Pharmaceutical Granulation Supervisor
Caraco Pharmaceutical Laboratories - Detroit, MI

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Purpose:

Responsible for the direction and coordination of single shift team; focus results in a timely and effective manner. Ensure the manufacturing of products are in accordance with production budgets, quality, safety standards and all regulatory requirements.

Essential Duties:
  • Ensure that all products are manufactured according to Quality standards and product specifications through daily execution of batch master records
  • Perform the documentaion and reconciliation of batch master records
  • Directs and coordinates the activities of department operators through development of shift plans and supervision
  • Oversee ERP database
  • Participates with materials management. QA and Tech services in the execution of production plans and projects to meet forecast needs
  • Establish, maintain, and continually analyze production control and documentaion procedures to assure departmental compliance with cGMP, improve yields and reduce cost
  • Develop, train and motivate hourly personnell
  • Review the production planning and prepare the daily planning to achieve the production targets
  • Prepare and revise SOP's and Work Instructions
  • Track Preventaive maintenance plans of all machine and tracking of the calibration requirment of all instruments
Job Qualifications:
  • Solid and working knowledge of cGMP regulations and safety procedures
  • Mimimum 2yrs supervisory experience in pharmaceutical manufacturing industry

Education:

Associates or Bachelors degree in Science

Caraco Pharmaceutical Laboratories - 19 months ago - save job - block
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