NEW JOB OPENING
LEAD MEDICAL DEVICE ASSEMBLER (R&D)
IN Salt Lake City, UT, USA!

 

Date Posted: 09/24/2026
Hiring Organization: Rose International
Position Number: 508058
Industry: Medical Equipment & Supplies
Job Title: Lead Medical Device Assembler (R&D)
Job Location: Salt Lake City, UT, USA, 84116
Work Model: Onsite
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 13
Min Hourly Rate($): 25.00
Max Hourly Rate($): 35.00
Must Have Skills/Attributes: Manufacturing, Production Support, Troubleshooting
Experience Desired: Experience in a manufacturing environment (5 yrs); Experience operating and troubleshooting production (1 yrs); Experience providing team leadership, training, or work coordination. (1 yrs); Experience in a regulated manufacturing environment, preferably medical devices. (1 yrs); Experience supporting process improvement initiatives. (1 yrs)
Required Minimum Education: High School Diploma or equivalent

**C2C is not available**

 

Job Description
Required Education:

• High School Diploma or Equivalent



Required Skills and Experieince:

• Five or more years of experience in a manufacturing environment.

• Experience operating and troubleshooting production or prototype equipment.

• Experience providing team leadership, training, or work coordination.

• Experience in a regulated manufacturing environment, preferably medical devices.

• Experience supporting process improvement initiatives.

• Ability to read, write, and communicate effectively in English.

• Strong leadership, interpersonal, and communication skills.

• Ability to prioritize and manage multiple tasks while remaining flexible to design and process updates on a regular basis. Ability to lead with some level of ambiguity with a solution-oriented mindset.

• Working knowledge of manufacturing processes and build workflows.

• Ability to operate, troubleshoot, and maintain equipment.

• Strong attention to detail and commitment to quality.

• Effective problem-solving and decision-making skills.

• Proficiency in completing manufacturing and quality documentation accurately.



Lead Medical Device Assembler Responsibilities:

The Lead Assembler is responsible for the fabrication, assembly, testing, and documentation of medical device products. This role serves as a key contact between engineering and other lab assemblers in coordinating resources, schedules, and activities to ensure products are built safely, efficiently, and in compliance with quality requirements. The Lead Assembler provides technical guidance, training, and day-to-day direction to assemblers while helping achieve engineering objectives.



Leadership:

· Provide day-to-day leadership and guidance to assembly personnel, fostering a culture of safety, quality, accountability, and continuous improvement.

· Lead assembly team in a flexible and nimble manner as product design and assembly procedures evolve into their final state.

· Train, mentor, and support assemblers to ensure adherence to established procedures and best practices.

· Assist engineers in coordinating daily work assignments, prioritizing tasks, and resolving issues.

· Promote effective communication and collaboration across assembly and engineering teams.



Process Coordination:

· Coordinate assembly activities to ensure engineering builds are completed on a weekly basis. Ensure manufacturing processes are followed and updated appropriately.

· Communicate build delays, material shortages, equipment concerns, or quality issues to the appropriate engineers.



Technical Operations:

· Set up, operate, adjust, maintain, clean, and troubleshoot manufacturing and prototype equipment.

· Program equipment to perform established routines and processes.

· Coordinate the procurement and availability of materials, components, tooling, and chemicals required for development builds.

· Complete and maintain assembly build records for specified activities.

· Provide technical support and troubleshooting assistance to minimize equipment downtime and maximize productivity.

· Escalate equipment malfunctions or process issues beyond the scope of responsibility to engineering.

· Support the development and implementation of manufacturing process improvements.



Quality & Compliance:

· Perform visual and functional inspections to verify product quality and compliance with established specifications.

· Monitor product quality and initiate corrective actions or escalate concerns when necessary.

· Ensure compliance with all applicable quality system requirements, manufacturing procedures, and regulatory standards.

· Maintain a clean, organized, and inspection-ready work environment.



Reporting & Documentation:

· Complete training documentation and product build documentation accurately and in a timely manner.

· Maintain clear, legible, and complete documentation in accordance with quality system requirements.

· Participate in planning meetings and provide updates on build status, risks, and resource needs.



Other responsibilities of this position include but are not limited to:

· Perform other duties and responsibilities as assigned.

· Adhere to all company safety, environmental, and quality policies and procedures.



Reporting Structure

· Reports directly to the R&D Manager while working closely with manufacturing engineering supervisors on a daily basis.

· This position does not have direct supervisory authority, however strong leadership is required to manage day-to-day activities for assembly team.

· Provides work direction, training, and task coordination for assemblers and supports the engineering supervisor in managing daily build activities.



Physical Requirements

· Occasional lifting of 25-50 pounds and frequent lifting of 10-20 pounds.

· Ability to stand, walk, bend, reach, and perform repetitive motions for extended periods.

· Ability to work with fine motor skills and maintain attention to detail during assembly operations.



Working Conditions

· Lab environments with exposure to moving mechanical equipment, electrical systems, chemicals, solvents, and varying temperatures.

· Required use of personal protective equipment (PPE) and adherence to all safety procedures.

· May involve working with prototype equipment, manufacturing processes, and engineering development activities.

  • **Only those lawfully authorized to work in the designated country associated with the position will be considered.**

  • **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**


 

Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).

 

Apply Now

 

About Rose

  • Founded in 1993
  • Office Locations Across the U.S.
  • 150+ Clients: Corporations and Government Agencies
  • Employee Oriented Company
  • Challenging Assignments Across the U.S.
  • Continuous Professional Development

I am very happy with the Rose International, and the professionalism of the employees.

Robin, Consultant

I believe the best thing that Rose HR has going for it is the incredible responsiveness. Everyone is very quick to reply to any concerns, and contacts the contracted employees very quickly and efficiently.

Kevin, Consultant

Thanks for the opportunity. If in the future I ever need a job, I would like to work for Rose International.

David, Consultant

Rose International was not only attentive and responsive, but they were very professional and helpful whenever I called or needed any assistance.

Diane, Consultant

Rose International maintained good communication during assignments and are very informative through email and phone calls.

Sade, Consultant

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