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Supplier Quality Engineer

Job in South Jordan, Salt Lake County, Utah, 84095, USA
Listing for: Merit Medical Systems
Full Time position
Listed on 2026-01-07
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, QA Specialist / Manager
  • Engineering
    Quality Engineering, Process Engineer, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.
** WORK SHIFT
** DAY (United States of America)
** SUMMARY OF DUTIES
** This position evaluates the quality and process controls of Merit suppliers; works with them to develop their processes and quality systems to ensure sustainable compliance to the requirements of Merit, customers and industry standards, and assist them in achieving Merit’s quality goals.

ESSENTIAL FUNCTIONS PERFORMED
1.
Maintains the quality performance metrics and requirements for suppliers.  2.
Coordinates the update of Merit documentation to sufficiently describe the products and/or services supplied and the requirements for acceptance.
3.
Maintains the selection, approval and performance evaluation activities needed for suppliers to meet Merit’s specified requirements.  4.
Supports the type and extent of control to be exercised over suppliers based on risk.  5.
Reviews and analyzes data related to supplier approval and performance to specified requirements. Provide reports to management, as appropriate.
6.
Maintains records demonstrating that the specified requirements have been met, including supplier approval, evaluation, audits, corrective and preventative actions.  7.
Facilitates the supplier change notification process to ensure Merit receives advance notification of proposed changes, and approves changes prior to implementation.
8.
Utilizes Supplier Corrective Action Requests to resolve supplier performance problems with Purchasing, Engineering and IQA, as appropriate.  9.
Supports the handling and resolution of supplier related issues using Merit’s risk management process.  10.
Reviews supplier systems and core competencies for gaps that may result in poor quality, including in-process and final inspection processes, and evaluates the need for additional controls at the supplier and Merit to ensure quality levels are maintained or improved.  11.
Coordinates the supplier audit schedule, conducts on-site supplier audits, and evaluates supplier performance.  12.
Reviews Merit’s Receiving Inspection activities/plans for raw components/assemblies/materials purchased from suppliers and associated processes and documentation.  13.
Presents supplier performance metrics and risk updates to management, as required.  14.
Serves as a Merit Quality Liaison for suppliers to ensure effective communication and collaboration between Merit and suppliers.  15.
Performs other related duties and tasks as required.

ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS
• Lifting -- Not to exceed 50 lbs. – local practice may apply.  
• Writing  
• Sitting  
• Standing  
• Bending  
• Vision  
• Color perception  
• Depth perception  
• Reading  
• Field of vision/peripheral  
• Fine motor skills

SUMMARY OF MINIMUM QUALIFICATIONS
• Education and/or experience equivalent to a Bachelor's Degree in Engineering or related field.  
• A minimum of three years of supplier quality and risk management (ISO 14971) experience.  
• Must have knowledge of Quality Engineering discipline, including statistics.  
• Must be able to manage project schedules and timelines in a cross-functional environment.  
• Working knowledge of Lean Manufacturing principles.  
• Ability to understand, analyze, and resolve complex technical problems.  
• Excellent interpersonal, and oral and written communication skills.  
Problem solving and conflict management skills.  
• Excellent organizational skills and the ability to work under strict time constraints.  
• Strong analytical skills and attention to detail.  
• Demonstrated computer skills preferably spreadsheets, word processing, database and other applicable software programs.  
• Required to travel up to 20% of the time.

SUMMARY OF PREFERRED QUALIFICATIONS
• FDA regulated environment experience.  
• Medical instrumentation in a regulated environment (i.e. GMPs, ISO
13485, EN46001, etc.  
• Supplier and part management experience.  
• ASQ Certified Quality Engineer and/or Quality…
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