Date Posted: 09/01/2026
Hiring Organization: Rose International
Position Number: 506736
Industry: Pharmaceutical/Healthcare
Job Title: Medical Device Assembler - Cleanroom & Manufacturing
Job Location: Pomona, CA, USA, 91767
Work Model: Onsite
Shift: M-F 6am - 3:30pm
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 7
Min Hourly Rate($): 20.00
Max Hourly Rate($): 20.00
Must Have Skills/Attributes: Assembler, Manufacturing, Warehouse
Experience Desired: Mechanical or medical device assembly experience within a regulated manufacturing environment (1+ yrs); Experience performing repetitive bench assembly, component inspection, line set-up, and clean up (1+ yrs); Familiarity with basic Lean Manufacturing practices, Standard Operating Procedures (1+ yrs); Excellent physical stamina to stand for 8+ hours continuously, perform repetitive push/pull movement (1+ yrs)
Required Minimum Education: High School Diploma or equivalent
**C2C is not available**
Job Description
Required Education:
• High School Diploma
Skills Required:
• 1+ yrs of assembly experience
Physical Requirements:
• Must be physically able to stand for prolonged periods, as this position is not done sitting down
• Candidate may conduct repetitive movements including push/pull moving of product as needed
from the assembly area
• No heavy lifting is required
• Area does require occasional bending, stooping, and movement of
completed product from one area to another, and ability to clean up the manufacturing equipment used
for the area
• Will be standing on feet for entire shift, so comfortable closed-toe shoes are required
Position Overview:
• The Assembler will be responsible for a variety of assembly and non-assembly functions in support of
manufacturing goals
Position Responsibilities:
• Operates equipment used to manufacture products
• Assembles, checks, and inspects products against departmental procedures.
• Responsible for recognizing product or equipment problems that arise during the mfg. process
and escalating to Line Lead or Supervisor
• May be required to assist with the set-up and the clean-up of mfg. equipment
• Active participation in Lean Initiatives
• Works on assignments that are routine in nature, requiring limited judgment
• Responsible for exhibiting professional behavior with both internal/ external business
associates that reflects positively on the company and is consistent with the company’s
policies and practices
• Understands and is aware of the quality consequences which may occur from the improper
performance of their specific job
• Has awareness of device defects that may occur in their area of responsibility, including
product design, verification and validation, manufacturing, and testing activities
• Carries out duties in compliance with established business policies
• Demonstrates commitment to the development, implementation, and effectiveness of Quality
Management System per ISO, FDA, and other regulatory agencies - **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.).
The interactions that I have had with your representatives have always been prompt and very professional. I am very pleased and impressed with your company and services.
Sioe, Consultant
It was great working for Rose International. Everyone was extremely helpful.
Rosann, Consultant
Thanks for the opportunity. If in the future I ever need a job, I would like to work for Rose International.
David, Consultant
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
Each time I contacted Rose, I was completely satisfied with the great attention and customer service I received. Each person was extremely knowledgeable and patient with my concerns or questions.
Diana, Consultant
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