Date Posted: 10/07/2026
Hiring Organization: Rose International
Position Number: 508826
Industry: Pharmaceutical/Healthcare
Job Title: Medical Device Manufacturing Operator
Job Location: Westford, MA, USA, 01886
Work Model: Onsite
Shift: 5 AM to 3:30 PM (10-hour shift)
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 6
Min Hourly Rate($): 21.50
Max Hourly Rate($): 21.50
Must Have Skills/Attributes: Assembly, Documentation, GMP, Manufacturing, Medical device
Experience Desired:
Experience in medical device, pharmaceutical, electronics, or other highly regulated environments (1-3+ yrs),
Hands-on experience with small-component assembly, catheter assembly, or precision manufacturing (1-3+ yrs),
Experience working under documented procedures and quality requirements (1-3+ yrs)
Required Minimum Education: High School Diploma or equivalent
**C2C is not available**
Job Description
Required Education
• High school diploma or equivalent.
Required Experience
• Manufacturing or assembly experience
• Ability to read, understand, and follow detailed written procedures and verbal instructions.
• Strong attention to detail and commitment to quality.
• Ability to work with small components and perform precision manual assembly.
• Ability to prioritize work and manage multiple production activities.
• Basic computer skills and ability to use electronic data-collection systems.
• Strong communication and teamwork skills.
• Ability to make sound decisions and judgments while working with appropriate supervision.
Preferred Experience
• Medical device manufacturing or assembly experience.
• Catheter or small-component assembly experience.
• Cleanroom or controlled manufacturing experience.
• Pharmaceutical, electronics, semiconductor, or other regulated manufacturing experience.
• Experience with Lean Manufacturing, 5S, continuous improvement, or quality initiatives.
• Experience working with manufacturing travelers, SOPs, quality records, or traceability documentation.
• Familiarity with GMP, ISO, FDA, or other regulated manufacturing requirements.
We are looking for a detail-oriented Medical Device Manufacturing Operator I to join our production team in Westford. In this role, you will manufacture high-quality medical devices and catheter-related assemblies within a controlled manufacturing environment. You will perform precision assembly, repair, testing, documentation, and quality activities while following established procedures and regulatory requirements. This is an excellent opportunity for someone with manufacturing, precision assembly, cleanroom, electronics, pharmaceutical, or medical-device experience who takes pride in producing accurate, high-quality products.
Responsibilities
• Perform assembly, repair, and testing operations on catheters and related medical device assemblies.
• Follow detailed written procedures, work instructions, and verbal directions to complete production activities accurately.
• Maintain accurate manufacturing travelers, quality documentation, production records, and product traceability.
• Inspect work and identify or communicate quality issues so they can be addressed promptly.
• Handle small components and parts requiring precision, consistency, and strong manual dexterity.
• Use electronic data-collection systems and computer software to document production activities.
• Prioritize work based on production requirements, sequencing, timing, and business priorities.
• Follow all safety procedures and use required safety equipment and devices.
• Participate in Lean Manufacturing, continuous improvement, and quality initiatives designed to improve production, quality, and profitability.
• Work with supervisors and managers to support individual goals and manufacturing-cell performance metrics.
• Communicate ideas, problems, and potential solutions clearly to manufacturing leadership and team members.
• Support company Quality Management System (QMS), Environmental Management System (EMS), and other applicable regulatory requirements.
• Maintain a professional and positive attitude when interacting with coworkers, internal customers, and visitors.
Production Environment & Gowning Requirements
This position works in a controlled production environment where strict gowning, cleanliness, safety, and personal-appearance requirements apply. Employees must wear appropriate clean, non-shedding clothing and approved footwear. Certain clothing materials, jewelry, piercings, cosmetics, nail products, fragrances, and other items that could introduce contamination or interfere with production requirements are restricted. - **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.).
Rose International was not only attentive and responsive, but they were very professional and helpful whenever I called or needed any assistance.
Diane, Consultant
My on-boarding with Rose was outstanding. The packets of information, the process, and great attention to detail each person gave me allowed me to get started quickly.I appreciated each person's friendly and helpful attitude.
Diana, Consultant
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
Rose International has been great to me. I thank everyone there for all of their hard work; it has not gone unnoticed.
Melody, Consultant
It was great working for Rose International. Everyone was extremely helpful.
Rosann, Consultant
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