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Senior Inspector, Pilot

Edwards Lifesciences

Irvine, CAOnsitePosted 10 days ago$51,000 - $70,000/year
Full TimeMid LevelQuality (QA / QC)Medical Device
Original posting ↗

Summary

The Senior Inspector supports manufacturing/production activities, following established procedures and guidance.

Job description

How you'll make an impact

  • Performing visual, dimensional, and functional inspection across all components and/or finished medical device products using a wide variety of all applicable tools and equipment such as magnifying lamp, microscope, vision inspection system, etc. to ensure conformance with design specifications - working independently at the highest levels of productivity.
  • Performing functional testing of finished medical device products using both automated and manual valve testing equipment to ensure conformance with design specifications.
  • Reviewing, following and performing job functions in compliance with established work instructions and adherence with SOPs, including recording traceable information on device history records and may enter information into JDE.
  • Performing verification of manufacturing documents with component and device drawings, which may include Geometric Dimensioning and Tolerancing methodologies.
  • Other incidental duties assigned by leadership: Train colleagues from other sites, including inspection of their work. Provide coaching and training to lower-level employees, evaluate and demonstrate correct approach on work of other employees, able to fill-in for Lead as needed. On time arrival to work, regular attendance without excessive absenteeism, and working a full 8 hour or longer work period.

What you'll need (Required)

  • 4 years of related experience in electronics or medical device industry
  • Due to the specific duties of this job, you must be able to read, comprehend, write, and speak English.
  • Good computer skills, including working knowledge of manufacturing software.
  • Candidate will be required to pass basic English skills assessment.

What else we look for (Preferred)

  • Ability to use applicable tools and equipment, hand eye coordination, and high manual dexterity.
  • Strong communication skills and interpersonal relationship skills, including ability to convey training in methodology and procedures.
  • Full understanding of applicable inspection procedures, including the ability to contribute to the development of procedures.
  • Proficient in all inspection techniques for production inspection.
  • Ability to clearly describe and convey nonconformance issues, and enter them into QMS.
  • Ability to program and contribute to the validation of automated test equipment.
  • Must be able to work in a team environment and with minimum supervision by following detailed work instructions and filling in for Lead as needed.
  • Propose modifications to work assignments and/or station set-ups to maintain smooth workflow.
  • Ability to effectively provide and accept feedback from colleagues as well as provide feedback on product defects and follow through to establish resolution.
  • Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control.

Requirements

  • 4 years of related experience in electronics or medical device industry
  • Must be able to read, comprehend, write, and speak English
  • Good computer skills, including working knowledge of manufacturing software
  • Candidate will be required to pass basic English skills assessment
  • Ability to use applicable tools and equipment, hand eye coordination, and high manual dexterity
  • Strong communication skills and interpersonal relationship skills
  • Full understanding of applicable inspection procedures
  • Proficient in all inspection techniques for production inspection
  • Ability to clearly describe and convey nonconformance issues, and enter them into QMS
  • Ability to program and contribute to the validation of automated test equipment
  • Must be able to work in a team environment and with minimum supervision
  • Propose modifications to work assignments and/or station set-ups to maintain smooth workflow
  • Ability to effectively provide and accept feedback from colleagues
  • Adhere to all company rules and requirements

Benefits

  • Competitive salaries
  • Performance-based incentives
  • Diverse benefits programs

Company overview

Edwards Lifesciences (NYSE: EW) is the leading global structural heart innovation company, driven by a passion to improve patient lives. Founded in 1958 and headquartered in Irvine, California, the company specializes in developing breakthrough technologies for cardiovascular diseases. As a pioneer in the medical device industry, Edwards focuses on transcatheter heart valves, surgical heart valves, hemodynamic monitoring systems, and vascular solutions. The company's patient-focused culture inspires its 16,000+ employees worldwide to deliver life-changing innovations that address complex heart health challenges. Edwards serves patients in over 100 countries through its comprehensive portfolio of products including the SAPIEN transcatheter heart valve system, INSPIRIS surgical valves, and advanced monitoring technologies. With a commitment to research and development, the company invests 17-18% of its revenue back into R&D efforts, maintaining its position at the forefront of structural heart innovation. Edwards Lifesciences has impacted over one million patients globally through its transformative medical technologies.

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