Endovascular R&D Sr. Engineer I — Innovate Medical Devices

Merit Medical Systems; South Jordan (UT); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical/Dental & Other Insurances

Onsite clinic

Onsite Cafeterias

3 Weeks' Vacation

Job summary

Merit Medical Systems in South Jordan, UT is seeking a R&D Senior Engineer I (Endovascular) to design, develop and test endovascular devices, including stents, grafts and delivery systems. You’ll contribute to prototypes, ECNs and process improvements, collaborating with manufacturing, quality and regulatory teams.

Expect a full-time, on-site role with day shifts, and opportunities to advance in a growing medical-device environment focused on patient outcomes.

Qualifications

• Bachelor’s degree or higher in engineering or a technical field; six years related experience required
• Master’s degree with four years related experience, or PhD with two years
• Strong analytical and problem-solving skills
• Working knowledge of US and international standards for the department
• Proficient computer skills (spreadsheets, word processing, databases)

Responsibilities

• Design, manufacture, and operation of structures, machines and systems for endovascular projects
• Make decisions on technical problems using advanced techniques and extension of theories
• Supervise technicians or others and collaborate with other engineers
• Write ECNs and create prototypes
• Work on special projects and related duties as required

Skills

Fluoropolymer processing

Stent/Graft/Endoprosthesis

Delivery system manufacturing

Nitinol manufacturing

CoCr manufacturing

Process engineering IQ/OQ/PQ

Education

Bachelor’s degree in Engineering or technical field

Master’s degree in Engineering or technical field

Ph.D. in Engineering or related field

Job description

Merit Medical Systems in South Jordan, UT is seeking a R&D Senior Engineer I (Endovascular) to design, develop and test endovascular devices, including stents, grafts and delivery systems. You’ll contribute to prototypes, ECNs and process improvements, collaborating with manufacturing, quality and regulatory teams.

Expect a full-time, on-site role with day shifts, and opportunities to advance in a growing medical-device environment focused on patient outcomes.