NEW JOB OPENING
MEDICAL DEVICE MANUFACTURING TECHNICIAN
IN FREMONT, CA, USA!

 

Date Posted: 10/16/2026
Hiring Organization: Rose International
Position Number: 509361
Industry: Medical Equipment & Supplies
Job Title: Medical Device Manufacturing Technician
Job Location: Fremont, CA, USA, 94538
Work Model: Onsite
Shift: 8:00am to 4:30pm Monday through Friday
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 7
Min Hourly Rate($): 25.50
Max Hourly Rate($): 25.50
Must Have Skills/Attributes: Assembler, Manufacturing, Production Support, Troubleshooting
Experience Desired:
Hands-on experience assembling mechanical & electrical components, and subassemblies (2 yrs),
Experience working in cleanroom manufacturing environments (2 yrs),
Strong ability to read and follow work instructions, manufacturing procedures, & test methods (2 yrs)
Required Minimum Education: High School Diploma or equivalent

**C2C is not available**

 

Job Description
Education:
• High School Diploma or Equivalent

Job Requirements:
• Minimum of 2 years of manufacturing experience.
• Experience assembling mechanical, electrical, or electromechanical products.
• Experience using hand tools, power tools, pneumatic tools, jigs, fixtures, and measuring devices.
• Experience performing assembly, inspection, testing, troubleshooting, repair, and rework of components and finished products.
• Ability to accurately complete electronic manufacturing documentation and production records.
• Experience operating manufacturing equipment and performing machine operation, material handling, packaging, and inspection.
• Ability to monitor production schedules, build rates, and cycle times while meeting productivity goals.
• Experience working with manufacturing systems and basic computer applications.
• Strong attention to detail with a commitment to producing high-quality work.
• Ability to work independently while supporting team objectives.
• Ability to learn and perform multiple manufacturing processes and workstations.
• Experience working in a regulated manufacturing environment (medical device, pharmaceutical, aerospace, electronics, etc.).
• Cleanroom manufacturing experience.
• Experience using microscopes, gauges, calipers, and precision inspection equipment.
• Experience training, coaching, or cross-training manufacturing employees.
• Ability to troubleshoot production issues and support continuous improvement initiatives.
• Experience supporting Lean Manufacturing, operational excellence, or KPI-driven production environments.
• Audit readiness experience in a regulated manufacturing environment.
• Ability to lift up to 50 pounds occasionally and 20 pounds frequently.
• Ability to stand, walk, bend, stoop, kneel, and perform repetitive assembly tasks throughout the workday.
• Manual dexterity to assemble small components and perform precision work.
• Ability to identify defects and color variations during inspection.
• Must be able to wear required PPE and follow all safety and quality procedures.
• Ability to hear and respond to safety alarms and workplace notifications.

Job Summary:
• Assemble mechanical, electrical, and electromechanical components, subassemblies, and finished products in a regulated manufacturing environment.
• Perform product assembly, inspection, testing, troubleshooting, repair, and rework while ensuring compliance with quality and regulatory standards.
• Read and follow manufacturing work instructions, test procedures, engineering documentation, and electronic production records.
• Operate across multiple production workstations and support machine operation, material handling, packaging, and inspection activities.
• Serve as a zone coach by training, mentoring, and supporting team members while helping resolve production issues and improve workflow.
• Monitor production schedules, build rates, cycle times, and daily manufacturing goals to support productivity and on-time delivery.
• Utilize manufacturing systems and computer applications to document production activities, inventory transactions, and quality records.
• Support continuous improvement, Lean Manufacturing, validation activities, and KPI-driven operational excellence initiatives.
• Perform equipment setup, line changeovers, work area preparation, cleanup, and quality checks while maintaining an organized, audit-ready production environment.
• Promote a safe workplace by following all PPE, quality, and regulatory requirements while contributing to overall manufacturing efficiency and product quality.



  • **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

You are customer service oriented. No matter whether it was the Recruiter or someone in Human Resources/Payroll, you were responsive. That to me is key!

Tonya, Consultant

Your team at Rose International is always very helpful and responsive.

Barbara, Consultant

I had a very positive experience working for Rose. The entire process is very efficient and easy.

Joanne, Consultant

It was great working for Rose International. Everyone was extremely helpful.

Rosann, Consultant

Rose International has been great to me. I thank everyone there for all of their hard work; it has not gone unnoticed.

Melody, Consultant

EMPLOYEE COMMENTS

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