Edwards Lifesciences

Senior Inspector

Edwards Lifesciences

Singapore · Full Time

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Experience
4+ yrs
Salary
Openings
1
Posted
1 week ago
Work mode
In office
Education
Secondary education
Resume
Required to apply

Where you'll work

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Job description

About the Role

Join Edwards Lifesciences' Manufacturing team in Singapore and contribute to innovative medical devices that positively impact patient lives worldwide. The Senior Inspector is vital in ensuring that our products meet the highest quality and regulatory standards through detailed inspection and testing.

Key Responsibilities

  • Conduct thorough visual, dimensional, and functional inspections on components and finished medical devices using diverse tools and equipment to confirm compliance with design criteria.
  • Perform functional tests on completed medical devices utilizing both automated and manual valve testing systems.
  • Verify quality documentation including Device History Records and oversee product releases for intra-plant shipments or distribution, potentially applying Geometric Dimensioning and Tolerancing methods.
  • Manage inventory control to maintain suitable storage conditions and ensure proper movement of materials.
  • Maintain general housekeeping within the work area to support a clean and safe environment.

Required Qualifications

  • Secondary education completed; additional technical training is desirable.
  • Minimum of 4 years experience in manufacturing and quality control roles.

Preferred Skills and Attributes

  • Strong interpersonal and communication skills with an aptitude for training others in processes and methodologies.
  • Proficient in English reading, writing, speaking, and comprehension.
  • Solid computer literacy including familiarity with manufacturing software tools.
  • Exceptional hand-eye coordination and manual dexterity for equipment operation.
  • Deep understanding of inspection procedures, with experience contributing to procedural development.
  • Expertise in diverse production inspection techniques.
  • Capable of documenting and reporting nonconformities accurately within a quality management system (QMS).
  • Experience with programming and validating automated test equipment.
  • Meticulous attention to detail and ability to work collaboratively within teams and cross-departmentally.
  • Ability to provide and receive constructive feedback effectively.
  • Strict compliance with corporate rules such as safety protocols, environmental health regulations, and pollution prevention measures.

Minimum education

Secondary (Class 10)

Industry

Medical Devices

How they work

Communication Teamwork & Collaboration Attention to Detail Initiative Accountability

Languages

English
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