. The role involves supervising daily operations, ensuring GMP compliance, managing manpower, and maintaining production records. Candidates must have a pharmaceutical background and hands-on experience in solid dosage and liquid formulations.
Key Responsibilities:
Supervise and manage production of capsules, and tablets
Ensure adherence to GMP, SOPs, and safety standards
Coordinate with QA/QC and other departments for smooth operations
Maintain daily production reports and batch records
Monitor machinery and coordinate preventive maintenance
Train and guide production staff for efficiency and compliance
Qualifications:
B.Pharm or M.Pharm
(mandatory)
Minimum 2-3 years of experience in solid dosage and liquid formulation section
Strong understanding of pharmaceutical manufacturing processes
Good communication and team management skills
Job Type: Full-time
Benefits:
Provident Fund
Education:
Bachelor's (Required)
Work Location: In person
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