Manager Engineering, NPD Quality

Edwards Lifesciences Corp

Irvine, CA

JOB DETAILS
SALARY
$121,000–$171,000 Per Year
SKILLS
Analysis Skills, Best Practices, Business Skills, Cardiovascular Disease, Catheterization, Clinical Practices/Protocols, Coaching, Communication Skills, Compensation and Benefits, Continuous Improvement, Cross-Functional, Customer Support/Service, Detail Oriented, Documentation, Drug Development, Engineering Management, Environmental Health, FDA (Food and Drug Administration), Failure Mode and Effects Analysis (FMEA), GMP (Good Manufacturing Practices), Healthcare Providers, ISO (International Organization for Standardization), Leadership, Lean Manufacturing, Maintain Compliance, Manufacturing, Manufacturing/Industrial Processes, Medical Equipment, Mentoring, Metrics, Microsoft Office, Operations Planning, Operations Processes, Patient Care, People Management, Pollution Prevention, Problem Solving Skills, Process Capability, Process Improvement, Process Management, Product Development, Product Strategy, Project Execution, Project/Program Management, Quality Engineering, Quality Management, Regulatory Compliance, Regulatory Requirements, Requirements Management, Research & Development (R&D), Risk Management, Safety/Work Safety, Standards Development, Strategic Planning, Team Lead/Manager, Technical Leadership, Technical Presentation, Testing, Time Management, United States Department of Energy (DOE), Usability Engineering, Vaccination, Validation Testing
LOCATION
Irvine, CA
POSTED
4 days ago

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 discovering lasting solutions for unmet patient needs. Our Manager Engineering, NPD Quality, position is a unique career opportunity that could be your next step toward an exciting future.

Imagine how your ideas and expertise can change a patient's life. Our New Product Development Quality team plays a central role in ensuring our innovative products are delivered to patients with cardiovascular disease. You'll partner cross‑functionally with R&D, Manufacturing, Clinical Development, and Regulatory teams, delivering thoughtful solutions to complex challenges while expanding your leadership and knowledge of the medical device industry.

You Will Make an Impact By:

  • Leading quality engineering new product development strategy and execution to ensure compliance with global regulatory requirements and a strong culture of quality
  • Collaborate with global team to support the growth and success of an early-stage innovative product
  • Managing and developing a high-performing team to strengthen business acumen and functional expertise
  • Planning and directing operational and project activities, ensuring successful and timely delivery of key deliverables
  • Driving continuous improvement by identifying opportunities and leading implementation of process enhancements
  • Overseeing engineering activities and providing technical guidance on complex issues and procedures
  • Collaborating cross-functionally across multiple sites and locations as the quality engineering lead for a new product development program, including design, development, characterization, verification, validation, and monitoring
  • Creating and maintaining complex engineering documentation, including design requirements and risk management documents aligned with design control standards
  • Analyzing and resolving complex issues requiring deep technical knowledge
  • Supporting additional duties as needed

What You'll Need (Required):

  • Bachelor's degree in engineering, scientific or related field with related experience in engineering
  • Experience in quality engineering, quality management, and/or regulatory compliance within the medical device industry

What Else We Look For (Preferred):

  • Demonstrating experience within regulated industries and strong knowledge of FDA, GMP, and ISO/EN requirements
  • Experience with product development processes, risk management, and usability engineering.
  • Hands on experience with valve and delivery system, sheath and/or catheter design, manufacturing processes, and testing.
  • Applying advanced statistical and engineering methods, including DOE, SPC, FMEA, process capability, and Lean Manufacturing
  • Leading and developing teams, providing coaching, feedback, and full employee management in partnership with HR
  • Managing technical or engineering functions while mentoring peers and influencing cross-functional partners
  • Driving successful project execution through strong project management and effective use of metrics
  • Applying strong problem-solving, analytical, and critical thinking skills with sound judgment and discretion
  • Communicating effectively, producing high-quality documentation, and building strong stakeholder relationships
  • Defining and standardizing engineering procedures and team operating practices
  • Collaborating with internal teams as well as external suppliers, vendors, and customers
  • Presenting technical information clearly to gain alignment and drive objectives
  • Managing competing priorities and excelling in a fast-paced, dynamic environment
  • Interacting professionally across organizational levels and appropriately escalating issues
  • Using Microsoft Office and related systems with a high level of proficiency
  • Maintaining strong attention to detail and a high standard of quality
  • Building cross-functional relationships to enable best practice sharing and team effectiveness
  • Supporting financial awareness as it relates to quality engineering
  • Delivering proactive, responsive service to meet client and stakeholder needs
  • Adhere to all company rules and requirements (e.g., Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their 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 $121,000 to $171,000 (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.

About the Company

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Edwards Lifesciences Corp