Biotech & Pharma STEM OPT Jobs in North Dakota
North Dakota's biotech and pharma sector, anchored by agricultural biotech firms, research institutions, and companies tied to the state's university system in Fargo and Grand Forks, hires international graduates in research, quality, and regulatory roles. F-1 STEM OPT authorization gives eligible graduates up to three years to work for qualifying employers actively filing with OFLC.
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Get Access To All JobsINTRODUCTION
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Aldevron, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you’ll help bring life-changing innovations to life—impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential—one discovery at a time.
Learn about the Danaher Business System which makes everything possible.
ROLE AND RESPONSIBILITIES
The QA Release & Validation Specialist is responsible for reviewing & approving the following:
- Executed batch records & batch disposition
- QC testing assays
- Executed validation documentation
This position reports to the QA Release Supervisor and is part of the QA Release team within the Operational QA organization located in Fargo, ND and will be an on-site role.
In this role, you will have the opportunity to:
- Review production and test records for completeness and accuracy, ensuring data supports release, meets SOP and applicable Regulations, and all deviations have been appropriately investigated and resolved.
- Review Equipment, Process, Computer Validation, and Bioanalytical Method Development Validation executed documentation to ensure compliance with approved protocols, quality standards, and applicable Regulations.
- Serve as the QA subject matter expert and ensure products, testing, and validation activities not meeting specifications are dispositioned appropriately.
BASIC QUALIFICATIONS
The essential requirements of the job include:
- A minimum of one (1) year of experience in a Quality or auditing role
- Experience working in a regulated or GMP-compliant environment.
- Bachelor of Science or life science discipline preferred or equivalent experience.
PREFERRED QUALIFICATIONS
It would be a plus if you also possess previous experience in:
- US Code of Federal Regulations (CFR) and/or EU Regulations
- cGMP
Travel, Motor Vehicle Record & Physical/Environment Requirements:
- No travel is required as this is an on-site position.
- Ability to use computer, monitor, headset, mouse/keyboard, sit/stand desk, and copier/scanner.
- Ability to lift, move or carry equipment up to 50lbs.
COMPENSATION
The annual salary range OR the hourly range for this role is $43,500.00 - $72,000.00 USD. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
INTRODUCTION
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Aldevron, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you’ll help bring life-changing innovations to life—impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential—one discovery at a time.
Learn about the Danaher Business System which makes everything possible.
ROLE AND RESPONSIBILITIES
The QA Release & Validation Specialist is responsible for reviewing & approving the following:
- Executed batch records & batch disposition
- QC testing assays
- Executed validation documentation
This position reports to the QA Release Supervisor and is part of the QA Release team within the Operational QA organization located in Fargo, ND and will be an on-site role.
In this role, you will have the opportunity to:
- Review production and test records for completeness and accuracy, ensuring data supports release, meets SOP and applicable Regulations, and all deviations have been appropriately investigated and resolved.
- Review Equipment, Process, Computer Validation, and Bioanalytical Method Development Validation executed documentation to ensure compliance with approved protocols, quality standards, and applicable Regulations.
- Serve as the QA subject matter expert and ensure products, testing, and validation activities not meeting specifications are dispositioned appropriately.
BASIC QUALIFICATIONS
The essential requirements of the job include:
- A minimum of one (1) year of experience in a Quality or auditing role
- Experience working in a regulated or GMP-compliant environment.
- Bachelor of Science or life science discipline preferred or equivalent experience.
PREFERRED QUALIFICATIONS
It would be a plus if you also possess previous experience in:
- US Code of Federal Regulations (CFR) and/or EU Regulations
- cGMP
Travel, Motor Vehicle Record & Physical/Environment Requirements:
- No travel is required as this is an on-site position.
- Ability to use computer, monitor, headset, mouse/keyboard, sit/stand desk, and copier/scanner.
- Ability to lift, move or carry equipment up to 50lbs.
COMPENSATION
The annual salary range OR the hourly range for this role is $43,500.00 - $72,000.00 USD. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
STEM OPT Biotech & Pharma Job Roles in North Dakota
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Search Biotech & Pharma Jobs in North DakotaBiotech & Pharma STEM OPT Sponsorship Jobs in North Dakota: Frequently Asked Questions
Which biotech & pharma companies sponsor F-1 STEM OPT visas in North Dakota?
North Dakota's biotech sponsorship activity is concentrated among agricultural biotechnology companies, contract research organizations, and firms connected to North Dakota State University and the University of North Dakota research ecosystem. Employers in crop science, fermentation technology, and pharmaceutical manufacturing have filed Labor Condition Applications through OFLC for STEM-eligible roles. Sponsorship volume is smaller than coastal hubs, so filtering by verified filing history is important before applying.
Which cities in North Dakota have the most biotech & pharma F-1 STEM OPT sponsorship jobs?
Fargo leads North Dakota for biotech and pharma hiring, supported by proximity to North Dakota State University and a growing life sciences cluster. Grand Forks follows, driven by University of North Dakota research activity and affiliated spinouts. Bismarck has a smaller but present pharma-adjacent presence tied to healthcare and agricultural chemistry. Most STEM OPT sponsorship opportunities in the state are concentrated in these three cities.
What types of biotech & pharma roles typically qualify for F-1 STEM OPT sponsorship?
Roles that qualify must be tied to a STEM-designated Classification of Instructional Programs code from your degree and require practical application of that training. In biotech and pharma, qualifying positions commonly include research associate, quality control analyst, regulatory affairs specialist, bioinformatics analyst, process development scientist, and laboratory technician roles. The position must be paid, at least part-time, and the employer must be enrolled in E-Verify to participate in the STEM OPT extension program.
How do I find biotech & pharma F-1 STEM OPT sponsorship jobs in North Dakota?
Migrate Mate lets you filter biotech and pharma jobs in North Dakota by employers with verified OFLC filing history, so you can focus on companies that have actively sponsored F-1 workers rather than guessing. This is especially useful in a smaller market like North Dakota, where sponsorship-willing employers are fewer but identifiable. Search by role type, city, and employer to build a targeted list before reaching out.
Are there state-specific or industry-specific considerations for F-1 STEM OPT in North Dakota's biotech sector?
North Dakota's biotech industry leans heavily on agricultural biotechnology and university-affiliated research, which shapes the types of STEM OPT roles available. Employers here may have less institutional experience with F-1 sponsorship than large coastal companies, so it helps to apply to organizations that already have an OFLC filing record. North Dakota State University's International Student Services office is a resource for verifying your STEM OPT eligibility and coordinating with your DSO before starting any role.