Trelleborg AB

Metrology Engineer

Trelleborg AB$75K — $90K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 4-year degree in quality, manufacturing, engineering, or related field or equivalent experience
  • Experience in regulated manufacturing industry
  • 2+ years in a regulated manufacturing environment preferred
  • Quality certifications (e.g. ASQ CQE, CQT, CQA) desirable
  • Familiarity with GMP/ISO standards and medical device regulations

Responsibilities

  • Develop measurement methods for compliance with medical device quality regulations
  • Conduct test method validation, including sample creation and documentation
  • Calibrate measurement instruments and perform maintenance as needed
  • Create robust measurement systems and program automated test equipment
  • Analyze Geometric Dimensioning and Tolerancing (GD&T) specifications for testing
  • Support metrology projects by interpreting technical documents and specifications
  • Plan and coordinate Test Method Development and validation activities

Benefits

  • Comprehensive health, dental, and vision insurance
  • Short-term and long-term disability coverage
  • Life insurance
  • 401(k) with employer match
  • Paid time off and tuition reimbursement
  • Clean, climate-controlled work environment
  • Opportunities for internal promotions and career advancement
Full Job Description
Trelleborg Medical Solutions is seeking a Metrology Engineer to join the team in the Delano, MN area.

If you have proven Quality and Metrology experience in a manufacturing environment, this is an opportunity you need to explore!

As a valued team member with Trelleborg, you will enjoy:

  • Competitive compensation: $75-90k DOE + bonus opportunities!
  • Generous benefits package: Includes health, dental, vision, STD, LTD, life, 401k, paid time off, tuition reimbursement, and more!
  • Clean work environment: Enjoy working in a very clean and climate-controlled environment every day!
  • Greater opportunity for impact: You will have the autonomy and support to lead the production team and impact the production of life-saving devices.
  • Growth and advancement: Join a global company that loves to promote from within and allows for advancement into one of their many other U.S. locations!


The final compensation offered to the candidate may be based on geographical location, work experience and/or skill level. Additions to the compensation packing, including but not limited to paid time off, insurance benefits and 401(k) eligibility, will be outlined at the time of the job offer.

Job Responsibilities:

  • Complete tasks related to measurement method development and support in compliance with quality regulations for medical device manufacturing
  • Setup and conduct test method validation for variable and attribute test method validation activities, including sample creation, developing test method work instructions
  • In coordination with site the quality team, calibrate measurement instruments and equipment at regular intervals, and perform preventative maintenance when applicable
  • Develop robust measurement systems per medical device requirements, program CMM and automated vision systems, develop test methods for hand tools and gages
  • Review, interpret, and analyze Geometric Dimensional and Tolerance (GD&T) requirements per specifications to perform test method development and validation
  • Interpret specifications, drawings, customer documentation and other documents as necessary to support metrology projects
  • Plan, coordinate, conduct Test Method Development and Validation activities, Initiate inspection plans for new/revised product


Education and Experience:

  • Required:
    • 4 year degree in quality, manufacturing, engineering, or related equivalent experience
    • Regulated manufacturing industry experience

    Desired:
    • 2+ years of regulated manufacturing
    • Quality certification(s) (e.g. ASQ CQE, CQT, CQA, ).
    • Class I, II and/or III Medical Device manufacturing
    • Knowledge and experience with GMP/ISO


Competencies:

  • Ability to read, write, speak and understand the English language (with a help of a translator, if needed)
  • Ability to communicate clearly by conveying and receiving ideas, information and direction effectively
  • Ability to demonstrate adequate job knowledge to deliver a world class performance
  • Ability to challenge oneself to consistently meet all goals and deadlines
  • Willingness to strive for excellence by producing work that is free of errors and mistakes
  • Desire to delight both customers and coworkers by offering encouragement, fostering teamwork and addressing conflict appropriately
  • Commitment to making improvements company wide
  • Demonstrated competence using Microsoft Office, Project, Access and JMP
  • Comprehensive understanding of applicable Work Instructions, SOP'S, and ISO standards
  • Working knowledge of statistical methods associated with six sigma and quality
  • Able to perform math functions
  • Effective project leader
  • Experience with lean manufacturing principles and their implementation
  • Good hand/eye coordination and depth perception
  • Good manual dexterity
  • Correctable normal reading distance vision


Travel requirements:

Travel as required between Delano, MN and Litchfield, MN along with global site support. Some international travel is required.

About Trelleborg AB

Trelleborg AB is a global engineering group focused on polymer technology, with headquarters in Trelleborg, Sweden. The company operates in three main business areas: Trelleborg Industrial Solutions, Trelleborg Sealing Solutions, and Trelleborg Wheel Systems. Trelleborg's products are used in a wide range of industries, including aerospace, automotive, construction, healthcare, and oil and gas. The company has operations in over 50 countries and employs approximately 24,000 people. Trelleborg is listed on the Stockholm Stock Exchange and has a market capitalization of approximately SEK 50 billion.
Learn more about Trelleborg AB
Size
24,000 employees
Industry

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