Manufacturing Supervisor, Finishing (2nd Shift)
On-siteBloomington, Indiana, United States
Job Summary
Lead the Finishing production area by supervising daily operations, scheduling, staffing, material management, and compliance with cGMP standards. Provide hands-on leadership to direct reports, conducting interviews, mentoring staff, and managing annual performance reviews. Review and approve batch documentation, manage internal audits, and lead technical investigations using Root Cause Analysis tools. Resolve process deviations, support equipment validation, and represent the company during regulatory audits. Maintain high Gemba presence to drive continuous improvement through LEAN principles while ensuring strict adherence to SISPQ standards.
Required Qualifications
- High School diploma or GED
- Minimum 2 years of manufacturing experience
- Minimum 1 year leadership experience
- Required to stand for over 4 hours per day, including constant standing for 2 hours at time
- Duties may require overtime work, including nights and weekends
- Use of hands and fingers to manipulate equipment is required
Desired Qualifications
- In-depth process knowledge of related manufacturing equipment and processes
- Experienced understanding of cGMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry
- Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: Veeva, Trackwise, SCADA (or similar) system, etc.)
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