Pharmaceutical production coordinator

Pharmaceutical production coordinator

• Implements Operational manuals, production plans and programs;
• Ensures conformance of manufacturing processes with organizational objectives and policies with the coordination of Production Executive
• Works on the production machines as per SOPs
• Checks the availability of adequate raw and packing materials, utilities, filters and machine size parts;
• Fulfills the monthly and weekly production plans according to the schedule with the coordination of Production Executive
• Monitors drugs manufacturing activities in compliance with the requirements of cGMP;
• Ensures that all standard yield are maintained by production lines;
• Controls production process and production facilities;
• Ensures the general cleanliness and hygienic conditions of the manufacturing areas;
• Ensures that all production equipment is maintained in good working order;
• Assists in pilot scale trials of products under development;
• Ensures that there is discipline and good working culture among the staff;
• Makes sure the on-job training of production personnel;
• Ensures the hygienic condition of production personnel;
• Ensures production people wear mask, gloves and shoes before entering into production;
• Prepares daily reports;
• Performs other duties as assigned by Production Executive
• Responsible for any delay during daily as well as weekly work schedule;
• Decides either to reject or use by sorting non-conforming raw and packing materials discovered during the manufacturing process after discussing with Production Executive
• Takes decision about where engaging man power in absence of work or when making work priorities;
• Responsible for planning of work according to weekly program;
• Mainly supervises duties of subordinates, operators and rest of workers;
• Responsible for materials issued from warehouse for manufacturing;
• Responsible to keep all confidential matters secret and protect the interest of the company.

• Bachelor of Pharmacy;
• Experience with method validation, GMP compliance and experience with creating SOPs is preferred;
• Must have the proven ability to organize and prioritize work for efficient operations;
• Substantial attention to detail is required with any task;
• Proven ability to effectively use Microsoft Office Applications.