Imagine how your ideas and expertise can change a patient’s life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You’ll bring your passion for problem solving and partner with various teams to influence decision-making for a product’s entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology.
How you will make an Impact:
- Applies professional expertise and judgment to support product quality activities and business outcomes. Provide clinical expert knowledge and clinical guidance.
- Provide medical/clinical guidance and final direction to complaint staff and engineers related to event interpretation, event investigation, proper coding, required regulatory reporting, and complaint closure.
- Author and/or review complaint conclusions/closure statements and customer communications, including complex or novel cases.
- Evaluate information from clinical specialists, sales staff, physicians, nurses, and other hospital staff/customers, as needed to independently support complaint investigation and drive complex cases towards resolution.
- Evaluate simple and complex imaging such as Echo, Fluoroscopy, CT Scan...related to cardiovascular imaging
- Provide clinical input to Product Risk Assessments and work with Product Safety to support Decision Rationale Matrices, reporting evaluations, and other clinical or patient-risk decisions.
- Develop and deliver clinically based training to complaint staff and engineers on patient anatomy, medical conditions, products, procedures, clinical event interpretation, and applicable internal policies and procedures.
- Review regulatory submissions, regulatory agency requests, or ad hoc clinical analyzes.
- Communicate clinical conclusions, complaint data, trends, and patient-risk information to internal stakeholders in Quality, Manufacturing, Product Safety, and Product Development. Participate as clinical SME in cross-functional discussions and audits, as requested.
- Perform and/or provide clinical interpretation for additional complaint-related clinical activities, which may include review of clinical records, procedural information, literature, images, videos, or other clinical data, based on expertise and business needs.
- Identify and support process improvement opportunities, clinical standardization activities, and development or revision of relevant procedures, tools, and training materials.
- Other incidental duties
What you will need (Required):
- Bachelor's Degree or Equivalent in related field , 5 years’ of previous related experience in a Medical Device Industry, Quality System, hospital/clinical environment (i.e. cardiac care, ICU, OR, or cardiovascular/endovascular interventions)
- Moderate knowledge and understanding of principles, theories, and concepts relevant to cardiovascular imaging
What else we look for (Preferred):
- Digital capabilities (Power BI, Power Automate) and AI knowledge
- Excellent facilitation, presentation, and public speaking skills
Proven successful project management skills - Proven expertise in both Microsoft Office Suite, including advanced Excel and QMS (Quality Management System)
- Excellent documentation and communication skills and interpersonal relationship skills including relationship management skills with ability to drive achievement of objectives
- Recognized as an expert in own area with specialized depth within the organization
- Expert understanding of International Quality System Regulations
Working knowledge of Medical Device regulations, and other applicable regulatory requirements. - Provides consultancy to quality compliance team
- Consult in project setting within specific sections of quality compliance area
- Represents leadership on sections of projects within a specific area interfacing with managers and quality compliance team
- 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
Skills Required
- Bachelor's degree or equivalent in a related field
- Five years of related experience in the medical device industry, quality systems, or a hospital/clinical environment such as cardiac care, ICU, operating room, or cardiovascular/endovascular interventions
- Moderate knowledge of cardiovascular imaging principles, theories, and concepts
- Experience with Power BI and Power Automate
- Knowledge of artificial intelligence
- Excellent facilitation, presentation, and public speaking skills
- Project management experience
- Expertise with Microsoft Office Suite, including advanced Excel
- Experience with Quality Management Systems
- Excellent documentation, communication, interpersonal, and relationship management skills
- Expert understanding of international quality system regulations
- Working knowledge of medical device regulations and other applicable regulatory requirements
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.
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Healthcare Strength — Health coverage is considered strong, with multiple plan choices, HSA options, and fertility support, and the company highlights holistic well‑being programs.
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Retirement Support — A company 401(k) match and well‑regarded retirement offerings add clear long‑term value to total compensation.
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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
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






