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.

Pay: From ₹15,000.00 per month

**Benefits**:

- Leave encashment

Schedule:

- Day shift

Supplemental Pay:

- Yearly bonus

Work Location: In person