About this opportunity
Ametek lists this Production Supervisor opportunity in mansfield, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Production SupervisorLocation: Mansfield, MA, US, 2048 Business Unit: Advanced Medical ComponentsWe are searching for a Production Supervisor to work 1st shift. In this role you will direct and coordinate the work of production employees to meet customer needs and production goals. You'll manage production processes and staff while ensuring that the processes are efficient and safe. You will manage day-to-day production activities, including but not limited, scheduling, organizing work flows, and monitoring and measuring throughput. You will strive to improve safety, quality, delivery, productivity, and cost. This position reports to the Plant Manager and will work in our Mansfield, MA location.ESSENTIAL DUTIES AND KEY RESPONSIBILITIES:Supervises the safe operation of all production processes.Identifies improvements needed and leads project for implementation.Continually monitors area and solicits feedback from employees.Enforce all safety rules and regulations.Is key coordinator/communicator for at least one safety training program for the site.Interviews, selects, orients, trains, conduct performance appraisals, performance development, schedules and approves hours and time off requests.Provides leadership for employee relations through effective communications, coaching, training and development.Executes operational plan to enhance profitability, productivity and efficiency throughout assigned production department(s).Work with others to implement Lean Manufacturing techniques to improve quality, cost, on-time delivery, safety, customer satisfaction, employee satisfaction.Maintains production plan.Ensures compliance with the organization standards for cost control, waste reduction, quality, safety, on-time delivery.Ensures compliance with the organization's policies and applicable laws including OSHA regulations.Provide training and support needed to the team, set goals and objectives.Measure team performance for safety, quality, delivery and cost.Work with team to continually improve these measures.Arrange for equipment, materials and supplies to be available for work assignments.Approve setups and assign operators.Troubleshoot bottleneck operations to determine cause and notify appropriate support for assistance.Check work methods and operations to make recommendations for improving quality and implement systems to report and reduce scrap and cost.Identify opportunities aimed at continuous improvement of the quality of products and processes.Leads project team during identification through implementation and evaluation.Confers with others to coordinate operations and activities across all shifts.Other responsibilities as required including, but not limited to, Manufacturing Associate essential duties and responsibilities.EDUCATION and/or EXPERIENCE:Required: High school diploma or equivalentMinimum of four (4) years of experience in medical device manufacturing environmentKnowledge and experience with GMP, ISO, FDA, and other quality standardsWorking knowledge of Microsoft Office applicationsExperience in a medical device manufacturing environmentDesired: Associate Degree or higherMinimum of 4 years' experience in a leadership roleExperience in the setup and operation of manufacturing processes/equipment.Broad experience with components and assembly.Knowledge of production and processing and other techniques for maximizing the effective manufacture of products.Skills/Competencies:Demonstrated ability to lead people, resolve conflicts and get results through othersExcellent interpersonal and communication skills to work with associates, customers and vendors.Detailed technical knowledge of set-up, assembly and testing procedures, normally attained through years of experience.Ability to understand and interpret basic manufacturing documentation, i.e.: Bills of Materials (BOMs), routers, etc.Ability to implement Kaizen and Lean Manufacturing techniquesHigh attention to detail.Ability to think ahead.Excellent analytical, project and program management skillsAbility to solve practical problems and deal with a variety of changing situationsKnowledge of human resources and safety to include coaching, performance management, OSHA and related safety standards.Ability to think critically and use judgment to identify strengths and weaknesses of solutions to problems presented in production.Ability to multi-task in a fast-paced environment and manage multiple/shifting priorities.Ability to work under minimal direction and self-motivated.Read/write/speak and understand English.Ability to maintain a safe work environment.Paragon Medical, a business of AMETEK, Inc, serves as a strategic partner in medical device manufacturing, offering an end-to-end supply chain solution from initial concept and product development, to verification and validation testing, to final production, assembly, and ongoing strategic demand planning.
Worksite address
mansfield, MA, 02048, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.