QA Chemist

Production Planning & Execution:

· Execute daily production activities on the shop floor as per the approved production schedule.

· Plan and allocate manpower shifts and distribute work effectively with proper supervision.

· Allocate and monitor utilities to meet production schedules and ensure continuous functionality.

Coordination with Departments:

· Liaise with Warehouse/Stores/Procurement for timely availability of raw materials to meet production targets.

· Coordinate with the QC Department for timely analysis, approval, or rejection of in-process samples, intermediate, and finished products to maintain quality standards.

· Work closely with the QA Department to ensure compliance with GMP and ISO requirements, and adherence to all quality management procedures.

Line Clearance & Process Verification:

· Ensure proper line clearance before initiation of manufacturing and packaging activities.

· Monitor critical steps during manufacturing and packaging to ensure product quality and consistency.

Batch Manufacturing:

· Execute and supervise daily production activities including granulation, compression, coating, filling, and packaging.

· Ensure timely completion of batch manufacturing records (BMRs).

Documentation & Record Keeping:

· Maintain accurate documentation, including Batch Manufacturing Records (BMR), Log Books, Calibration Records, and other relevant documents in compliance with GMP and ISO standards.

· Ensure good housekeeping practices in production areas, equipment, utility zones, and the factory premises.

· Maintain accurate and timely documentation for all IPQA activities.

Equipment Maintenance & Troubleshooting:

· Oversee calibration and maintenance of machines.

· Manage installation, training, and maintenance of new equipment.

· Address troubleshooting issues promptly and effectively.

· Develop and maintain packaging materials (primary, secondary, tertiary) and pallet preparation materials.

Deviation & Incident Handling:

· Report and assist in the investigation of deviations, incidents, and out-of-specification (OOS) results.

Sampling Activities:

· Perform sampling of raw materials, in-process materials, and finished products as per SOPs.

SOP Adherence & Compliance Monitoring:

· Participate in training programs and ensure all activities follow current SOPs and quality policies.

· Ensure operations are carried out in compliance with GMP, SOPs, and regulatory guidelines.

Batch Record Review:

· Review and verify batch manufacturing records (BMRs) and batch packaging records (BPRs) during execution

GMP Audits and Inspection Readiness:

· Support internal and external audits by ensuring GMP compliance and documentation accuracy.

Quality Management & Continuous Improvement:

· Review BMR, Batch Packing Records (BPR), Master Formula Records, and Master Packing Records.

· Prepare and review Change Controls, Deviations, CAPA, Site Master Files, Validation Protocols, and Dossiers in alignment with the latest Quality Management System (QMS) guidelines.

· Prepare Standard Operating Procedures (SOPs) for manufacturing and packaging areas.

· Implement Corrective and Preventive Actions (CAPA) on the shop floor.

· Ensure timely delivery of products as per the production plan.

Training & Development:

· Conduct on-the-job training for production staff on shop floor activities, GMP, and SOPs.

· Support manpower development in areas of quality, productivity, and cost efficiency.

Job Types: Full-time, Permanent

Pay: ₹15, ₹20,000.00 per month

Benefits:

• Cell phone reimbursement

Work Location: In person