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Edwards Lifesciences

Develops transcatheter heart valves and devices

Lead Manufacturing Technician

Equipment MaintenanceConfirmed live in the last 24 hours
Full-timeLimerick, IrelandNo salary listed

About the Job

Requirements

  • A recognized trade qualification or relevant third-level qualification, plus relevant manufacturing, engineering, or medical device industry experience.
  • A minimum of 6 years of related experience.
  • Strong written and verbal communication, interpersonal, and relationship-building skills.
  • Knowledge of problem-solving methodology, root cause analysis, and Good Documentation Practices.
  • Strong computer skills, including use of the Microsoft Office Suite, and computer-aided design if applicable.
  • Full knowledge of validation and improvement of automated equipment.
  • Ability to troubleshoot manufacturing equipment.
  • Knowledge of material compatibility in the proposed use environment.
  • Ability to understand the fundamentals of project management.
  • Full knowledge of routine preventive maintenance of production equipment.
  • Full knowledge of 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 Practices and Good Documentation Practices supporting a medical-device environment.
  • Strict attention to detail.
  • Must be able to work with other departments, formulate work instructions, and provide guidance and training to lower-level employees with little to no direction.
  • Must adhere to all company rules and requirements, including pandemic protocols and Environmental Health and Safety rules, and take adequate control measures to prevent injuries to themselves and others, protect the environment, and prevent pollution within their span of influence or control.

Responsibilities

  • Troubleshoot and recommend maintenance to limit downtime, keep production on schedule, and ensure ongoing validation compliance.
  • Design, set up, and execute feasibility studies, experiments, and tests by creating and following established protocols to develop findings for validation and improvement of equipment and manufacturing processes or methods based on engineering principles; analyze results, make recommendations, and develop reports for Engineering review.
  • Lead projects related to new equipment validation, equipment investigations, testing, objective evidence of product dispositions, and rework.
  • Perform scheduled and unscheduled preventive maintenance routines on a wider range of complex equipment to validate user operation and avoid program downtime.
  • Check for failures in more complex equipment and processes, perform corrective actions in affected areas experiencing downtime, and conduct and write impact assessment reports of incidents.
  • Collaborate with Quality in devising and implementing corrective actions, exception work orders, Equipment Non-conformance Reports, and Out of Tolerance reports.
  • Review documentation and take appropriate actions to ensure information is appropriately catalogued, follow through to validation and qualification of equipment, and transfer information to appropriate locations, such as Engineering Change Requests, standard operating procedures, drawings, and tooling, for Engineering approval.
  • Use manufacturing software, such as JDE, quality management systems, and product lifecycle management systems, to update documentation.
  • Collaborate with Engineering and computer-aided design or design staff to develop new basic tools.
  • Provide coaching and guidance to technicians.

About the Company

Edwards Lifesciences

Develops transcatheter heart valves and devices

Edwards Lifesciences focuses on cardiovascular medical technologies, especially transcatheter heart valves. Its products enable repairing or replacing diseased heart valves through minimally invasive procedures rather than open-heart surgery. The company builds on a long history that began with the Starr-Edwards valve and now centers on valve therapies and related diagnostics to treat heart disease. It differentiates itself by specializing in valve technologies and transcatheter approaches, backed by a track record of clinical leadership and global reach. The goal is to improve patient outcomes by providing safer, less invasive valve treatment options for people around the world.

Company size
10,001+
Company stage
IPO
Headquarters
Irvine, CA
Founded
1958

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