Medical Devices STEM OPT Jobs in New Jersey
New Jersey's medical devices industry spans major employers like BD (Becton, Dickinson), Johnson & Johnson MedTech, and Integra LifeSciences, with hiring concentrated in Somerset, Morris, and Middlesex counties. F-1 students in biomedical engineering, electrical engineering, and materials science find STEM OPT-eligible roles across R&D, quality assurance, and regulatory affairs at companies that have established sponsorship track records.
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Get Access To All JobsCompany Description
We are SGS – the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
Job Description
- The Study Manager I, E&L will manage and coordinate projects for extractable and leachable (E&L) testing, including writing and reviewing study protocols and reports.
- Review testing results and compliance with quality criteria in accordance with cGMP. Write/review study reports; Solve questions and comments of the reports from the clients.
- Design the E&L studies and write/review study protocols.
- Work as a technical contact to coordinate extractable and leachable (E&L) projects with clients. Arrange and follow the projects; communicate promptly to solve technical problems as needed.
- Review testing results and compliance with quality criteria in accordance with cGMP. Write/review study reports; Solve questions and comments of the reports from the clients.
- Design the E&L studies and write/review study protocols.
- Work as a technical contact to coordinate extractable and leachable (E&L) projects with clients. Arrange and follow the projects; communicate promptly to solve technical problems as needed.
Qualifications
- Bachelor’s degree in Chemistry or related science.
- 2 years of Extractable and Leachables (E&L) project experience with protocol and report writing experience.
- Knowledge of HPLC/MS and/or GC/MS and/or ICP/MS analytical instrumentation.
- Excellent oral and written communication skills including grammar and composition; Familiar with the common MS Office applications.
- Ability to work well with people of diverse backgrounds.
- Proven project management skills and a strong attention to detail.
- Have excellent interpersonal skills.
- Previous GMP experience.
Additional Information
Our Benefits
We care about your total well-being and will support you with the following, subject to your location and role.
- Health: Medical, dental and vision insurance, life insurance, employee wellness programs.
- Wealth: Competitive pay, 401(k) with company match (immediate vesting upon enrollment), employee referral program, annual bonus target.
- Happiness:
- Professional Growth: Online training courses, virtual and classroom development experiences, tuition reimbursement program.
- Work-Life Balance: Paid-time off (vacation, sick, company holidays, floating holidays, volunteer time).
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company’s rights to assign or reassign duties and responsibilities to this job at any time.
If you are applying for a position within the United States and you have difficulty completing the online employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.
Company Description
We are SGS – the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
Job Description
- The Study Manager I, E&L will manage and coordinate projects for extractable and leachable (E&L) testing, including writing and reviewing study protocols and reports.
- Review testing results and compliance with quality criteria in accordance with cGMP. Write/review study reports; Solve questions and comments of the reports from the clients.
- Design the E&L studies and write/review study protocols.
- Work as a technical contact to coordinate extractable and leachable (E&L) projects with clients. Arrange and follow the projects; communicate promptly to solve technical problems as needed.
- Review testing results and compliance with quality criteria in accordance with cGMP. Write/review study reports; Solve questions and comments of the reports from the clients.
- Design the E&L studies and write/review study protocols.
- Work as a technical contact to coordinate extractable and leachable (E&L) projects with clients. Arrange and follow the projects; communicate promptly to solve technical problems as needed.
Qualifications
- Bachelor’s degree in Chemistry or related science.
- 2 years of Extractable and Leachables (E&L) project experience with protocol and report writing experience.
- Knowledge of HPLC/MS and/or GC/MS and/or ICP/MS analytical instrumentation.
- Excellent oral and written communication skills including grammar and composition; Familiar with the common MS Office applications.
- Ability to work well with people of diverse backgrounds.
- Proven project management skills and a strong attention to detail.
- Have excellent interpersonal skills.
- Previous GMP experience.
Additional Information
Our Benefits
We care about your total well-being and will support you with the following, subject to your location and role.
- Health: Medical, dental and vision insurance, life insurance, employee wellness programs.
- Wealth: Competitive pay, 401(k) with company match (immediate vesting upon enrollment), employee referral program, annual bonus target.
- Happiness:
- Professional Growth: Online training courses, virtual and classroom development experiences, tuition reimbursement program.
- Work-Life Balance: Paid-time off (vacation, sick, company holidays, floating holidays, volunteer time).
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company’s rights to assign or reassign duties and responsibilities to this job at any time.
If you are applying for a position within the United States and you have difficulty completing the online employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.
STEM OPT Medical Devices Job Roles in New Jersey
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Search Medical Devices Jobs in New JerseyMedical Devices STEM OPT Sponsorship Jobs in New Jersey: Frequently Asked Questions
Which medical devices companies in New Jersey sponsor F-1 STEM OPT visas?
New Jersey hosts several medical devices employers with documented STEM OPT hiring activity, including BD (Becton, Dickinson and Company) in Franklin Lakes, Integra LifeSciences in Plainsboro, and Siemens Healthineers' regional operations. Johnson & Johnson MedTech, headquartered in New Brunswick, also has a history of sponsoring international STEM graduates. Larger multinationals in this sector tend to have established HR infrastructure for OPT work authorization verification and E-Verify enrollment, both required for STEM OPT extensions.
Which cities in New Jersey have the most medical devices F-1 STEM OPT sponsorship jobs?
Somerset County and Morris County together account for a large share of New Jersey's medical devices employment, with towns like Franklin Lakes, Parsippany, and Bridgewater hosting major company offices and R&D centers. Middlesex County, including New Brunswick and Plainsboro, is another active cluster. These areas sit along the Route 1 and Route 287 corridors, which have historically attracted life sciences and medtech employers looking for proximity to research universities and pharmaceutical neighbors.
What types of medical devices roles typically qualify for F-1 STEM OPT sponsorship?
Roles in biomedical engineering, electrical engineering, mechanical engineering, quality systems, regulatory affairs, and software development within medical devices companies commonly qualify, provided the position requires a degree in a USCIS-designated STEM field. Research and development positions, manufacturing process engineering, and data science roles tied to device performance or clinical outcomes are frequently listed under qualifying STEM degree classifications. The job offer must align with your designated STEM degree, and your employer must be enrolled in E-Verify before the STEM OPT extension can be authorized by your DSO.
How do I find medical devices F-1 STEM OPT sponsorship jobs in New Jersey?
Migrate Mate lets you filter specifically for medical devices roles in New Jersey that are open to F-1 STEM OPT candidates, showing which employers have active or recent sponsorship history based on DOL filing data. This is more targeted than general job searches because it surfaces companies that have already demonstrated willingness to work with international students. You can narrow results by role type and location within the state, which is useful given how concentrated New Jersey's medtech hiring is in specific counties.
Are there any New Jersey-specific or industry-specific considerations for F-1 STEM OPT sponsorship in medical devices?
New Jersey's medical devices sector operates under FDA regulatory oversight, which means many roles involve quality management systems and documentation standards that require strong technical credentials, often reinforcing why employers seek degreed STEM candidates. The state's proximity to FDA's northeast offices and its dense concentration of life sciences companies means compliance-oriented roles are common. F-1 students should confirm their specific degree program appears on the USCIS STEM Designated Degree Program List and that their employer is E-Verify enrolled before beginning STEM OPT extension paperwork with their DSO.