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Sr. Supervisor, Manufacturing/122750/Cleveland
Sr. Supervisor, Manufacturing/122750/Cleveland-March 2024
Cleveland
Mar 30, 2026
About Sr. Supervisor, Manufacturing/122750/Cleveland

  This Position is for a Sr. Supervisor, Manufacturing - 2nd Shift with a company located in Cleveland.

  Job Summary: You will supervise daily activities in the production area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (cGMPs), SOPs, environmental health and safety (EHS) guidelines and any other regulations that may apply. Monitor and insure efficiency and effectiveness in various areas. Ensure operational efficiency, troubleshoot and investigate as vital. Perform all duties with a focus on optimizing safety, quality, service and cost. May supervise more than one department. Your role as a Supervisor positions you to be directly involved in the physical production that enables Baxter to fulfill our mission to save and sustain lives. You will manage the line between meeting production timelines and making quality products. As a manager, you are the trusted critical connection between the business and the workers on the floor.

  Duties And Responsibilities: Total compliance with all applicable specifications, SOPs, FDA regulations (GMPs) and new drug applications. Technical expertise and direction are provided to all quality and manufacturing operations in order to facilitate successful completion of routine tasks, as well as, product/process improvements and problem solving. Must interface with various support departments such as QM, Engineering, Maintenance, Scheduling, Accounting, and Human Resources. Responsible for adequacy of Specifications and SOPs to assure all products meet the requirements for quality, safety, and integrity. Improve quality and reduce customer complaints through a proactive program that includes interaction with internal and external suppliers to improve quality of incoming materials and utilize collective data from customers to enhance quality of the product, as perceived by the customer. Plan, develop and manage shift teams that monitor, predict or regulate all steps of manufacturing.

    These activities are accomplished through statistical sampling, product auditing and process control. Assist in the validation of new equipment, process, systems, and changes that impact product quality. Represent the company during FDA inspections.

    Provide information as necessary to FDA that established creditability and demonstrated compliance with GMPs. Review, approve, and manage documentation for batch and system records.

    Assist in the release for distribution.

    Assist in meeting product release time goals. Create an environment that stresses and encourages teamwork. Support and encourage all plant activities, i.e., VIPs, QLP, CIs, TPM, Business Process teams Supervise Injection/Husky/LSR operations and staff. Payroll, Production input and reviews. Conversion loss reduction. Responsible for Quality, Production and overall operating performance of the assigned shifts. Will have knowledge of both plant and department environmental health and safety regulations and comply with said regulations accordingly. Will manage multiple shifts and/or multiple departments Will perform all other duties and responsibilities as determined by supervision/management.

  Education and Qualifications:

    Bachelor's degree preferred; minimum Associates degree required, with technical discipline preferred. 3 years or more manufacturing and Plastic injection molding experience highly desirable and 2 years or more of supervisory experience Substantial interpersonal skills both verbal and written for interaction with plant management and subordinates. Computer skills to include Word, Excel, PP and JDE. Lean six sigma training/green belt desirable. Audiometric testing required and hearing protection required. Ability to stand for long periods of time. Ability to work occasional off shifts to monitor work performance and meetings.

  Benefits: We understand compensation is an important factor as you consider the next step in your c reer. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $72,000.00 - $99,000.00 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

  AAP/EEO Statement: Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. EEO is the Law EEO is the law - Poster Supplement. Pay Transparency Policy. Reasonable Accommodations: Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

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