Edwards Lifesciences

Senior Technician, Maintenance/Manufacturing Support Engineer

Edwards Lifesciences · Singapore, Singapore, Singapore

Medical Equipment Manufacturing · 10,001+ employees

15 h ago
Mid (2-5 yrs) Full-time Singapore
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About the role

Perform preventive maintenance and corrective actions on manufacturing equipment to ensure operational efficiency. Conduct experiments and validation tests while documenting findings to support engineering improvements and process optimization.

What they look for

Preventive maintenance Equipment troubleshooting Manufacturing support Root cause analysis Validation Qualification Good documentation practices Technical reporting Process improvement Medical device manufacturing Electrical systems Mechanical systems Pneumatics Controls JDE QMS

Requirements

Requires a diploma with 4 years of experience or an associate's degree with 2 years of experience in a manufacturing or medical device environment. Candidates must possess strong troubleshooting skills and knowledge of electrical, mechanical, and pneumatic systems.

Full description

Make a meaningful difference to patients around the world. At Edwards Lifesciences facilities around the world, our Manufacturing teams create the tools, technologies, and devices that transform patients’ lives. As part of our sewing, assembly, delivery, and distribution teams, your attention to detail and commitment to continuous improvement will help us turn innovative ideas into reality. Your purpose-driven work will help leave lasting and positive impacts on patient lives.

Provide technical manufacturing support to Operations and Engineering.

How you’ll make an impact:

  • Perform weekly preventive maintenance routines for equipment to avoid program down time
  • Check for failures in equipment and perform corrective actions to affected areas that have down time, including conducting and writing impact assessment reports of incidents
  • Execute experiments and tests (following protocols) to develop findings for the validation and improvement of equipment and manufacturing processes/methods based on engineering principles; analyze results, make recommendations, and develop reports for Engineering review
  • Review documentation and take appropriate actions to ensure that information is appropriately catalogued and follow through to validation and qualification of equipment, including transferring information to appropriate locations, e.g., ECRs, SOPs, drawings, and tooling, for Engineering approval
  • Identify potential improvement opportunities and propose solutions to optimize equipment, e.g., re-design/design of basic equipment, tools, fixtures, for Engineering review
  • Troubleshoot basic manufacturing equipment
  • May lead small projects related to new equipment validation, equipment investigations, testing, objective evidence of product dispositions and rework
  • Utilize manufacturing software (e.g., JDE, QMS,PLM) to update documentation in systems
  • Provide coaching and guidance to technicians
  • Other incidental duties

What you'll need (Required):

  • Diploma or equivalent with 4 years of related experience required or
  • Associate's Degree or equivalent with 2 years of related experience required
  • Previous experience in manufacturing and/or medical device experience preferred

What else we look for (Preferred):

  • Good written and verbal communication, interpersonal, and relationship building skills
  • Problem solving methodology, root cause analysis, and GDP (Good Documentation Practices)
  • Good computer skills, including usage of MS Office Suite
  • Moderate knowledge of validation and improvement of automated equipment
  • Ability to troubleshoot manufacturing equipment
  • Basic knowledge of material compatibility in the proposed use environment
  • Moderate knowledge of routine preventive maintenance of production equipment
  • Moderate knowledge electrical, mechanical, electronic, pneumatic, and controls
  • Knowledge of and adherence to Edwards Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
  • Knowledge of Good Manufacturing and Good Documentation Practices supporting a medical device environment
  • Strict attention to detail
  • Must be able to work under limited supervision
  • 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