Senior Supervisor - Production

Senior Supervisor - Production University of Missouri - 4.1 Columbia, MO Job Details Full-time $80,000 - $100,000 a year 11 days ago Benefits Paid parental leave Caregiver leave Disability insurance Health insurance Dental insurance Paid time off Parental leave Vision insurance Qualifications Performance monitoring Data integrity assurance Employee onboarding Report preparation Manufacturing management Staff supervision Performance improvement leadership Laboratory inventory control Team member evaluation Content creation for technical audiences Quality records maintenance Defect resolution root cause analysis Laboratory document review Procedural guides Coaching Regulatory compliance Technical writing within manufacturing Production deviation management Production risk assessment Production safety compliance Laboratory experience Good documentation practices (GDP) Corrective and preventive actions (CAPA) Team scheduling Performance feedback (performance evaluation method) Change management Team development Hiring Professional development support Bachelor's degree Full Job Description Hiring Department MRR Products & Svcs Mfg Job Description The University of Missouri Research Reactor (MURR) is seeking a Senior Supervisor - Production position that will oversee the Non-Carrier Added Lutecium production team. This position will report to the Manager - Production. The Senior Supervisor - Production will play a critical role in the regular and successful production of Good Manufacturing Practice (GMP) Isotopes This position will be responsible for a team of Technicians that conduct the processes involved with the production and release of these critical isotopes. Key Duties Performed by This Position Will Include Supervise and develop a high-performing production team, including assigning work, setting priorities and expectations, delegating responsibilities, providing routine feedback, completing performance appraisals, coaching and mentoring direct reports, and assisting with hiring and onboarding. Oversee end-to-end cGMP and related production processes, ensuring complex process steps are coordinated effectively and production commitments to customers and patients are met. Promote a safety-conscious, quality-focused, positive, and collaborative work environment through daily leadership, communication, and professional interactions. Support a strong quality culture by reinforcing compliance with procedures, good documentation practices, data integrity expectations, and timely escalation of quality or process concerns. Monitor process performance, including key performance indicators, budget awareness, staffing needs, scheduling, inventory management, and reagent preparation. Coordinate with peers and site leadership to align production activities with departmental, quality, safety, regulatory, and organizational priorities. Drive continuous improvement, change management, process robustness, efficiency gains, and waste reduction while maintaining compliance with quality and regulatory expectations. Identify, assess, escalate, investigate, and support resolution of critical production issues within required timelines using established procedures, root cause analysis, CAPA processes, corrective action implementation, and effectiveness verification. Participate in cross-functional meetings with Production, Quality Assurance, Quality Control, Regulatory Affairs, Development/Translation, Radiation Protection, Shipping, Finance, Reactor Operations, and Safety to provide production updates, share feedback, and support aligned decision-making. Author, review, and revise technical documentation, including SOPs, change controls, deviations, and related production records. Perform other duties as assigned to support production operations, quality objectives, departmental priorities, and site goals.

Shift A/B Shift:

5am-3pm, Monday, Tuesday, Thursday, and Friday (10-hour shifts), with some rotation on the B Shift as needed for processing coverage (8am-6pm). Minimum Qualifications Bachelor's degree or equivalent combination of education and experience and at least 4 years of experience from which comparable knowledge and skills can be acquired is necessary. Preferred Qualifications Preference will be given to those with management experience, cGMP experience, general laboratory experience, and/or regulated manufacturing experience. Experience with technical writing, root cause analysis, effective corrective/preventative action identification, and/or risk assessments.

Anticipated Hiring Range Salary Range:

$80,000.00 - $100,000.00 per year

Grade:

GGS M12

University Title:

MURR Senior Supervisor Internal applicants can determine their University title by accessing the Talent Profile tile in myHR. Benefit Eligibility This position is eligible for University benefits. As part of your total compensation, the University offers a comprehensive benefits package, including medical, dental and vision plans, retirement, paid time off, short- and long-term disability, paid parental leave, paid caregiver leave, and educational fee discounts for all four UM System campuses. For additional information on University benefits, please visit the Faculty & Staff Benefits website at https://www.umsystem.edu/totalrewards/benefits. Equal Employment Opportunity The University of Missouri is an Equal Opportunity Employer. To request ADA accommodations, please call the Director of Accessibility and ADA at 573-884-7278.