Manufacturing Supervisor Job at Global Life Science Hub in Chicago

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:

1. 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.
2. Provide coaching, counselling, and development to direct staff, conducting annual performance reviews.
3. Maintain alignment with department goals and objectives.
4. Promote safe work practices and compliance with policies, environmental, health, and safety standards.
5. Train personnel on equipment, processes, and SOPs.
6. Develop and manage packaging schedules within budget.
7. Ensure timely project completion and participate in qualification and validation activities.
8. Investigate and resolve problems, propose process improvements, and foster collaboration.
9. Monitor processes, generate reports, and provide operational direction.
10. Review documentation for compliance standards and establish timelines.
11. Participate in multi-functional project teams and perform additional tasks as required.

Qualifications:

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