Responsible for the supervision of the manufacturing personnel and maintains manufacturing schedules according to requirements on a daily or weekly basis. Checks all manufacturing batch records for completeness, corrections and approval. Coordinates and gives periodic trainings and meetings for all manufacturing personnel regarding safety, production needs, cGMP's, company policies, etc. Maintains communication with the Department Manager in regard to the welfare and performance of the manufacturing personnel. Prepares periodic merit evaluations of his subordinates, ensure all payroll adjustments are made and verify job schedules for his subordinates are completed accordingly. Stresses the adherence to written procedures and all safety, health, security and personnel regulations. Responsible for the correction of any deviation of the Current Good Manufacturing Practices within the manufacturing areas and responsible for cGMP audits and reports with their proper follow-ups (within the department). Controls Inventory weigh-out deduction cards for the weighing area and verifies proper control of expiration dates of any material. Reconciles the batch of tablets/capsules processed and explains any abnormal yield of tablets/capsules.

Minimum of a Bachelor's degree of Science or related area is required and 2-4 years of experience in the Pharmaceutical Industry or specialized area is required. Must possess written and verbal communications skills in both, English and Spanish. Must be proficient on the computer and have a working knowledge of Microsoft Office (Word, Excel, Power Point). Must be able to judge when a given situation should be brought to the attention of the Manager of Production. Good judgment is necessary in order to insure the quality of the product and the maximum of productivity. Must possess strong analytical, interpersonal, supervisory, and problem solving skills. (Caguas Area)



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