Edwards Lifesciences Corp

Senior Engineer, New Product Introduction

Edwards Lifesciences Corp$108K — $153K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Mechanical, Manufacturing, Industrial Engineering, or related technical field.
  • Minimum 4 years of experience in New Product Introduction (NPI), manufacturing operations, design transfers, or process/equipment validation.
  • Ability to travel up to 20%, including domestically and internationally.
  • Onsite position.

Responsibilities

  • Support operational transitions through development and commercialization phases.
  • Partner with various teams to harmonize transfer plans and validation strategies across manufacturing sites.
  • Lead integration meetings to update stakeholders on progress and risks.
  • Guide the development of supply chain strategies for operational efficiency.
  • Ensure robust characterization and validation in collaboration with R&D and quality partners.
  • Identify manufacturing risks and develop mitigation plans across production sites.
  • Drive continuous improvements in manufacturing processes with a focus on digital and automated solutions.

Benefits

  • Competitive salaries with performance-based incentives.
  • Wide variety of benefits programs to support employees and their families.
Full Job Description
The Senior Engineer, New Product Introduction leads the commercialization of Class III implantable THV products, driving supply chain and manufacturing readiness from early development through product launch. This role partners across R&D, Quality, Supplier Development, and Operations to ensure scalable manufacturing processes, supplier preparedness, and seamless global product delivery, supporting successful product launches across the global supply chain network.

How you'll make an impact:
  • Support operational transitions through development, clinical, and commercialization including completion of design transfer deliverables to ensure end-to-end readiness
  • Partners functionally with pilot, sustaining operations and, domestic and international manufacturing locations to harmonize transfer plans and validation strategies across all sites. Drive line and capacity expansion plans in manufacturing locations in collaboration with demand planning and commercial groups for uninterrupted product supply.
  • Lead critical integration meetings to inform stakeholders across GO&Q and related functions on progress and risks. Ensure risks are clearly identified and addressed for smooth execution of development activities
  • Guide the development of supply chain strategies to attain operational efficiency including assessment of capital and operational expenses to support development needs of the products
  • Ensure development and implementation of robust characterization and validation activities in collaboration with partners from R&D and quality, including deployment of critical control points in manufacturing
  • Identify manufacturing and sale-up risks at pilot and production sites, and develop, implement appropriate mitigation plans, including business continuity plans at suppliers. Ensure clear alignment across sites to harmonize actions and site-to-site transfer of knowledge, process and practices as applicable.
  • Drive continuous improvements in manufacturing processes including opportunities to incorporate digital strategy, automation initiatives, mistake proofing while elevating quality standards
  • Ensures accuracy of part/drawings, bill of materials (BOM) and other manufacturing documentation. Leads the execution of playbooks to ensure successful assessment and deployment of sourcing, planning, transfer and supplier assessment by PDP phases.
  • Ensure design for manufacturability (DFM), Six Sigma, and LEAN considerations are incorporated into product and process designs, including design and process 3P across sites. Support MES deployment as needed
  • Provide analysis and tracks progress against agreed upon targets and deliverables to attain operational metrics required for successful commercialization of products.


What you'll need (Required):
  • Bachelor's degree in Mechanical, Manufacturing, Industrial Engineering, or a related technical field.
  • A minimum of 4 years of experience in NPI/NPD, manufacturing operations, design transfers, and/or process/equipment validation.
  • Ability to travel up to 20%, including domestic and international travel.
  • Onsite position.


What else we look for (Preferred):
  • Understand injection molding, polymers, medical textiles and commonly used materials in the medical device space, such as Nitinol and implantables, with working knowledge of metals processing.
  • Experience in developing process requirement specifications, collaborating with external parties, suppliers and working with Operations personnel to establish efficient solution systems
  • Expertise in the area of manufacturing engineering: design for manufacturability, design and process excellence methodologies including Six Sigma, LEAN experience, cGMP, EH&S guidelines, supplier development engineering and process validation.
  • Excellent communication and interpersonal skills at all levels of employees including upper management, suppliers, operators and external parties.
  • Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making.


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, 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.

About Edwards Lifesciences Corp

Edwards Lifesciences is an American medical technology company headquartered in Irvine, California, specializing in artificial heart valves and hemodynamic monitoring. It developed the SAPIEN transcatheter aortic heart valve made of cow tissue within a balloon-expandable, cobalt-chromium frame, deployed via catheter. The company has manufacturing facilities at the Irvine headquarters, as well as in Draper, Utah; Costa Rica; the Dominican Republic; Puerto Rico; and Singapore; and is building a new facility due to be completed in 2021 in Limerick, Ireland.
Learn more about Edwards Lifesciences Corp
Size
15,700 employees
Market Cap
$45.6 billion
Industry
Net Income
$823.4 million
Founded
1958
5 Year Trend
+12%
Revenue
$4.3 billion
NASDAQ

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