Production Officer pharma

SAIN MEDICAMENTS PVT. LTD; Uppal; On-site; INR 400,000 - 800,000; Full time

Job summary

SAIN MEDICAMENTS PVT. LTD is seeking a dedicated Production Officer to oversee daily manufacturing in a GMP-compliant pharmaceutical facility in Telangana. The ideal candidate will have a B.Pharm or M.Pharm and 2–5 years of experience in pharmaceutical production. Responsibilities include executing production plans, ensuring quality compliance, and maintaining documentation. The role requires strong monitoring skills and team supervision. Join us for a fulfilling career in a dynamic industry.

Qualifications

• Bachelor's or Master's degree in Pharmacy or related fields.
• 2–5 years of experience in pharmaceutical production.
• Good documentation and communication skills.

Responsibilities

• Execute and monitor production activities as per approved BMR and SOPs.
• Ensure timely completion of batches as per production schedule.
• Supervise operators and ensure proper utilization of manpower.
• Maintain BMR, logbooks, and other production records accurately.
• Ensure adherence to GMP, safety, and hygiene standards.
• Perform line clearance before and after batch operations.

Skills

Pharmaceutical Production

GMP / SOP Compliance

BMR Documentation

Process Monitoring

Team Supervision

Deviation Handling

Education

B.Pharm / M.Pharm / B.Sc / M.Sc (Chemistry / Life Sciences)

Job description

Job Title: Production Officer

Industry: Pharmaceuticals (Formulation)

Department: Production

We are looking for a responsible Production Officer to oversee day-to-day manufacturing activities in a GMP-compliant pharmaceutical facility. The role involves executing production plans, ensuring quality compliance, maintaining documentation, and coordinating with cross-functional teams to meet production targets.

Key Responsibilities

• Execute and monitor production activities as per approved Batch Manufacturing Records (BMR) and SOPs
• Ensure timely completion of batches as per production schedule
• Supervise operators and ensure proper utilization of manpower
• Maintain and review BMR, logbooks, and other production records accurately
• Ensure adherence to GMP, safety, and hygiene standards in the production area
• Perform line clearance before and after batch operations
• Coordinate with QA/QC for in-process checks, sampling, and approvals
• Monitor critical process parameters and ensure product quality
• Report and assist in handling deviations, incidents, and non-conformances
• Ensure proper cleaning and maintenance of equipment as per SOPs
• Support validation, qualification, and technology transfer activities

GMP & Compliance Responsibilities

• Follow GMP guidelines and data integrity practices (ALCOA+)
• Ensure audit readiness at all times
• Participate in internal, external, and regulatory audits
• Maintain proper documentation as per regulatory requirements

Key Skills

• Pharmaceutical Production
• GMP / SOP Compliance
• BMR Documentation
• Process Monitoring
• Team Supervision
• Deviation Handling

Eligibility Criteria

• Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc (Chemistry / Life Sciences)
• Experience: 2–5 years in pharmaceutical production

Preferred Candidate Profile

• Experience in formulation/API manufacturing units
• Exposure to regulatory audits (USFDA, WHO, etc.)
• Good documentation and communication skills