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 24, 2026. First seen by Alion on Sep 23, 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.
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 employees and manufacturing activities pertaining to the production of products and/or manufacturing processes in - and with manufacturing/technical knowledge of - 1 or more production areas, depending on the complexity of the areas to ensure the specifications and procedures of the company, in addition to conducting performance reviews, including resolving performance issues.
- Oversee the scheduling of work orders and team performance metrics.
- Accountable to ensure staff is appropriately trained to perform assigned work.
- Accountable for productivity and quality metrics of staff and provide regular progress reports and manufacturing metrics to management and cross-functional stakeholders.
- Partner with engineering on investigations and/or corrective actions, perform non-conformance investigations for review with engineering, assures documentation content is valid, may participate in improvement projects including designing, implementing and optimizing procedures and working methods.
- Perform daily audit to ensure employees are in adherence to manufacturing procedures.
- 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 or personnel supervisory in manufacturing areas, working with cross-functional teams, substantial technical knowledge, and experience in related manufacturing, quality and/or product development engineering.
- Experience working in manufacturing process, medical device industry or related industries.
- Intermediate English level.
- Availability to work in Shift A (Monday to Friday 6.00 a.m. to 3.30 p.m)
- Availability to work in La Lima, Cartago
What else we look for (Preferred):
- Proven expertise in Microsoft Office Suite with working knowledge of Enterprise Resource Planning (ERP) system
- Knowledge of lean manufacturing tools.
- Excellent communication and interpersonal relationship skills; possessing strong collaboration skills in partnering with cross functional stakeholders in order to achieve objectives.
- Ability to work in a fast paced, dynamic, and constantly changing work environment.
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