Sun Pharma Hiring for Quality Assurance Jobs | Opening for B.Pharm & M.Pharm
Looking for a Quality Assurance Job in the pharmaceutical industry? Sun Pharma Careers brings an excellent opportunity for B.Pharm and M.Pharm professionals with 2+ years of experience to join one of India’s leading pharmaceutical companies. This Quality Assurance Job at Halol offers hands-on exposure to GMP compliance, production operations, documentation, validation, and quality systems while helping you build a rewarding career through Sun Pharma Careers.
- Job Title: Executive
- Job Grade: G12A
- Location: Halol 2
About the Company
Sun Pharmaceutical Industries Ltd. is one of the world’s largest specialty generic pharmaceutical companies, delivering high-quality, affordable medicines across numerous therapeutic segments. Through innovation, operational excellence, and a strong commitment to quality, Sun Pharma continues to create rewarding career opportunities for pharmaceutical professionals worldwide.
Key Responsibilities
- Authorized to sign cGMP documents including equipment logs, temperature & RH records, cleaning records, calibration records, and in-process approvals.
- Maintain Batch Manufacturing Records (BMR), test requisitions, and bulk quarantine/staging records.
- Manage day-to-day production activities in the Tablet (FBE) department ensuring quality, quantity, and GMP compliance.
- Support smooth manufacturing operations and assist other officers in production control.
- Ensure all processes follow GMP guidelines and update procedures when required.
- Coordinate with QA and QC teams for validation and product quality compliance.
- Conduct GMP training for staff and operators across departments.
- Optimize usage of manpower, materials, and machines for better efficiency.
- Prepare daily production and departmental activity reports.
- Handle calibration, qualification, and validation of equipment and processes.
- Manage procurement of machinery, spare parts, and required materials.
- Prepare and execute destruction notes as per procedure.
- Maintain all GMP documentation including logbooks, monitoring records, and housekeeping logs.
- Train and guide team members to ensure GMP compliance and standardized work practices.
- Take responsibility for the Officer role in the absence of the senior officer.
- Coordinate with Warehouse, MIS, and Engineering for material planning and preventive maintenance.
- Prepare and revise BMR, SOPs, and Protocols for new products and equipment.
Qualification
- B.Pharm / M.Pharm
- Experience: 2+ years
