Job Description
- Batch Production: Overseeing the production of chemical compounds or pharmaceutical products in accordance with predefined recipes and production procedures
- Quality Control: Monitoring and ensuring the quality of products by conducting quality control tests and inspections at various stages of production
- Process Optimization: Identifying opportunities for process improvements to increase production efficiency, reduce waste, and enhance product quality
- Equipment Operation: Operating and maintaining production equipment, including reactors, distillation units, and filtration systems
- Safety: Adhering to safety protocols and procedures to prevent accidents and exposure to hazardous chemicals
- GMP Compliance: Ensuring that production processes adhere to Good Manufacturing Practices (GMP) and regulatory standards
- Raw Material Handling: Managing the procurement and handling of raw materials, ensuring their availability for production
- Record Keeping: Maintaining accurate records and documentation related to production activities, including batch records, testing results, and equipment maintenance logs
- Troubleshooting: Identifying and resolving production issues, such as deviations, out-of-spec results, or equipment malfunctions
- Environmental Compliance: Ensuring that production processes are in compliance with environmental regulations and safety standards
- Waste Management: Properly managing and disposing of hazardous waste generated during the production process
- Cleaning and Maintenance: Overseeing the cleaning and maintenance of production equipment and facilities to ensure proper functionality
- Scale-Up: Participating in scale-up processes, which involve transitioning laboratory-scale processes to full-scale production
KEY SKILLS: Pharma, GMP, Management
EXPERIENCE: 3 – 4 years
QUALIFICATION:
B.Sc in Chemistry
MS/M.Sc(Science) in Chemistry