Aseptic Manufacturing Supervisor

4 weeks ago

Chicago, United States Global Life Science Hub Full time
Job DescriptionJob Description

Our client, a leading pharmaceutical company, is experiencing rapid growth and seeking a talented Manufacturing Supervisor (DP) to join their dynamic team in Chicago, IL. As a Manufacturing Supervisor (DP), you will play a crucial role as a shift leader in their manufacturing operation. Your responsibilities will include ensuring the production of high-quality products in compliance with regulatory requirements, operational plans, and company policies. Join our client's team and make a significant impact on their success

Responsibilities:

  • Supervise and guide production floor personnel to ensure efficient use of equipment and materials for high-quality product outcomes in accordance with cGMP and production plan.
  • Provide coaching, counselling, and development to direct staff, conducting annual performance reviews.
  • Maintain alignment with department goals and objectives.
  • Promote safe work practices and compliance with policies, environmental, health, and safety standards.
  • Train personnel on equipment, processes, and SOPs.
  • Develop and manage packaging schedules within budget.
  • Ensure timely project completion and participate in qualification and validation activities.
  • Investigate and resolve problems, propose process improvements, and foster collaboration.
  • Monitor processes, generate reports, and provide operational direction.
  • Review documentation for compliance standards and establish timelines.
  • Participate in multi-functional project teams and perform additional tasks as required.

Requirements:

  • Bachelor's degree in engineering, pharmaceuticals, related life sciences, or equivalent with 4+ years of experience.
  • Master's degree in engineering, pharmaceuticals, related life sciences, or equivalent with 2+ years of experience.
  • Preferred experience in aseptic processing, manual visual inspection, and finished product packaging with serialization.
  • Strong communication, leadership, and problem-solving skills.
  • Proficient in technical writing, MS Office applications, and leading operational teams.
  • Familiarity with FDA cGMPs and regulations.
  • Ability to work in office and biotechnology manufacturing environments.
  • Flexibility for different shifts, overtime, and travel.

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