Overall Responsibilities
- Production Planning: Develop and implement production plans and schedules, ensuring timely delivery and cost-effective manufacturing.
- Process Supervision: Oversee batch manufacturing, monitor process validation, and maintain adherence to current Good Manufacturing Practices (cGMP), GDP, and regulatory norms.
- Quality Assurance: Perform quality checks, maintain product standards, investigate deviations, and manage audits, including those by agencies like US FDA, MHRA, and TGA.
- Resource Coordination: Ensure availability of raw materials, packaging materials, and machine readiness by liaising with procurement and other departments.
- Documentation: Prepare and maintain SOPs, batch records, and other production documentation in line with regulatory and company requirements.
- Team Leadership: Train, supervise, and motivate production staff; enforce company policies, safety procedures, and good manufacturing practices.
- Continuous Improvement: Analyze production data, recommend workflow optimizations, and lead efforts for process and quality improvement.
Educational Qualification
- Minimum requirement: Bachelor’s degree in Pharmaceutical Sciences, Pharmacy, or related disciplines.
- Preferred: Master’s degree and additional certifications in GMP, QA, or production management are advantageous.
- 4–10 years of relevant experience in OSD pharmaceutical manufacturing operations is typically expected.
Key Skills
- Production planning and process validation
- Regulatory compliance and audit handling
- Documentation and reporting
- Leadership, teamwork, and training abilities
- Knowledge of equipment (granulation, compression, coating, etc.) and safety standards
Job Type: Full-time
Pay: ₹25,000.00 - ₹70,000.00 per month
Work Location: In person
