Senior Engineer, NPD Manufacturing

Posted 3 Days Ago
Be an Early Applicant
Irvine, CA, USA
In-Office
108K-153K Annually
Senior level
Healthtech • Pharmaceutical
The Role
Provides technical leadership for designing, developing, qualifying, and transferring manufacturing fixtures, tooling, workstations, test systems, and custom equipment for medical device commercialization. Leads mechanical design from concept through production release, improves throughput and equipment effectiveness, troubleshoots manufacturing issues, coordinates suppliers and integrators, and manages verification, validation, documentation, and regulatory compliance.
Summary Generated by Built In

Innovation starts from the heart. Our Advanced Innovation & Technology (AI&T) teams harness the imagination, courage, and resourcefulness to think beyond what’s currently possible, and create solutions for patients many years into the future. If you’re an early-stage innovator, then Edwards AI&T team is the place for you to take the next steps in your career. We’ll give you the tools and resources you need to create groundbreaking innovations that shape the future of structural heart technology.


The Senior NPD Manufacturing Engineer is responsible for providing technical ownership to successfully develop, qualify and transfer manufacturing technologies to commercialize new products in the Advanced Innovation Technology (AI & T) Business Unit. This individual will also advance the objectives of the Global Supply Chain (GSC) by supporting supply chain development and associated engineering activities from early product development through product launch while ensuring that manufacturing processes are developed that fully meet the operational needs for commercial success. The Senior Engineer will work collaboratively with R&D, supplier development, quality, Pilot ops etc., to support product development and deliver on the goals and objectives of the AI&T BU.


How you'll make an impact:


In this role, you will provide technical leadership for the design and development of manufacturing fixtures, tooling, workstations, and custom equipment that enable new product development, commercialization, and production-capacity expansion. This role is centered on hands-on engineering design and equipment development rather than day-to-day line or build management. A major focus will be identifying process bottlenecks and developing new or upgraded equipment that increases throughput, reduces cycle time and manual touch time, improves uptime, and enables scalable manufacturing capacity.


The engineer will translate product, process, user, quality, safety, ergonomic, cycle-time, and capacity requirements into robust mechanical designs, from concepts and 3D CAD models through detailed design, fabrication, assembly, debugging, testing, qualification, installation, and production release. They will work closely with R&D, Quality, Pilot Operations, Supplier Development, Sourcing, Facilities, EH&S, machine shops, equipment integrators, and other Global Supply Chain partners to deliver safe, reliable, maintainable, and compliant manufacturing solutions.


  • Lead the end-to-end mechanical design and development of manufacturing fixtures, tooling, workstations, test systems, and custom equipment for new products, process scale-up, and capacity expansion.
  • Develop new equipment and upgrade existing equipment to eliminate bottlenecks, improve uptime and overall equipment effectiveness, expand output, and support forecasted production-capacity needs without compromising quality or compliance.
  • Develop and compare fixture and equipment concepts using engineering analysis, prototyping, proof-of-concept testing, and risk assessment.
  • Evaluate manual, semi-automated, and automated equipment alternatives, and recommend solutions based on capacity gain, technical feasibility, quality risk, reliability, maintainability, floor-space impact, cost, and implementation complexity.
  • Create and maintain 3D CAD models, detailed drawings, assemblies, bills of materials, design specifications, tolerance analyses and stack-ups, and GD&T documentation for medium- to high-complexity mechanical designs.
  • Apply design for manufacturing and assembly, reliability, maintainability, ergonomics, and EH&S principles throughout the development lifecycle.
  • Perform hands-on troubleshooting and design iteration to resolve mechanical, equipment, process, reliability, usability, and manufacturability issues.
  • Partner with internal machine shops, external fabricators, equipment integrators, and suppliers to support design refinement, component selection, fabrication, assembly, debugging, and commissioning.
  • Lead fixture and equipment characterization, verification, qualification, and validation, including test plans, protocols, acceptance criteria, traceability, and reports.
  • Create and maintain equipment documentation, including specifications, spare-parts recommendations, preventive maintenance requirements, calibration needs, troubleshooting guidance, and training materials.
  • Apply technical principles and Edwards systems and procedures to optimize manufacturing processes, and ensure fixtures, equipment, and documentation comply with applicable quality-system, validation, and regulatory requirements.

What you’ll need (Required):


  • Bachelor's Degree in Engineering or Scientific field with 4 years experience including either industry or industry/education (or)
  • Master's Degree or equivalent in Engineering or Scientific field with 3 years experience including either industry or industry/education (or)
  • Ph.D. or equivalent in Engineering or Scientific field with industry experience or industry/education 

 
What else we look for (Preferred):


  • Proven expertise using the MS Office Suite, including MS Project; CAD experience preferred (if applicable).
  • Strong documentation, communication (written and verbal), and interpersonal relationship skills, including consultative and relationship‑management capabilities.
  • Basic understanding of statistical techniques.
  • Previous experience working with lab or industrial equipment (if applicable).
  • Substantial understanding and knowledge of principles, theories, and concepts relevant to Engineering.
  • Strong problem‑solving, organizational, analytical, and critical‑thinking skills.
  • Substantial understanding of processes and equipment used in assigned work.
  • Good leadership skills and the ability to influence change.
  • Knowledge of and adherence to Edwards Environmental Health & Safety and Quality guidelines as they relate to clean‑room medical device manufacturing.
  • Knowledge of applicable FDA regulations for the medical device industry.
  • Strict attention to detail.
  • Ability to interact professionally with all organizational levels.
  • Ability to manage competing priorities in a fast‑paced environment.
  • Ability to work effectively in a team environment, including inter‑departmental teams, and serve as a key contact representing the organization on contracts or projects.
  • Ability to interact with senior internal and external personnel on significant matters often requiring coordination between organizations.
  • Adherence to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and taking adequate control measures to prevent injuries and environmental harm within one’s span of influence/control.

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 $108,000 to $153,000 (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.

Skills Required

  • Bachelor's degree in Engineering or a scientific field with 4 years of industry or industry/education experience
  • Master's degree or equivalent in Engineering or a scientific field with 3 years of industry or industry/education experience
  • Ph.D. or equivalent in Engineering or a scientific field with industry or industry/education experience
  • Experience using the MS Office Suite, including MS Project
  • CAD experience
  • Strong written, verbal, documentation, communication, and interpersonal skills
  • Basic understanding of statistical techniques
  • Experience working with laboratory or industrial equipment
  • Strong understanding of engineering principles, theories, and concepts
  • Strong problem-solving, organizational, analytical, and critical-thinking skills
  • Understanding of processes and equipment used in assigned work
  • Leadership skills and ability to influence change
  • Knowledge of Environmental Health & Safety and Quality guidelines for clean-room medical device manufacturing
  • Knowledge of applicable FDA regulations for the medical device industry
  • Ability to manage competing priorities in a fast-paced environment
  • Ability to work effectively in cross-functional teams

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.

  • Healthcare Strength — Health coverage is considered strong, with multiple plan choices, HSA options, and fertility support, and the company highlights holistic well‑being programs.
  • Retirement Support — A company 401(k) match and well‑regarded retirement offerings add clear long‑term value to total compensation.
  • Equity Value & Accessibility — An Employee Stock Purchase Plan with a discount and look‑back feature makes equity ownership accessible and enhances the total rewards package.

Edwards Lifesciences Insights

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The Company
HQ: Irvine, CA
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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