Job Summary

We are looking for an experienced Pharma Production In-Charge to supervise and manage day-to-day pharmaceutical production activities. The candidate will be responsible for achieving production targets while ensuring compliance with GMP, SOPs, quality standards, safety requirements, and regulatory guidelines.

Key Responsibilities

- Plan, coordinate, and supervise daily pharmaceutical production activities.

- Ensure production is carried out as per approved Batch Manufacturing Records (BMR) and SOPs.

- Ensure adherence to GMP, GLP, safety, and hygiene requirements applicable to the facility.

- Monitor batch manufacturing activities from dispensing to processing, filling, packing, and finished-product transfer, as applicable.

- Ensure proper line clearance before starting production activities.

- Verify availability and status of raw materials, packaging materials, equipment, and manpower.

- Coordinate with QA/QC, Warehouse, Engineering, Purchase, and Maintenance departments.

- Ensure accurate and timely completion of batch records, logbooks, checklists, and production reports.

- Monitor critical process parameters and ensure they remain within approved limits.

- Investigate and report production deviations, incidents, breakdowns, and process abnormalities.

- Coordinate with QA for deviation, CAPA, change control, and other quality-related activities.

- Ensure proper identification, handling, storage, and traceability of raw materials and finished products.

- Monitor production yields, material reconciliation, wastage, rejection, and productivity.

- Ensure proper cleaning and sanitation of production areas and equipment.





- Ensure equipment is operated and maintained according to approved procedures.

- Supervise and train production staff on GMP, SOPs, safety, hygiene, and production procedures.

- Monitor staff attendance, shift allocation, discipline, and productivity.

- Ensure compliance with safety procedures and report unsafe conditions immediately.

- Prepare daily, weekly, and monthly production reports for management.

- Identify process bottlenecks and implement improvements to enhance productivity and reduce wastage.

- Support internal, customer, and regulatory audits and ensure timely closure of observations.

- Ensure all production activities are carried out in accordance with applicable pharmaceutical regulatory requirements.

Required Qualifications

- B.Pharm / M.Pharm / B.Sc / M.Sc / Diploma in Pharmacy or relevant pharmaceutical/technical qualification.

- 3–8 years of experience in pharmaceutical manufacturing/production.

- Experience in handling production teams and pharmaceutical manufacturing operations.

- Hands-on knowledge of GMP, SOPs, BMR/BPR, batch documentation, and production processes.

Required Skills

- Strong knowledge of pharmaceutical production processes.

- Good understanding of GMP and documentation practices.

- Knowledge of BMR/BPR and batch reconciliation.

- Good understanding of deviation, CAPA, change control, and incident reporting.

- Strong leadership and team-management skills.

- Positive problem-solving and decision-making ability.

- Good communication and interdepartmental coordination skills.

- Good knowledge of MS Excel and production reporting.

- Strong attention to detail and documentation accuracy.

Benefits

- Flexible schedule

- Provident Fund

Work Location: In person

📌 Production Incharge (Pharma) (Madurai)
🏢 Wedjat Health Solutions Private Limited, Madurai
📍 Madurai