Supervisor Production
Company: Curium
Location: Noblesville
Posted on: March 3, 2026
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Job Description:
Summary of Position The Production Supervisor is responsible for
the oversight of manufacturing operations associated with the
manufacturing of radiopharmaceuticals which meet approved
specifications by supervising from the floor, coaching and
developing their team, and ensuring that their area of operations
maintains compliance with Corporate policies, and local and federal
regulations. The Supervisor is responsible for fostering a culture
of team ownership, transparency, team success. Work Schedule:
Friday through Tuesday 4pm - 12:30pm, schedule is subject to
change. Essential Functions Ensure proper coverage of all
production while also managing team PTO, trainings, absences, and
other events impactful to staffing. Ensure accountability,
transparency, and effective communication cross-functionally and
within the team while guaranteeing information is timely, clear,
and accurate. Review and approve weekly departmental schedules and
maintenance activities; work with multiple departments to ensure
efficient scheduling and planning in order to meet the production
plans. Ensure appropriate communication on production and project
related matters with area management in a timely manner. Coach and
develop the team to high performance while fostering a culture of
team ownership. Verify, review and make appropriate changes if
needed, to any controlled document pertinent to your area of
responsibility. Ensure all employees are in compliance with all
policies, procedures, and site/company regulations. Set clear
vision by ensuring goals and objectives are aligned with site
strategies through performance management for each team member.
Exhibit accountability and responsibility for an area or process in
order to affect change and lead efforts and ideas to completion.
Provide input on equipment installation, start-up, operation, and
troubleshooting. Provide leadership for employee relations through
effective communications, coaching, training and development;
eliminate roadblocks in order for the team to move forward. Supply
the highest level of internal and external customer service while
having the ability to diplomatically challenge established
procedures and systems. Lead and/or support all investigations,
manufacturing exceptions, product failures, Root Cause Analyses,
and customer complaints at the appropriate level with complete and
comprehensive detail. Author, approve, and/or review all area
quality and safety exceptions and investigation reports. Ensure on
time completion of all corrective action items assigned to area.
Manage the department’s overtime and ensure that all payroll
exception reports are completed and submitted on time. Lead team in
continuous improvement activities and take control when faced with
adversity while incorporating team input. Measure and communicate
team’s progress against individual, team, site goals, and KPIs.
Communicates issues appropriately utilizing the area’s escalation
plan. Spend 70% of your time on the production floor directly with
employees and processes. Must maintain operational compliance with
US and international regulatory agencies and guidelines (i.e. FDA,
DEA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.). Ensure all
direct reports are properly trained in areas directly related to
their job responsibilities as well as company policies, quality
policies, and safety/environmental policies. Conduct Production
Team meetings as well as 1-on-1 coaching sessions with employees in
the department. Requirements Bachelor of Science degree in
Manufacturing, Engineering, or related field required. Work
experience considered in lieu of degree. Ten or more years of
relevant work experience required, including experience in a cGMP
environment required, preferably in manufacturing. Two or more
years of supervisory experience is required. Lean/Kaizen/Six Sigma
experience preferred. Experience working with High Performance
Teams. Coaching & Implementing Autonomous Maintenance activities
preferred. Experience with developing/documenting procedures
required. Aseptic and/or terminal sterilization processing
experience preferred. Prior experience leading projects and/or
being a core team member preferred. Working Conditions: Willingness
to work in plant producing radioactive materials and requiring all
employees to participate in safety programs designed to minimize
potential and/or actual exposure levels. Responsibilities include
the ability to lift up to 70 pounds, kneeling, crouching, twisting
the upper body, walking, bending, stooping, pushing, pulling,
reaching, must be able to physically negotiate stairs and
evacuation ladders with or without accommodation, wear and operate
safety equipment, enter vessels, and inspect equipment. Material
handling devices (e.g., hand truck, fork truck, and conveyors) are
used when possible, however, use of proper lifting and movement
techniques is necessary to prevent injury. Must be willing to wear
a variety of Personal Protective Equipment (PPE) and hearing
protection as needed. May be required to sit or stand for long
periods of 8 hours a day while performing duties. Must possess good
hand-eye coordination; close attention to detail is required. Must
be able to work indoors and outdoors with exposure to
mechanical/moving parts, hazards including corrosive, flammable and
toxic material, dust, dirt, odors, and irritants. Willingness to
complete safety training within allotted timeframes, and work in a
team-based environment. Must be able to work outside of regular
work hours, including off shift, weekend, and holiday work as
business needs require.
Keywords: Curium, Dayton , Supervisor Production, Manufacturing , Noblesville, Ohio
