Production Manager (pharma Industry)
Opal Laboratories (Pvt) Ltd, Pakistan

1 - Qualitative Control:

(a) To ensure compliance to GMP in all areas of production with regards to Man, Machinery, Material, and Area.

(b) To ensure compliance of production operations to written down procedure (SOP) through implementation of sound in-process controls.

(c) To ensure proper documentation of work done and correct filling of BMR, Area Control Records, Equipment and Machine records, Environment and Area Control records and any other document introduced from time to time.

2 - Coordination & Interface

(a) To coordinate with the Product Development Department to have effective interface of Product Development departments man, equipment and machinery needs with production departments own utilization program to achieve its own plan. Also to coordinate with Product Development department to achieve time effective product development and validation of new products commercialization.

(b) To coordinate with the Accounts department to ensure timely audit of completed BMR's and to prepare management reports for deviations.

(c) To interface effectively with ISO, IT and HR departments for continuous development of systems and to ensure effective implementations of modules.

3 - Production & Resource Planning:

(a) To coordinate effectively and timely with Client Services department and Ware House Manager for production plan for the next month and to follow up effectively the resource management (man, material, machine) to achieve the targets .

(b) To improve productivity and yields, reduce losses, down time, and idle time. To improve effective utilization of resources.

(c) To monitor productivity, output, yields, losses, down time, consumption and any other indicators and present a monthly report of performance.

Production Manager (Pharma Industry)