Medical Devices OPT Jobs in South Carolina
South Carolina's medical devices sector spans manufacturing hubs in Greenville, Columbia, and the Upstate region, with companies like Artivion, Teleflex, and Becton Dickinson maintaining operations in the state. F-1 OPT candidates in engineering, quality assurance, and regulatory affairs can find sponsorship-eligible roles with both global manufacturers and regional medical device suppliers.
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Get Access To All JobsINTRODUCTION
SHL Medical is a world-leading provider in the design, development, and manufacturing of advanced self-injection devices. With a global team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, with key operations in Sweden, Taiwan, and the US, we are united by a commitment to innovation, impact, and growth. Together, we empower our people to develop solutions that make a meaningful difference in the lives of millions of patients while fostering a supportive, inclusive, and dynamic workplace for our colleagues.
ROLE AND RESPONSIBILITIES
The Quality Assurance Engineer position would support, oversighting molding production process, launch, scale up, manufacture, and post-market of SHL product to assure SHL quality high standards and compliance with applicable requirements, regulations and SOP’s. Collaborates with regional and global counterparts to ensure consistency of critical processes. Effectively works with local, regional, and global employees to ensure regulatory compliance and SHL standards maintained across different sites.
- Team member representing Quality on product activities, providing quality insight on change control, validation of equipment and processes, and during product life cycle.
- Support the development and launch of new equipment for manufacturing processes.
- Review product performance using statistics tools to identify trends focusing on customer keeping a risk based thinking to prevent quality issues.
- Ensure Non-conformity Material is reviewed and disposed accordingly.
- Partner with Quality Control and manufacturing personnel to confirm failures, and support investigations.
- Establish product inspections processes to assure sampling plans and procedures are aligned to customer’s needs.
- Support test methods development and transfer activities, to ensure those are reproducible by receiving unit.
- Promote the use of statistics and a customer focus approach on product quality and control decisions.
- Review validation protocols and reports to ensure compliance to validation governance documents and GDP requirements.
- Drive Quality Improvement projects and CAPA activities to ensure prevent recurrence of observed or predicted issues and maintain a continuous improvement mentality.
- Support creation of quality engineering procedures, systems and tools and applies them in a dynamic way to development and production projects.
- Collaborate on the review and approval of device master records.
- Technical writing skills for documenting progress, tracking closure of records, and creating training materials.
BASIC QUALIFICATIONS
- 2-5 years of experience in the medical device, pharmaceutical or related regulated industry.
- Knowledge of regulatory compliance: GMP (good manufacturing practice), QSR (quality system regulations), and ISO 13485 is preferred.
- Clear / logical thinking with strong organization and communication skills.
- Risk oriented based thinking.
- Ability to prioritize and to thrive in a cross-functional, inter-company and international environment.
- Team player and self-starter, able to perform with low supervision.
- Experience conducting complex investigations and implementing corrective actions.
- Bachelor’s degree in Life Science, Mechanical Engineering or Engineering discipline.
WHAT WE OFFER
- Competitive compensation package
- Modern working environment with state-of-the-art facilities and technologies
- Challenging assignments in a fast growing and innovative industry
- Position in a dynamic, international team of highly skilled professionals
- Various opportunities for personal and professional development within a global organization
Please note that SHL is a drug free employer. This offer of employment is contingent upon your successful completion of various preemployment screenings, including, but not limited to, a drug test, employment verification, reference checks, and a criminal background check.
INTRODUCTION
SHL Medical is a world-leading provider in the design, development, and manufacturing of advanced self-injection devices. With a global team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, with key operations in Sweden, Taiwan, and the US, we are united by a commitment to innovation, impact, and growth. Together, we empower our people to develop solutions that make a meaningful difference in the lives of millions of patients while fostering a supportive, inclusive, and dynamic workplace for our colleagues.
ROLE AND RESPONSIBILITIES
The Quality Assurance Engineer position would support, oversighting molding production process, launch, scale up, manufacture, and post-market of SHL product to assure SHL quality high standards and compliance with applicable requirements, regulations and SOP’s. Collaborates with regional and global counterparts to ensure consistency of critical processes. Effectively works with local, regional, and global employees to ensure regulatory compliance and SHL standards maintained across different sites.
- Team member representing Quality on product activities, providing quality insight on change control, validation of equipment and processes, and during product life cycle.
- Support the development and launch of new equipment for manufacturing processes.
- Review product performance using statistics tools to identify trends focusing on customer keeping a risk based thinking to prevent quality issues.
- Ensure Non-conformity Material is reviewed and disposed accordingly.
- Partner with Quality Control and manufacturing personnel to confirm failures, and support investigations.
- Establish product inspections processes to assure sampling plans and procedures are aligned to customer’s needs.
- Support test methods development and transfer activities, to ensure those are reproducible by receiving unit.
- Promote the use of statistics and a customer focus approach on product quality and control decisions.
- Review validation protocols and reports to ensure compliance to validation governance documents and GDP requirements.
- Drive Quality Improvement projects and CAPA activities to ensure prevent recurrence of observed or predicted issues and maintain a continuous improvement mentality.
- Support creation of quality engineering procedures, systems and tools and applies them in a dynamic way to development and production projects.
- Collaborate on the review and approval of device master records.
- Technical writing skills for documenting progress, tracking closure of records, and creating training materials.
BASIC QUALIFICATIONS
- 2-5 years of experience in the medical device, pharmaceutical or related regulated industry.
- Knowledge of regulatory compliance: GMP (good manufacturing practice), QSR (quality system regulations), and ISO 13485 is preferred.
- Clear / logical thinking with strong organization and communication skills.
- Risk oriented based thinking.
- Ability to prioritize and to thrive in a cross-functional, inter-company and international environment.
- Team player and self-starter, able to perform with low supervision.
- Experience conducting complex investigations and implementing corrective actions.
- Bachelor’s degree in Life Science, Mechanical Engineering or Engineering discipline.
WHAT WE OFFER
- Competitive compensation package
- Modern working environment with state-of-the-art facilities and technologies
- Challenging assignments in a fast growing and innovative industry
- Position in a dynamic, international team of highly skilled professionals
- Various opportunities for personal and professional development within a global organization
Please note that SHL is a drug free employer. This offer of employment is contingent upon your successful completion of various preemployment screenings, including, but not limited to, a drug test, employment verification, reference checks, and a criminal background check.
OPT Medical Devices Job Roles in South Carolina
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Search Medical Devices Jobs in South CarolinaMedical Devices OPT Sponsorship Jobs in South Carolina: Frequently Asked Questions
Which medical devices companies sponsor F-1 OPT visas in South Carolina?
Companies with medical devices operations in South Carolina that have a track record of sponsoring international candidates include Becton Dickinson, Teleflex, and Artivion. Larger manufacturers with facilities in the Upstate and Midlands regions tend to have established HR processes for OPT and subsequent H-1B visa sponsorship. Smaller contract manufacturers may also sponsor but typically on a case-by-case basis depending on the role and candidate qualifications.
Which cities in South Carolina have the most medical devices F-1 OPT sponsorship jobs?
Greenville and the broader Upstate South Carolina corridor concentrates the largest share of medical devices employment in the state, benefiting from proximity to advanced manufacturing infrastructure. Columbia has a growing life sciences presence supported by the University of South Carolina research ecosystem. Charleston has seen increased medical technology activity tied to its expanding healthcare and biotech sector, making it a secondary market worth tracking.
What types of medical devices roles typically qualify for F-1 OPT sponsorship?
Roles that commonly qualify under F-1 OPT in the medical devices industry include manufacturing engineering, quality engineering, regulatory affairs, R&D, and process validation. These positions typically require a degree in biomedical engineering, mechanical engineering, electrical engineering, or a related field. Positions requiring a direct connection between the job duties and the candidate's field of study are best positioned for OPT authorization and potential STEM OPT extension.
How do I find medical devices F-1 OPT sponsorship jobs in South Carolina?
Migrate Mate is built specifically for international students and filters medical devices jobs in South Carolina by visa sponsorship type, including F-1 OPT. Rather than manually screening hundreds of postings, you can browse roles where employers have indicated sponsorship willingness for OPT candidates. Focusing your search on companies with manufacturing or R&D operations in the Upstate and Columbia areas will give you the most relevant results.
Are there any state-specific or industry-specific considerations for F-1 OPT in South Carolina's medical devices sector?
South Carolina's medical devices manufacturing base leans heavily toward production and quality operations rather than pure research, so roles tied to a STEM degree are common and support STEM OPT extension eligibility for up to 24 additional months. Candidates should confirm their degree program is on the Department of Homeland Security STEM Designated Degree Program List before applying for extension. Employers in regulated medical device environments also frequently require background checks and facility access clearances, which can affect onboarding timelines.