure strict adherence to safety, quality, and environmental standards
- Prepare, review, and maintain batch production records and related documentation
? Qualifications & Skills:
- Bachelor’s degree in Pharmacy, Chemistry, or Life Sciences
- 1–5 years of experience in sterile pharmaceutical manufacturing (LVP experience preferred)
- Strong knowledge of aseptic techniques, cleanroom behavior, and validation processes
- Valuable documentation practices and regulatory awareness
📌 Production Chemist Officer/Executive for LVP company (Kadi)
🏢 Pramukh Staffing
📍 Kadi
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