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Senior Manufacturing Engineer

Job in Irvine, Orange County, California, 92713, USA
Listing for: Edwards Lifesciences
Full Time position
Listed on 2026-01-12
Job specializations:
  • Engineering
    Manufacturing Engineer, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 106000 - 149000 USD Yearly USD 106000.00 149000.00 YEAR
Job Description & How to Apply Below

Join to apply for the Senior Manufacturing Engineer role at Edwards Lifesciences

Innovation starts from the heart. At Edwards, we put patients first. We invest a significant proportion of our revenue towards research and development to drive and develop groundbreaking medical innovations for structural heart disease. As part of our New Product Development Engineering team, you will work closely with our R&D and Quality teams to develop the latest tools and technologies to address significant, unmet clinical needs that impact patients’ lives around the world.

Aortic stenosis impacts millions of people globally, yet it often remains under‑diagnosed and under‑treated. Edwards’ groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life‑changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence.

It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

Responsibilities
  • Driving cross-functional coordination to ensure milestones regarding product builds, validations, etc. are met.
  • Direct process development and characterization for Early Human Use, Clinical, and Commercial device releases using DMAIC methodologies.
  • Identifying and ensuring implementation of opportunities to optimize/improve manufacturing processes including using engineering methods (e.g., Six Sigma and Lean methods), employing technical design skills to re‑design/design of and ensuring equipment, tools, fixtures, etc. are up to standards.
  • Developing complex experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyzing results, making recommendations, and developing reports.
  • Developing training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes.
  • Overseeing manufacturing support tasks; giving instruction to technicians on conducting tests; training technicians and providing feedback; and coordinating technician work.
Required Qualifications
  • Bachelor’s Degree in Engineering or a Scientific field with 4 years of experience, either industry or industry/education.
  • Master’s Degree or equivalent in Engineering or a Scientific field with 3 years of experience, either industry or industry/education.
  • Ph.D. or equivalent in Engineering or a Scientific field with industry experience or industry/education.
Preferred Qualifications
  • Proven expertise in the use of MS Office Suite including MS Project; CAD experience preferred.
  • Strong documentation, communication (written and verbal), and interpersonal relationship skills including consultative and relationship management skills.
  • Basic understanding of statistical techniques.
  • Previous experience working with lab/industrial equipment preferred.
  • 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 ability to influence change.
  • 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.
  • Must be able to work in a team environment, including inter‑departmental teams and key contacts representing the organization on contracts or projects.
  • Adheres to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and takes adequate control measures in preventing injuries to themselves and others as well as to the protection of the environment and prevention of pollution under their span of influence/control.

For California, the base pay range for this position is $106,000 to $149,000 (highly experienced).…

Position Requirements
10+ Years work experience
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