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Salary
≈ $50k – $110k per year (Estimated)
Location
In office (Cartago)
Seniority
Junior · 1+ year exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Sep 25, 2026. First seen by Alion on Sep 25, 2026. Edwards Lifesciences scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Edwards Lifesciences is an American medical device company that became independent from Baxter in 2000 but traces its work to the first commercially available artificial heart valve, developed by Miles Lowell Edwards in the late 1950s. It concentrates entirely on structural heart disease and critical care monitoring, and its transcatheter aortic valve replacement business changed cardiac practice by allowing valves to be delivered through a catheter rather than through open chest surgery. Headquartered in Irvine, California and listed on the New York Stock Exchange, it holds a leading position in a market it largely created.

Job 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.

How you’ll make an impact:

  • Supervise trainers, employees and training activities including, but not limited to, management of training materials and inventory, assist with delivery and collection of productivity, quality, and training metrics of staff and trainees, provide regular progress reports and training metrics to management and cross-functional stakeholders, oversee and coach daily execution of trainer methods and tools.
  • Develop, plan, and schedule Screening, Work Trial, and training activities (e.g., training room set-up) in response to Master Product Schedule (MPS) and New Product Introduction (NPI) business needs
  • Provide feedback and/or conduct performance reviews of Trainers and Trainees, including resolving performance issues
  • May participate in improvement projects, partner with engineering on investigations and/or corrective actions, perform non-conformance investigations for review with engineering, assure documentation content is valid
  • Prepare training records to ensure audit compliance
  • Other incidental duties

What you’ll need (Required):

  • Bachelor's Degree in related field (e.g., industrial, chemical, electrical, mechanical, business administration).
  • 1 year of experience leading teams in manufacturing areas, working with cross-functional teams, substantial technical knowledge, and experience in related manufacturing, quality and/or product development engineering. Preferred
  • Experience working in manufacturing process, medical device industry or related industries (electronics, pharmaceutical, food industry or related). Preferred
  • Intermediate English level. Required

Work shift B:

  • Availability to work from Monday to Friday from 2.25 p.m. to 10.25 p.m.

What else we look for (preferred):

  • Substantial technical knowledge, and sufficient experience in related manufacturing, quality and/or product development engineering, with full responsibility for all personnel including hire/fire authority and handling all aspects of employee relations in manufacturing, quality and/or product development engineering.
  • Strong computer skills in Microsoft Office Suite with working knowledge of Enterprise Resource Planning (ERP) system, preferably JDE.
  • Excellent communication and interpersonal relationship skills; possessing strong collaboration skills in partnering with cross functional stakeholders in order to achieve objectives.
  • Full understanding of manufacturing procedures.
  • Ability to supervise/lead employees in a manufacturing environment.
  • Ability to analyze and identify potential line/operation layouts adjustments to improve efficiency.
  • Basic understanding of processes and equipment used in assigned work.
  • Ability to work and excel within a fast paced, dynamic, and constantly changing work environment.
  • Ability to lead teams, provide coaching and feedback, including responsibility for all employee actions including hire/fire authority and partnering with HR on all aspects of employee relations.
  • 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 Lean Manufacturing concepts and Six Sigma
  • Supervise trainers and training support staff, and oversee training function activities.
  • Participate on cross-functional teams (e.g., Engineering, Management, Regulatory, Quality, HR, Planning) for the development of cohesive production operations.
  • May represent the organization to outside contacts, e.g., vendors, suppliers, contractors, staffing agencies
  • 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.
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