This job is closed

We regret to inform you that the job you were interested in has been closed. Although this specific position is no longer available, we encourage you to continue exploring other opportunities on our job board.

Trelleborg - Menomonie, WI

posted about 2 months ago

Full-time - Entry Level
Menomonie, WI
Management of Companies and Enterprises

About the position

The Manufacturing Engineer / Process Engineer at Trelleborg Medical Solutions is responsible for designing and developing efficient engineering solutions for lean manufacturing processes. This role involves validating manufacturing activities in a clean room environment, recommending improvements to production processes, and supporting the launch of new or revised products. The position offers opportunities for growth and advancement within a global company that values internal promotion.

Responsibilities

  • Analyze product specifications and translate these into manufacturing processes to establish production rates and quality levels.
  • Develop manufacturing methods for new and existing products, establish labor standards, and develop product cost information.
  • Perform validation activities in a clean room manufacturing environment.
  • Engage in research and development for equipment, processes, procedures, and systems integration.
  • Document all manufacturing process information and sequences within the site's document control system.
  • Identify opportunities for improvement to existing processes and methods using data or observation, and implement improvements.
  • Make improvements to production rates and reduce scrap by identifying and implementing new equipment or processes.
  • Assist production in troubleshooting production problems and improve situations to assure customer delivery dates and quality.
  • Review production schedules and engineering specifications to resolve production problems.
  • Serve as a member of the CAPA team to implement permanent corrective actions.
  • Participate in determination of product DMR disposition plan and approval.
  • Follow all H&M Quality System protocols including ISO 13485 and 21 CFR part 11 and part 820.
  • Execute DOE's, problem solving, engineering studies, OQ/PQ validations, and continuation engineering for products.
  • Support Production, Engineering, and Quality departments.

Requirements

  • Bachelor's Degree in Industrial, Manufacturing or Mechanical Engineering or related discipline.
  • 2+ years of experience in med device manufacturing (desired).
  • Plastics experience (desired).
  • Training through American Institute of Molding (desired).

Nice-to-haves

  • Proficient in Lean Manufacturing and problem-solving tools such as 5 why, Fishbone, 8D, etc.

Benefits

  • Competitive compensation
  • Generous benefits package including health, dental, vision, STD, LTD, life, 401k, paid time off, tuition reimbursement
  • Paid holidays
  • Growth and advancement opportunities
Job Description Matching

Match and compare your resume to any job description

Start Matching
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service