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Supplier Quality Engineer I, New Product Development

Edwards Lifesciences

Salt Lake City, UT

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JOB DETAILS
SKILLS
Aerospace and Defense, Automotive Industry, CMOS, Catheterization, Contract Manufacturing, Corrective Action, Cross-Functional, Extrusion, Geometric Dimensioning and Tolerancing, Healthcare Providers, Injection Molding, Machining, Manufacturing, Manufacturing/Industrial Processes, Medical Equipment, OEM (Original Equipment Manufacturer), Problem Solving Skills, Procedure Development, Process Capability, Process Validation, Product Development, Product Support, Quality Assurance Methodology, Quality Engineering, Receiving Inspection, Regulations, Research & Development (R&D), Risk Analysis, Risk Management, Root Cause Analysis, Safety Standards, SolidWorks, Statistical Process Control, Strategic Analysis, Test Plan/Schedule, Testing, Vaccination, Vendor/Supplier Evaluation, Vendor/Supplier Management, Vendor/Supplier Selection, Willing to Travel
LOCATION
Salt Lake City, UT
POSTED
30+ days ago
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.


This Supplier Quality Engineer position will play a key role in supporting critical Advanced Catheter projects. This position is cross-functional in nature and requires strong collaboration and partnership with R&D, Design Assurance, Operations, Regulatory Affairs, Supplier Development Engineering and Receiving Inspection. The primary focus of the position is supporting successful part qualification efforts with external suppliers to support product development and commercial launch timelines. The Supplier Quality Engineer will work on-site in a very fast-paced and dynamic environment where being proactive and taking initiative are paramount to success.


How you will make an impact:


+ Facilitate/perform gage studies, process capability studies, and supplier process validations related to critical component features based on risks identified in FMEAs.

+ Develop and validate test methods, which can encompass creating inspection routines on optical measurement equipment and design and creation of inspection fixtures using SolidWorks.

+ Support component and supplier qualification activities from initiation to closure.

+ Supports completion of Design File requirements applicable to supplied components, subassemblies, devices, and services.

+ Create test method procedures and provide engineering support to Receiving Inspection on component test methods and investigations.

+ Support on-site supplier audits.

+ Assess supplier-related non-conformances.

+ Provide support with supplier corrective action requests from initiation to closure.

+ Report on supplier part qualification status at recurring cross-functional project meetings


What you’ll need (Required):


+ Bachelor’s or Master’s degree in Engineering or Scientific field.

+ Must have ability to travel up to 20%.


What else we look for (Preferred):


+ Engineering degree

+ Medical Device, Aerospace, or Automotive industry experience.

+ Experience with either supplier quality, quality engineering, manufacturing, new product development/improvement, or production engineering activities

+ Experience with supplier/vendor management and qualification activities with new suppliers, CMOs (Contract Manufacturing Organizations), or OEMs for new products.

+ Demonstrated experience driving component testing, test method validations, and testing/validating equipment

+ Experience with statistical techniques and tools such as Gage R&R, Statistical Process Control, or Process Capability Studies.

+ In-depth understanding and experience with risk management for validation qualifications (e.g. equipment or process IQ/OQ/PQs).

+ Ability to conduct effective root cause analysis; driving non-conformance investigations; and assessment of corrective action strategies and effectiveness as applied through CAPAs.

+ Knowledge of GD&T and ability to read and interpret drawings.

+ Good understanding of manufacturing processes (i.e., injection molding, extrusion, machining, etc.).


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