Medtronic
Machine Operator I, Third Shift
- Location
- CT (CT)
- Posted
- Posted yesterday (employer shows the date only)
- Source
- Workday (employer's applicant tracking system)
- Category
- Manufacturing/Quality
- Industry
- Medical Device
Application: Workday — account required, long form — you fill it in on the employer's site.
UNTIL never charges to apply and never asks for payment or personal info on behalf of employers.
From the employer's posting
We anticipate the application window for this opening will close on - 30 Oct 2026
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the Life
The Operator I will support Medtronic's Surgical Innovations Manufacturing Annealing team by operating manufacturing equipment, inspecting monofilament sutures, and performing annealing and winding processes to ensure products meet stringent quality and regulatory standards. This role requires a strong attention to detail, the ability to work with precision equipment and high-powered magnification devices, and a commitment to producing high-quality products that positively impact patient care.
This is a fully onsite position for 3rd shift (Sunday - Thursday - 10:30 PM - 7:00 AM).
Key Responsibilities
- Inspect, anneal, and wind monofilament sutures according to established manufacturing procedures and quality standards.
- Operate light-duty bench and floor-type manufacturing equipment, including winding machines, cutting tools, ovens, and other production equipment.
- Load and unload suture materials into annealing ovens to support the production process.
- Utilize microscopes and other high-powered magnification devices to identify defects and ensure product quality.
- Inspect, wrap, and pull samples of monofilament sutures for testing and verification.
- Operate rotary blades, table cutters, and other cutting equipment to cut sutures to specified lengths.
- Wind suture material from spools onto metal racks in preparation for inspection and cutting operations.
- Verify product quality using prescribed gauges, fixtures, and inspection methods to maintain close tolerances.
- Monitor and document production and quality data in accordance with statistical process control and operational procedures.
- Perform basic machine setup, adjustments, and routine maintenance as needed.
- Troubleshoot process and equipment issues and escalate concerns when appropriate.
- Follow all safety, quality, and regulatory requirements while maintaining a clean and organized work environment.
- Collaborate with engineers, technicians, and team members to improve manufacturing processes and drive continuous improvement initiatives.
Must Have: Required Qualifications
- 0 Years of experience required.
Nice to Have: Preferred Qualifications
- Ability to work in a manufacturing environment and follow detailed work instructions.
- Strong attention to detail and ability to identify product defects.
- Ability to use hand tools, microscopes, and precision measuring devices.
- Basic mechanical aptitude and problem-solving skills.
- Ability to accurately document production and quality information.
- Prior manufacturing, assembly, medical device, or quality inspection experience.
- Experience working with microscopes, magnification equipment, or precision manufacturing processes.
- Knowledge of Good Manufacturing Practices (GMP) and quality systems.
- Experience operating production machinery and performing basic equipment maintenance.
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
…
Similar live roles
- Senior Manufacturing Engineer - Onsite
Medtronic · Posted yesterday
Jacksonville, Florida, United States of America - EHS Specialist
Medtronic · Posted yesterday
Boston, Massachusetts, United States of America - QA Engineer 2
Dexcom · Posted today
San Diego, California - Director, Packaging and Manufacturing Operations
Thermo Fisher Scientific · Posted today
Allentown, Pennsylvania, USA - Senior Clinical Manufacturing Lead II
AbbVie · Posted 1h ago
- Staff OT Manufacturing Engineer- Shockwave
Johnson & Johnson · Posted yesterday
Santa Clara, California, United States of America