Medical Devices OPT Jobs in Mississippi
Medical devices F-1 OPT sponsorship jobs in Mississippi are concentrated in the Jackson metro area and the Gulf Coast corridor, where manufacturers and distributors with OPT-compatible roles operate. Companies like Hologic, Merit Medical, and regional hospital supply firms have hired OPT candidates in engineering, quality assurance, and regulatory affairs roles.
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Get Access To All JobsPatients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient’s unmet clinical needs. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
How you’ll make an impact:
- Applies professional expertise and judgment to support statistical programming activities and business outcomes.
- Develop complex analysis datasets, specifications, and summary output (tables, listings, or graphs) for inclusion in clinical reports or presentations; Create complex programs that meet regulatory and company standards utilizing statistical programming languages (e.g. SAS, R) to permit efficient programming, reporting, and review.
- Review and validate statistical programs and ensure that all appropriate program documentation and validation meets regulatory and company standards and consistently is structured to permit efficient programming, reporting, and review.
- Perform complex analysis in response to data requests in collaboration with designated statistician.
- Collaborate with CDM (Clinical Data Management) and designated statistician to review draft CRFs (Case Report Forms), database specifications, and perform edit checks.
- Other duties assigned by leadership.
What you’ll need (Required):
- Bachelor's Degree in Statistics, Mathematics, Computer Science or related field, 4 years experience previous statistical programming experience (e.g. SAS) Required or
- Master's Degree or equivalent in Statistics, Mathematics, Computer Science or related field, 2 years experience previous statistical programming experience (e.g. SAS) Required.
What else we look for (Preferred):
- Proven expertise in interfacing MS Office Suite with SAS.
- Good written and verbal communication skills and interpersonal relationship skills including consultative and relationship management skills.
- Full understanding and knowledge relevant to statistical programming.
- Full understanding and knowledge of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/Medical Device setting.
- Strong problem-solving, organizational, analytical and critical thinking skills.
- Experience working in clinical trials within a pharmaceutical/medical device industry.
- Good leadership skills and ability to influence change.
- Strict attention to detail.
- Ability to interact professionally with all organizational levels.
- Ability to manage competing priorities in a fast paced environment.
- Must be able to work in a team environment, including inter-departmental teams and as key contact representing the organization on projects.
- Ability to interact with senior internal and external personnel on significant matters often requiring coordination between organizations.
- Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California, the base pay range for this position is $119,000 - $168,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient’s unmet clinical needs. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
How you’ll make an impact:
- Applies professional expertise and judgment to support statistical programming activities and business outcomes.
- Develop complex analysis datasets, specifications, and summary output (tables, listings, or graphs) for inclusion in clinical reports or presentations; Create complex programs that meet regulatory and company standards utilizing statistical programming languages (e.g. SAS, R) to permit efficient programming, reporting, and review.
- Review and validate statistical programs and ensure that all appropriate program documentation and validation meets regulatory and company standards and consistently is structured to permit efficient programming, reporting, and review.
- Perform complex analysis in response to data requests in collaboration with designated statistician.
- Collaborate with CDM (Clinical Data Management) and designated statistician to review draft CRFs (Case Report Forms), database specifications, and perform edit checks.
- Other duties assigned by leadership.
What you’ll need (Required):
- Bachelor's Degree in Statistics, Mathematics, Computer Science or related field, 4 years experience previous statistical programming experience (e.g. SAS) Required or
- Master's Degree or equivalent in Statistics, Mathematics, Computer Science or related field, 2 years experience previous statistical programming experience (e.g. SAS) Required.
What else we look for (Preferred):
- Proven expertise in interfacing MS Office Suite with SAS.
- Good written and verbal communication skills and interpersonal relationship skills including consultative and relationship management skills.
- Full understanding and knowledge relevant to statistical programming.
- Full understanding and knowledge of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/Medical Device setting.
- Strong problem-solving, organizational, analytical and critical thinking skills.
- Experience working in clinical trials within a pharmaceutical/medical device industry.
- Good leadership skills and ability to influence change.
- Strict attention to detail.
- Ability to interact professionally with all organizational levels.
- Ability to manage competing priorities in a fast paced environment.
- Must be able to work in a team environment, including inter-departmental teams and as key contact representing the organization on projects.
- Ability to interact with senior internal and external personnel on significant matters often requiring coordination between organizations.
- Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California, the base pay range for this position is $119,000 - $168,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
OPT Medical Devices Job Roles in Mississippi
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Search Medical Devices Jobs in MississippiMedical Devices OPT Sponsorship Jobs in Mississippi: Frequently Asked Questions
Which medical devices companies sponsor F-1 OPT visas in Mississippi?
Mississippi's medical devices employers that have supported F-1 OPT candidates include manufacturing subsidiaries, contract research organizations, and hospital supply distributors operating in the Jackson and Gulf Coast areas. Companies involved in orthopedic devices, diagnostics, and surgical instruments tend to have recurring OPT-compatible openings in engineering and quality roles. Checking DOL Labor Condition Application disclosure data can help you identify which specific employers have a history of sponsoring international candidates.
Which cities in Mississippi have the most medical devices F-1 OPT sponsorship jobs?
Jackson is Mississippi's primary hub for medical devices employment, home to hospital systems, device distributors, and biomedical suppliers that recruit OPT candidates. Hattiesburg and Gulfport on the Gulf Coast also have medical manufacturing and healthcare technology operations with OPT-compatible roles. Smaller markets like Tupelo, which has a notable healthcare sector, occasionally post engineering and regulatory positions suited to OPT workers.
What types of medical devices roles typically qualify for F-1 OPT sponsorship?
Roles that commonly qualify include quality engineer, regulatory affairs specialist, biomedical engineer, manufacturing process engineer, R&D technician, and clinical applications specialist. These positions typically require a bachelor's or graduate degree in biomedical engineering, mechanical engineering, biology, or a related field. STEM-designated roles in these categories may also qualify for the 24-month STEM OPT extension if the employer participates in E-Verify and the degree program appears on the STEM OPT eligible programs list.
How do I find medical devices F-1 OPT sponsorship jobs in Mississippi?
Migrate Mate is built specifically for international students and filters medical devices jobs in Mississippi by visa type, showing employers with verified OPT sponsorship history rather than requiring you to cold-screen postings. Beyond Migrate Mate, you can cross-reference DOL OFLC disclosure data to confirm which Mississippi employers have actively supported OPT or H-1B visa filings in medical devices, which signals genuine sponsorship capacity rather than speculative willingness.
Are there state-specific or industry-specific considerations for F-1 OPT in Mississippi's medical devices sector?
Mississippi does not impose state-level work authorization restrictions beyond federal OPT rules, but medical devices roles often carry regulatory compliance requirements that affect hiring timelines. Employers subject to FDA quality system regulations frequently require background checks and onboarding steps that can extend start dates, so coordinating your OPT start date with your employer's onboarding process is important. STEM OPT extensions are available for eligible degree holders if the role and employer meet USCIS and E-Verify requirements.