Quality Engineering Supervisor

Location

USA - Litchfield

Apply by

2025-02-22

Why Join Us?

As a valued Trelleborg team member, you will enjoy:

  • Greater opportunity for impact
  • Competitive compensation
  • Outstanding benefits package: Health, Dental, Vision, STD, LTD, Life, 401k
  • Generous paid time off
  • Bonus potential

Tasks & Responsibilities:

  • Must be knowledgeable and adhere to TMS Quality Management System and its requirements.
  • Drives and supports QMS initiatives and continuous improvement activities.
  • Ensures direct reports are successfully performing their duties as assigned. Provides coaching on an ongoing basis.
  • Ensure necessary training is defined, assigned, and executed for the direct reports.
  • Assigns projects and responsibilities to the direct reports. Ensures skill sets of staff are in alignment with expected duties.
  • Consults Quality Manager/Director on quality-related topics
  • Establishes and develops site-specific processes as required/requested
  • Reviews and approves processes, Quality Plans, protocols/reports, as necessary.
  • Ensures proper resource allocation to support needs to ensure delivery expectations of customers.
  • Provides recommendations for goals and objectives for the Quality Department
  • Supports and coordinates management of nonconforming issues such as complaints, nonconforming materials and events, audit findings, and CAPAs.
  • Drives best practices through the application of effective quality engineering principals and procedures across functions
  • Ensures proper controls are being systematically applied to products
  • Supports internal and external audits
  • Provides recommendations based on data for improvements that are measurable.
  • Other duties as assigned

Required:

  • 4-year degree in Engineering or Science-related field
  • 4+ years of increasing experience providing technical support and leadership in regulated environment
  • Class I, II, III Medical Device and component manufacturing experience
  • Experience in coaching and utilizing performance management tools and disciplines
  • Extensive experience with statistical analysis, Minitab software (or equivalent), GD&T and CAPA investigation and resolution

Desired:

  • Knowledge and experience with one or more: ISO/FDA: ISO 9000/9001; ISO 13485, and 21CFR Part 11/820 (and 4/210/211 as applicable)
  • Quality certifications (ASQ CQE, CQA, CQM, etc.)
  • Experience auditing (internal and external) for all elements of ISO 9001 and/or ISO 13485
  • Experience with the successful completion of multiple projects for new product development or improvement initiatives
  •  

Apply

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