Medical Devices OPT Jobs in Connecticut
Connecticut's medical devices sector is anchored by companies like Medtronic, Synchronoss, and a dense cluster of device manufacturers along the I-95 and Route 1 corridors. F-1 OPT students in biomedical engineering, quality assurance, and regulatory affairs find active hiring in Milford, Shelton, and the Greater Hartford area, making Connecticut a competitive but opportunity-rich state for medical devices OPT sponsorship.
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We anticipate the application window for this opening will close on - 14 Aug 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
You will be responsible for coordinating the supply of the Hugo™ RAS System with the requisite field resources to ensure a successful integration of a new surgical robot into a hospital. These activities would include working with Field Technical Services to perform a pre-sale site survey, providing simulators for advanced training of surgeons, coordinating schedule for training of surgeons and staff, identifying the Startup Specialist who will support the hospital’s robotic surgery program, identifying the availability date for a robot from the supply chain, and coordinating with Sales to make commitments to customers.
LOCATION: Onsite at North Haven, CT, USA
CONTEXT
You will be a key member of Medtronic’s Global Commercial Enablement team – RST (Robotic Surgical Technologies), working to support the commercialization of our Surgical Robotics Platform in the Americas region. The Americas Installation Planning Manager will be a key member of Commercial Enablement Program Management team in the Robotics Surgical Technologies Business Unit, working to drive successful installation of the Hugo surgical robot and Digital Surgery’s touch surgery platform across sites in Americas. Placement of a surgical robot in a hospital requires coordination of the supply chain with supporting field based resources to ensure successful integration into the hospital’s service lines. This key member will also be an enabler to support installations at clinical trial sites, working closely with customer service, supply chain, field service and various other stakeholders specific to the clinical trials.
Impact patient outcomes. Come for a job, stay for a career.
Medtronic strives to enable earlier diagnosis, better treatment, faster complication-free recovery, and enhanced patient outcomes through less invasive surgical solutions.
The Robotic Surgical Technologies Business Unit set the standard for Robotically Assisted Surgery (RAS) by creating innovative surgical products and services that focus on surgical procedures of diseases and conditions.
MAIN PURPOSE OF JOB
You will be responsible for coordinating the supply of the Hugo™ RAS System with the requisite field resources to ensure a successful integration of a new surgical robot into a hospital. These activities would include working with Field Technical Services to perform a pre-sale site survey, providing simulators for advanced training of surgeons, coordinating schedule for training of surgeons and staff, identifying the Startup Specialist who will support the hospital’s robotic surgery program, identifying the availability date for a robot from the supply chain, and coordinating with Sales to make commitments to customers.
Parallel in preparing for our commercial expansion in the Americas region you will be a Key contributor and leader in all activities around Order to Cash. (Project focused work). This is critical task while we onboard new countries in the region and while we are getting ready to launch the US market.
MAIN JOB DUTIES/RESPONSIBILITIES
- Participate in the Americas sales funnel review process and meet weekly with sales team to review pipeline
- Coordinate with Field Service to perform pre-sale site inspection and track resolution of any findings that would preclude a sale
- Review stocking of consumables and re-usable instruments for accounts in the region
- Determine any pre-sale simulator support requirements
- Obtain assignment of a Startup Specialist to the account
- Ensure the account places an order for consumables and re-usable instruments to support initial use of the system
- Arrange the details of the commissioning including tracking the shipment, notifying Sales, Field Service and the Startup Specialist
- Coordinate with stakeholders for scheduling and managing pre-delivery site inspection, followed-up with successful installation, working in close coordination with Medtronic and customer field team to complete commissioning of Hugo at the hospital
- Coordinate any special requests from the account relative to commissioning
- Maintain metrics and dashboards for process control and transparent communications
- Continuously improve process: Create/follow standard work, define/measure/improve core metrics, develop/utilize global tools, root cause and implement corrective actions for any misses
- Coordinate with clinical research and training (CRMS-PACE) to ensure in-person training is scheduled for surgeons and staff.
- Support import process for certain customers in specific countries within the region by managing clear and accurate documentation readiness
- Ensure deliverables for order entry for transacting Hugo’s capital, consumables and spare parts order codes are tested and active in Medtronic business systems
- Coordinate with global and regional distribution centers for customer order fulfillment of consumables and re-usable instruments
- Lead install management of Hugo at clinical sites in US by coordinating with Medtronic site representative, distribution center, customer service, logistics and project lead
OTC leader/contributor for the Americas region supporting the commercial enablement team in the Region.
Key areas of expertise are:
- Supply chain
- Capital sales
- Order to cash
Project Management
As part of the Surgical Robotics Installation Planning team, you should be able to:
- Work independently, yet in close relationship with its Sales, Customer Training, Field Service, Supply Chain, Customer Service and Robotics Systems Utilization team members
- Communicate clearly and manage expectations in a fast-paced, high stress environment
- Provide hands-on support and also build processes for scaling up
Required Knowledge and Experience: Requires practical knowledge in leading and managing the execution of processes, projects and tactics within one job area.
Typically has advanced knowledge and skills within a specific technical or professional discipline with understanding of the impact of work on other areas of the organization.
Requires a Bachelor's degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) and minimum of 5 years of relevant experience, or advanced degree with a minimum of 3 years of relevant experience.
Preferred Experience:
- Minimum of 5 years in Sales Support, Marketing Support, or Supply Chain planning
- Experience working with cross functional team members
- Experience in outside US markets.
- Fluent in English & Spanish, Knowledge of French or Brazilian Portuguese would be a plus
SKILLS/COMPETENCIES
- Knowledge of supply chain planning, including experience in SAP
- Project planning
- Microsoft Office applications including Word, Excel, and PowerPoint
- Familiar with SFDC
- Strong communication skills
- Presentation skills
PHYSICAL JOB REQUIREMENTS:
Physical capabilities to perform the job:
- 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.
- While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to use a computer and communicate with peers and co-workers via a variety of media including telephone, email, instant message, and in-person meetings.
- This position is based out of North Haven, CT.
WORK ENVIRONMENT:
Office environment where the employee would be standing and sitting most of the day at a desk or in a conference room for meetings.
Travel of less than 25% expected.
The above description is intended to describe the general content, identify the essential functions of, and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements.
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.
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.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD): $120,000.00 - $180,000.00
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others). The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
OPT Medical Devices Job Roles in Connecticut
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Search Medical Devices Jobs in ConnecticutMedical Devices OPT Sponsorship Jobs in Connecticut: Frequently Asked Questions
Which medical devices companies sponsor F-1 OPT visas in Connecticut?
Connecticut hosts several medical devices employers with documented OPT sponsorship activity, including Medtronic, Nuvectra, and Purdue Pharma's device divisions, as well as contract manufacturers and med-tech startups concentrated in the Shelton and Milford corridors. Larger multinational device companies typically have established international student hiring programs, while mid-size manufacturers vary considerably in their willingness to support OPT work authorization.
Which cities in Connecticut have the most medical devices F-1 OPT sponsorship jobs?
Shelton and Milford along the Route 8 and I-95 corridors have the highest concentration of medical devices employers in Connecticut. Greater Hartford, including Farmington and Windsor, also supports device companies tied to the University of Connecticut's biomedical research pipeline. Stamford sees activity from medical technology firms operating near the New York metro boundary, particularly in clinical and regulatory functions.
What types of medical devices roles typically qualify for F-1 OPT sponsorship?
Roles that align directly with STEM degree fields tend to qualify most reliably for OPT work authorization in Connecticut's medical devices sector. Common qualifying positions include quality engineer, regulatory affairs specialist, R&D engineer, manufacturing process engineer, and clinical data analyst. Positions in biomedical engineering, electrical engineering, and applied biology map well to degree requirements that support OPT STEM extension eligibility, which extends authorized work to 24 additional months.
How do I find medical devices F-1 OPT sponsorship jobs in Connecticut?
Migrate Mate filters job listings specifically by visa type and state, making it straightforward to browse medical devices roles in Connecticut that are open to F-1 OPT candidates. Searching on Migrate Mate lets you narrow results to employers who have indicated OPT sponsorship willingness, saving significant time compared to general job searches where visa eligibility is rarely disclosed upfront. Pairing Migrate Mate results with outreach to Connecticut BioScience Growth Council member companies can further expand your pipeline.
Are there any Connecticut-specific or industry-specific considerations for F-1 OPT in medical devices?
Connecticut medical devices employers are subject to FDA regulatory requirements that favor candidates with documented compliance knowledge, which can make STEM OPT students with relevant coursework more competitive. The state's proximity to New York and Massachusetts means many device companies recruit across state lines, so your OPT authorization remains valid regardless of which New England office you work from. Students on STEM OPT extension must also ensure their employer is enrolled in E-Verify, which most established medical devices manufacturers in Connecticut already satisfy.