Manufacturing Engineer

Posted 7 Hours Ago
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Irvine, CA, USA
In-Office
69K-98K Annually
Entry level
Healthtech • Pharmaceutical
The Role
The Manufacturing Engineer I will support pilot production, develop manufacturing processes, and drive continuous improvement in a regulated medical device environment.
Summary Generated by Built In

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and delivering lasting solutions for unmet patient needs. Our Manufacturing Engineer I position offers a unique career opportunity to contribute to highly visible products and advance manufacturing excellence.

Imagine how your ideas and expertise can change a patient’s life. Our Manufacturing Engineering – Pilot team plays a critical role in enabling robust, scalable manufacturing processes prior to full commercialization. In this role, you will partner cross‑functionally with Manufacturing, Quality, R&D, and Operations teams to support pilot production, qualify processes and equipment, and drive continuous improvement within a regulated medical device environment.

How You’ll Make an Impact:

  • Contribute as a key member of the Pilot Operations team, supporting programs that advance new medical devices from development through commercialization and scale‑up.

  • Build strong technical and process knowledge to support rapid product development cycles, process stabilization, and successful technology transfer to global manufacturing sites.

  • Develop, implement, and support Manufacturing Execution System (MES) capabilities for products within the Pilot pipeline, ensuring readiness for commercialization and scale.

  • Improve manufacturing processes using engineering methods such as Lean fundamentals and basic statistical analysis to drive continuous improvement.

  • Design, execute, and document experiments and tests, including writing protocols, analyzing results, and developing reports to qualify and validate manufacturing processes.

  • Analyze and help resolve basic manufacturing and compliance issues, including CAPA activities, non‑conformances, and audit observations, in alignment with quality and regulatory requirements.

  • Create and maintain training materials and manufacturing documentation, including work instructions, to support effective knowledge transfer to production teams.

  • Develop and manage project plans using standard project management tools, including timelines and risk analyses, to ensure deliverables meet customer and business expectations.

  • Identify opportunities to redesign basic equipment, tools, fixtures, or processes to improve manufacturing performance, reliability, and scalability.

  • Provide day‑to‑day manufacturing support by guiding technicians through testing activities, training and coaching technicians, providing feedback, and coordinating technician work.

  • Support Pilot Operations leadership with additional responsibilities and tasks as needed to meet evolving business and program needs.

What you’ll need (Required):

  • Bachelor's Degree in Engineering or Scientific field

What Else We Look For (Preferred):

  • Demonstrated proficiency with standard computer tools, including the Microsoft Office Suite (MS Project experience preferred; CAD experience a plus, if applicable).

  • Strong foundational documentation, written and verbal communication, and interpersonal skills.

  • Basic understanding of statistical techniques and their application in manufacturing or engineering environments.

  • Prior experience in Class III medical device manufacturing (preferred).

  • Solid understanding of engineering principles, theories, and concepts relevant to the role.

  • Effective problem‑solving, organizational, analytical, and critical‑thinking skills.

  • Working knowledge of manufacturing processes and equipment used within assigned areas.

  • Knowledge of and adherence to Edwards Environmental Health & Safety (EHS) and Quality guidelines, particularly within regulated cleanroom medical device manufacturing environments.

  • Strong attention to detail and commitment to accuracy.

  • Ability to interact professionally and effectively with employees at all organizational levels.

  • Ability to manage competing priorities in a fast‑paced, dynamic environment.

  • Proven ability to work collaboratively in a team environment, including with supervisors, peers, cross‑functional partners, and external vendors as needed.

  • Ability to build and maintain strong, stable internal working relationships.

  • Commitment to complying with all company policies and requirements, including safety, environmental, quality, and health protocols, and taking appropriate actions to prevent injury, protect the environment, and prevent pollution within their scope of influence.

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $69,000 to $98,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience).  Applications will be accepted while this position is posted on our Careers website.   

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

COVID Vaccination Requirement

Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.

Skills Required

  • Bachelor's Degree in Engineering or Scientific field

Edwards Lifesciences Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Edwards Lifesciences and has not been reviewed or approved by Edwards Lifesciences.

  • Retirement Support Retirement programs include a 401(k) match complemented by a separate profit‑sharing contribution. These elements add meaningful long‑term value to total compensation.
  • Equity Value & Accessibility An employee stock purchase plan with a discount and look‑back feature, alongside stock awards for eligible roles, provides notable upside. Program expansions indicate continued accessibility.
  • Leave & Time Off Breadth Time‑off policies include generous PTO, company holidays, and a year‑end holiday shutdown. These offerings enhance work‑life support when available at the site.

Edwards Lifesciences Insights

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The Company
Draper, Utah
13,687 Employees
Year Founded: 1958

What We Do

Edwards Lifesciences (NYSE: EW), is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. We thrive on discovery and expanding the boundaries of medical technology, serving patients in 100+ countries, with the help of our employees in areas including Clinical Affairs, Quality Engineering, Research & Development, Regulatory Affairs, Sales & Marketing, corporate functions and more. Our roots date back to 1958 when Miles Lowell Edwards, a retired engineer with a background in hydraulics and fuel pump operations, set out to build the first artificial heart. Edwards believed the heart could be mechanized and was encouraged by Dr. Albert Starr to focus on developing an artificial heart valve. After just two years, the first Starr-Edwards mitral valve was developed and successfully placed in a patient. This innovation spawned Edwards Laboratories. Miles’ fascination with healing the heart and helping patients with heart disease stemmed from his own experience with rheumatic fever as a teenager and continues to fuel our patient-first culture today. Today, we are as passionate about providing innovative solutions for people fighting cardiovascular disease as we have ever been. It's our Credo. It takes integrity, collaboration, innovation, and focus. We are leaders in the design and manufacture of tissue replacement heart valves and repair products as well as advanced hemodynamic monitoring. We partner with physicians to innovate products designed to help patients live longer, healthier, and more productive lives. Our work is both rewarding and a privilege. The importance of what we do defines our approach. We work together to create an environment where ideas can flourish and we provide our people with the resources, expertise and support to bring those ideas to life. For our legal terms and trademarks, please visit: https://www.edwards.com/legal/legal-terms

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