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Job #02863

About our client Our client is a leading manufacturer of injectable products in the pharmaceutical industry. The maker of multi-source and branded products has been in operation since 1996. The company is an expert in acute medical care and caters to both patient and ambulatory settings. It helps millions of people across North America fight critical illnesses by providing ongoing affordable healthcare. The company is in a continuous expansion mode and has a portfolio of products covering a wide range of therapeutic segments. Position Location Production Supervisor – 3rd Shift Chicago, Illinois Salary Highly competitive package, commensurate with experience Responsibilities 1) Supervise and coordinate the activities of employees engaging in component preparation, filling, capping, autoclaving, terminal sterilization, compounding and lyophilization production 2) Ensure that proper systems and resources are in place to meet production schedules on time 3) Supervise manufacturing group leaders and hourly staff in proper operating techniques and procedures 4) Ensure that the product is manufactured to specification and as per SOPs, cGMPs and safety procedures 5) Develop information and compile reports concerning scheduling, production goals, equipment and maintenance problems as well as other studies (as requested) 6) Assist in establishing production schedules 7) Confer with other departmental managers to coordinate the scheduling of operations to achieve required deadlines 8) Develop departmental employees through orientation, training, establishing objectives, communicating rules and policies while building employee morale and motivation 9) Maintain compliance with company policies, cGMPs, safety standards and good housekeeping practices 10) Monitor and control production schedules and activities to ensure meeting of departmental performance objectives and budgets 11) Supervise, coordinate and control production and operating activities to ensure optimum utilization of personnel, materials and equipment 12) Conduct continuous reviewing and follow-up on projects to ensure completion of assigned work 13) Evaluate the performance and production of staff 14) Maintain records on performance 15) Advise departmental managers on matters related to daily operations and make recommendations for improvements (when feasible) 16) Recommend and implement value- and process-improvement programs 17) Ensure that adequate resources are available to manufacture product (equipment, supplies and labor) 18) Perform/ensure investigations and document corrections/modifications are done effectively and in a timely manner Requirements 1) Associate degree or technical certification 2) 5 years of pharmaceutical manufacturing experience 3) 2 years of experience as a Supervisor (supervising manufacturing group leaders) 4) Experience in and knowledge of cGMP