2nd Shift Medical Device Inspector – Quality Impact

Edwards Lifesciences

Salt Lake City (UT)

On-site

USD 30,000 - 33,000

Full time

14 days+

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Job summary

Edwards Lifesciences in Salt Lake City is seeking a Quality Inspector to support our medical device manufacturing. You will perform visual, dimensional, and functional inspections on components and finished products, ensuring conformance to design specifications.

The role includes testing with automated and manual equipment, following SOPs, recording traceable data to device history records, and collaborating with cross-functional teams to maintain the highest standards of quality and patient

Qualifications

  • HS diploma or equivalent is required.
  • Must be able to read, write, and speak English.
  • Strong attention to detail and steady hands.
  • Basic understanding of inspection procedures.

Responsibilities

  • Perform visual, dimensional, and functional inspection of components and finished medical device products using tools and equipment to ensure conformance with design specs.
  • Perform functional testing of finished products using automated and manual testing equipment to ensure conformance with design specs.
  • Follow and document work instructions and SOPs, recording traceable information on device history records and entering data into JDE as needed.
  • Verify manufacturing documents against component and device drawings.
  • May control inventory to ensure proper storage and movement of materials.
  • May train colleagues from other sites on inspection output.
  • General housekeeping and safe work practices in the work area.

Skills

Manual dexterity
Attention to detail
Good communication skills
Teamwork

Education

High School Diploma or equivalent

Tools

Vision inspection system
Measurement tools
JDE

Job description

Edwards Lifesciences in Salt Lake City is seeking a Quality Inspector to support our medical device manufacturing. You will perform visual, dimensional, and functional inspections on components and finished products, ensuring conformance to design specifications.

The role includes testing with automated and manual equipment, following SOPs, recording traceable data to device history records, and collaborating with cross-functional teams to maintain the highest standards of quality and patient

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