Date Posted: 06/08/2026
Hiring Organization: Rose International
Position Number: 502451
Industry: Pharmaceutical/Healthcare
Job Title: Operator
Job Location: Westford, MA, USA, 01886
Work Model: Onsite
Shift: 2nd shift Monday - Friday, from 3:30 PM - 2:00 AM.
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 5
Min Hourly Rate($): 20.00
Max Hourly Rate($): 23.00
Must Have Skills/Attributes: Assembly, Production Support
Experience Desired: Experience in a regulated manufacturing or medical device environment (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 Required:
- Assembly, repair, and/or test operations experience (manual dexterity with small components)
- Able to read, comprehend, and follow written procedures and verbal instructions
- Utilize electronic data collection systems and computer software
- Ability to prioritize and sequence work based on precedence and importance
- Ability to make critical decisions and judgments with minimal supervision
- Strong attention to detail and accuracy in record-keeping and documentation
- Ability to maintain accurate travelers and quality documents
Skills Preferred:
- Experience in a medical device or regulated manufacturing environment
- Basic understanding of Lean Manufacturing principles
- Familiarity with Quality Management Systems (QMS) and/or Environmental Management Systems (EMS)
- Experience working in a cleanroom or gowned manufacturing environment
- Strong written and oral communication skills across all levels of an organization
- Experience participating in continuous improvement or quality initiatives
Position Overview:
The company’s AVD Vascular division in Westford, MA is seeking an Operator I for 2nd shift production. This is a non-exempt, light industrial role within a regulated medical device manufacturing environment. The operator will work within a manufacturing cell producing high-quality medical devices, including pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related assemblies. Work is performed under close supervision following standardized procedures, with a strong emphasis on quality, safety, documentation accuracy, and continuous improvement.
Position Responsibilities:
- Perform a combination of assembly, repair, and test operations on pacemakers, ICDs, leads, and related medical device assemblies
- Follow specified and standardized procedures under close and continual supervision
- Ensure job documentation for cell operations is accurate and up to date
- Communicate ideas, problems, and solutions clearly to all levels of manufacturing management in written and oral form
- Maintain a positive attitude with internal and external customers, including during facility tours
- Follow all safety guidelines and utilize appropriate safety devices during all operations
- Participate in continuous improvement and quality initiatives to enhance production processes
- Maintain accurate records to ensure traceability of all parts and timely resolution of quality issues
- Demonstrate a basic understanding of Lean Manufacturing principles
- Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics
- Support divisional initiatives related to Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements - **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.).
I am very happy with the Rose International, and the professionalism of the employees.
Robin, Consultant
I have been very pleased with my experience with Rose International. Everyone that I encountered was very helpful and courteous.
Stephanie, 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
Thanks for the opportunity. If in the future I ever need a job, I would like to work for Rose International.
David, 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
EMPLOYEE COMMENTS