Edwards Lifesciences Corp

Senior Engineer, NPD Quality

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

Qualifications

  • Bachelor's or Master's degree in Engineering or a Scientific field with 3-4 years of relevant experience.
  • Proficient in MS Office Suite; CAD experience preferred.
  • Strong documentation and communication skills.
  • Basic understanding of statistical techniques and engineering principles.
  • Leadership skills with the ability to influence change.

Responsibilities

  • Apply quality engineering principles to ensure regulatory compliance for new product development.
  • Develop and maintain design control documentation and design requirement documentation.
  • Update technical content for risk management and usability files.
  • Collaborate across departments to refine processes, drive product testing, and facilitate launches.
  • Investigate complex quality and compliance issues during development, analyzing results and making recommendations.
  • Optimize Manufacturing processes using engineering methods like Six Sigma and Lean.
  • Guide and train technicians in testing procedures, coordinating their work as necessary.

Benefits

  • Competitive salaries with performance-based incentives.
  • Comprehensive benefits programs tailored to individual needs.
  • Opportunity for personal and professional growth in a dynamic environment.
  • Access to cross-functional collaboration and a supportive team culture.
Full Job Description
Senior Engineer, NPD Quality

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

You Will Make an Impact By:
  • Applying knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards systems/procedures for new product development.
  • Developing, updating, and maintaining design control documentation throughout the product development process; supporting the creation of design requirement documentation.
  • Developing, updating, and maintaining the technical content of risk management and usability files.
  • Collaborating with R&D, Manufacturing, and other cross-functional stakeholders to drive process and/or test method development, product builds, clinical programs, design transfer, and product launch; participating in design verification and validation testing.
  • Investigating complex product quality and compliance issues (e.g., pre-commercial complaints, CAPA, non-conformances, audit observations, PRAs) during new product development based on engineering principles; analyzing results, making recommendations, and developing reports.
  • Identifying and ensuring the optimization of complex Manufacturing and/or R&D processes using engineering methods (e.g., Six Sigma, Lean) to support design for manufacturing and continuous process improvement; identifying opportunities for the design or redesign of equipment, tools, fixtures, and related components to improve manufacturing processes and/or test methods and reduce risk.
  • Assigning support tasks and providing instruction to technicians on conducting tests; training technicians and providing feedback; coordinating technician work as needed; and training, coaching, and guiding lower-level employees on routine procedures.
  • Performing other incidental duties as assigned.


What You'll Need (Required):
  • Bachelor's degree in Engineering or a Scientific field and 4 years of related industry experience; OR
  • Master's degree or equivalent in Engineering or a Scientific field and 3 years of related industry or industry/education experience


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 skills.
  • Basic understanding of statistical techniques.
  • Previous experience working with lab/industrial equipment (if applicable).
  • Substantial understanding and knowledge of engineering principles, theories, and concepts relevant to the role.
  • Strong problem-solving, organizational, analytical, and critical-thinking skills.
  • Substantial understanding of the processes and equipment used in assigned work.
  • Good leadership skills and the 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.
  • Ability to work effectively in a team environment, including inter-departmental teams, and to serve as a key contact representing the organization on contracts or projects.
  • Adhere to all company rules and requirements (e.g., pandemic protocols, 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 $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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