Engineer II, Manufacturing

Edwards Lifesciences Gruppe; Draper (UT); On-site; USD 85,000 - 115,000; Full time

Job summary

Edwards Lifesciences in Utah (Draper) is seeking an Engineer II to sustain the THV delivery systems manufacturing and drive continuous improvement initiatives across the production environment. You will collaborate with cross-functional teams to enhance manufacturing processes, improve product quality and reliability, and increase operational efficiency to support business and patient needs.

Responsibilities include process optimization using Six Sigma and LEAN, root cause analysis, designing

Qualifications

• Bachelor’s degree in Engineering or related field with2 years of experience or Master’s degree with internship or senior project in Engineering or related field.
• Experience with reputable regulated manufacturing environments is a plus.
• Experience with RCA, NCRs, and CAPAs is desirable.

Responsibilities

• Optimize manufacturing processes using engineering methods (Six Sigma, LEAN) to improve processes and equipment design.
• Use root cause analysis to solve moderately complex issues.
• Develop experiments and tests to qualify and validate processes; analyze results and report findings.
• Troubleshoot mechanical systems and diagnose inline equipment issues.
• Address moderately complex compliance issues (CAPA, non-conformances, audit observations).
• Create training and work instructions for production to transfer knowledge.
• Create project plans and manage deliverables using project management tools.
• Supervise manufacturing support tasks and coordinate technicians.
• Collaborate with Quality, Complaints, Operations and NPD to solve daily manufacturing problems.

Skills

Lean Six Sigma

LEAN methods

Root Cause Analysis

Project Management

Statistical techniques

CAD

MS Project

Problem-solving

Communication

Education

Bachelor's Degree in Engineering

Master's Degree in Engineering

Tools

MS Project

CAD

Job description

Imagine how your ideas and expertise can change a patient’s life. Our Global Operations & Quality team plays a central part in ensuring our products are delivered to patients with cardiovascular disease. You’ll partner cross-functionally with manufacturing operations and sales teams, delivering thoughtful solutions to complex challenges all while developing your knowledge of the medical device industry. Whether your work includes strategic inventory planning, labeling, warehouse management, material handling, or any of our other supply chain opportunities, you will be making a meaningful contribution to our team and to patients all over 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.

This Engineer II will play a key role in supporting and sustaining the manufacture of THV delivery systems while driving continuous improvement initiatives across the production environment. In collaboration with cross-functional partners, they will identify opportunities to enhance manufacturing processes, improve product quality and reliability, and increase operational efficiency to support business and patient needs.

How you’ll make an impact:

• Optimize manufacturing processes, including using engineering methods (e.g., SIX Sigma and LEAN methods) for continuous process improvement and/or re-design/design of equipment, tools, fixtures, etc. to improve manufacturing processes, employing technical design skills
• Use Root Cause analysis tools to solve moderately complex process issues
• Develop moderately complex experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports
• Troubleshoot simple mechanical systems, and ability to diagnose in-line equipment issues if they arise
• Analyze and resolve moderately complex Compliance issues (e.g., CAPA, non-conformances, audit observations
• Develop training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes
• Establish project plans to ensure deliverables are completed to customer’s expectations, using project management tools (e.g., Project Plan, Risk Analysis, etc.)
• Oversee manufacturing support tasks; give instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work
• Partner with cross-functional groups like Quality, Complaints, Operations and NPD to solve day to day manufacturing problems
• Other incidental duties assigned by Leadership

What you’ll need (Required):

• Bachelor’s Degree in Engineering or Scientific field with 2 years of related experience OR Master’s Degree or equivalent with internship, senior projects, or thesis in Engineering or Scientific field including either industry or industry/education

What else we look for (Preferred):

• Lean Six Sigma certification PMP certification
• Experience working in the medical device industry or another highly regulated manufacturing environment
• Experience with Root Cause Analysis (RCA), Nonconformance Reports (NCRs), and Corrective and Preventive Actions (CAPAs)
• Good computer skills in usage of MS Office Suite including MS Project; CAD experience
• Good documentation, communication (e.g., written and verbal) and interpersonal relationship skills including consultative and relationship management skills
• Basic understanding of statistical techniques
• Solid understanding and knowledge of principles, theories, and concepts relevant to Engineering
• Solid problem-solving, organizational, analytical and critical thinking skills
• Solid understanding of processes and equipment used in assigned work
• 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 the ability to manage vendors and project stakeholders
• 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

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most.