Inspector (Weekend Shift)

Edwards Lifesciences•Salt Lake, UT

About The Position

Performs inspector work to support manufacturing and production activities, following established procedures and guidance. Inspects more complex components and finished medical device products and performs functional testing to confirm conformance with design specifications. The role works with greater independence and a higher level of productivity and may also support inventory control, document verification, and training colleagues from other sites. The position works Friday through Sunday, 5:00 a.m. to 5:30 p.m. Employees are expected to arrive on time, maintain regular attendance without excessive absenteeism, and work an eight-hour or longer work period.

Requirements

  • High school diploma or equivalent.
  • Two years of previous related experience.
  • Previous medical device assembly experience.
  • Ability to read, comprehend, write, and speak English.
  • Basic computer skills, including working knowledge of manufacturing software.
  • Ability to use applicable tools and equipment, with hand-eye coordination and high manual dexterity.
  • Full understanding of applicable inspection procedures.
  • Ability to clearly describe and convey nonconformance issues and enter them into a Quality Management System.
  • Good communication skills and strict attention to detail.
  • Ability to work in a team environment and effectively provide and accept feedback from colleagues.
  • Ability to resolve routine issues with senior staff for supervisory guidance and approval.

Nice To Haves

  • Continuously expands proficiency in inspection techniques.

Responsibilities

  • Perform visual, dimensional, and functional inspections of complex components and/or finished medical device products using tools and equipment such as magnifying lamps, microscopes, and vision inspection systems.
  • Perform functional testing of finished medical device products using automated and manual valve testing equipment.
  • Follow established work instructions and SOPs, record traceable information on device history records, and enter information into JDE when applicable.
  • Verify manufacturing documents against component and device drawings.
  • May control inventory to ensure appropriate storage conditions and movement.
  • May train colleagues from other sites, including inspecting their work output.
  • Provide feedback on product defects and may follow through to establish resolution.
  • Comply with company rules and requirements, including pandemic protocols and Environmental Health & Safety rules, and take adequate control measures to prevent injuries and pollution and protect the environment.
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