Aseptic Manufacturing Supervisor

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.