To oversee and ensure smooth production activities in the pharmaceutical manufacturing unit as per cGMP, SOPs, and regulatory guidelines while maintaining quality, safety, and efficiency standards.
Key Responsibilities:
Execute day-to-day production activities as per approved batch manufacturing records (BMR) and standard operating procedures (SOPs).
Monitor and control manufacturing processes, ensuring adherence to cGMP, GDP, and safety norms.
Handle equipment operation, cleaning, and calibration related to the production process.
Maintain proper documentation of production activities, including BMRs, logbooks, and deviation reports.
Coordinate with QA/QC teams for in-process checks, validations, and compliance requirements.
Ensure optimum utilization of manpower, machinery, and material to achieve production targets.
Identify and troubleshoot process deviations or equipment malfunctions.
Participate in audits (internal/external) and regulatory inspections.
Train operators and workers on GMP practices, hygiene, and safe handling of materials.
Support scale-up, technology transfer, and process improvements in production.
Qualifications & Experience:
B.Sc. / M.Sc. in Chemistry / Industrial Chemistry / Pharmaceutical Sciences.
2-5 years of experience in a pharmaceutical manufacturing unit (formulations / bulk drugs / API, as applicable).
Sound knowledge of cGMP, regulatory guidelines (USFDA, WHO, GMP), and production processes.
Experience in handling manufacturing equipment and documentation.
Skills & Competencies:
Strong technical and analytical skills.
Good knowledge of pharmaceutical production processes.
Attention to detail and documentation accuracy.
Teamwork, coordination, and problem-solving skills.
Ability to work under pressure and meet deadlines.
Job Types: Full-time, Permanent
Pay: ₹25,000.00 - ₹35,000.00 per month
Benefits:
Health insurance
Provident Fund
Experience:
Pharmaceutical OSD production : 3 years (Required)
Work Location: In person
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