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Edwards Lifesciences

Inspector - Receiving Inspection - Evening Shift

Edwards Lifesciences

Limerick, County Limerick, Ireland · Tempo total

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Experiência
2+ yrs
Salário
Vagas
1
Publicado
há 3 horas
Work mode
No escritório
Educação
H.S. Diploma or equivalent preferred
Eligibility
Candidates with experience in quality inspection or warehousing who can work the specified evening schedule in Limerick and meet the outlined quality, safety, and communication expectations are suitable.
Resume
Required to apply

Where you'll work

Descrição da vaga

Role summary

The Receiving Inspector is responsible for checking incoming components and devices to confirm they satisfy regulatory expectations, internal company standards, and the functional requirements built into the design.

Working hours

This role follows an evening schedule from Monday to Thursday, 4:30 PM to 3:00 AM, with Thursday ending at 2:00 AM.

Key responsibilities

  • Carry out visual, dimensional, and functional checks on parts and devices using tools and equipment such as a magnifying lamp, microscope, vision inspection system, and calipers, while working with a high degree of independence and productivity.
  • Compare receiving paperwork against component and device drawings to verify that all requirements have been satisfied.
  • Complete work according to approved instructions and SOPs, including recording traceability details in device history records and entering data into JDE.
  • Maintain inventory controls by ensuring proper storage conditions, correct movement of materials, and accurate product-status labeling.
  • Support cross-site training by instructing colleagues from other locations and reviewing the quality of their work.
  • Handle additional tasks such as keeping the work area tidy and attending training for new procedures and processes.

Required qualifications

  • A high school diploma or equivalent is preferred.
  • At least 2 years of relevant experience in quality inspection or warehousing is required.

Preferred profile

  • Strong understanding of inspection methods and procedures.
  • Ability to keep building expertise in inspection techniques.
  • Comfortable using inspection tools and equipment, with good hand-eye coordination and fine motor control.
  • Capability to explain nonconformance issues clearly and document them in a Quality Management System.
  • Able to give and receive feedback effectively during independent verification work.
  • Can raise product defect concerns and follow them through to resolution.
  • Good communication ability, including strong English reading, comprehension, speaking, and writing skills.
  • Solid computer skills, including working knowledge of manufacturing software.
  • Very strong attention to detail.
  • Willingness to follow environmental, health, safety, and quality standards for clean-room medical device manufacturing.
  • Able to work with limited supervision and contribute positively in a team setting.
  • Committed to company rules and operational requirements, including safety, illness-prevention, pollution-prevention, and any applicable health and safety protocols.

Additional information

Applicants should be prepared to work in a medical device manufacturing environment and follow all relevant clean-room, quality, and safety expectations.

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