What are the responsibilities and job description for the Manufacturing Supervisor position at Global Life Science Hub?
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:
If you're interested, please apply below. If this position doesn't interest you, please visit our website for a list of more vacancies - www.glshub.com
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
- 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
If you're interested, please apply below. If this position doesn't interest you, please visit our website for a list of more vacancies - www.glshub.com
