Biotech & Pharma H-1B Sponsorship Jobs in South Dakota
H-1B visa sponsorship jobs in South Dakota's biotech and pharma sector are concentrated around Sioux Falls and the research corridors connected to the University of South Dakota and South Dakota State University. Employers like Sanford Health and regional contract research organizations actively hire international talent in research, regulatory, and clinical roles.
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We are seeking a highly motivated Principal Scientist I with extensive AAV gene therapy manufacturing experience to develop state-of-the-art downstream purification processes for next-generation AAV gene therapy. This role is also responsible for executing early-stage process development with the focus on developability of AAV gene therapy lead candidates as well as new platform process development for existing and novel AAV capsids and cargo vectors.
About The Role
Internal Job Title: Principal Scientist I/II
Position Location: Onsite, San Diego, CA
Key Responsibilities
- Lead and manage a 3-5 person downstream process team and provide technical support, training, and SME knowledge to assist with the professional development of direct reports.
- Coordinate activities with associates across upstream process and analytical teams.
- Develop strategies in collaboration with Disease Areas and partner with various line functions to support early drug discovery from target selection and validation through lead compound selection and developability assessment.
- Serve as a subject matter expert to transfer manufacturing process knowledge to Technical Research & Development team and advance pipeline programs into clinical phases.
- Lead effort and work collaboratively with Technical Research & Development to develop innovative and cost-effective downstream processes for next-generation AAV.
- Manage multiple project workflow to ensure timely delivery.
- Prepare written reports conforming to defined documentation practices including electronic lab notebook.
- Other related duties as assigned.
Essential Requirements
- PhD in bioprocessing, biochemical engineering, gene therapy or a related field with 3+ years of relevant process development experience in biotechnology/pharmaceutical environment.
- Experience in people management.
- Knowledge of downstream purification processes including affinity and ion-exchange chromatography with hands-on experience with AKTA purification systems.
- Technical proficiency, creativity, and independent thoughts.
- Effective communication skills to convey scientific concepts to research scientists and cross-functional collaborators.
- Strong organization and problem-solving skills with attention to details.
- Ability to work in a fast-paced and matrix environment.
Desired Requirements
- Experiences in AAV gene therapy.
- Experience with viral gene therapy.
The salary for this position is expected to range between $108,500 and $201,500 per year for Principal Scientist I, and between $119,700 and $222,300 per year for Principal Scientist II. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.
To learn more about the culture, rewards and benefits we offer our people click here.
Why Novartis:
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?
Benefits and Rewards:
Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)
EEO Statement
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
Accessibility & Reasonable Accommodations
The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Summary
We are seeking a highly motivated Principal Scientist I with extensive AAV gene therapy manufacturing experience to develop state-of-the-art downstream purification processes for next-generation AAV gene therapy. This role is also responsible for executing early-stage process development with the focus on developability of AAV gene therapy lead candidates as well as new platform process development for existing and novel AAV capsids and cargo vectors.
About The Role
Internal Job Title: Principal Scientist I/II
Position Location: Onsite, San Diego, CA
Key Responsibilities
- Lead and manage a 3-5 person downstream process team and provide technical support, training, and SME knowledge to assist with the professional development of direct reports.
- Coordinate activities with associates across upstream process and analytical teams.
- Develop strategies in collaboration with Disease Areas and partner with various line functions to support early drug discovery from target selection and validation through lead compound selection and developability assessment.
- Serve as a subject matter expert to transfer manufacturing process knowledge to Technical Research & Development team and advance pipeline programs into clinical phases.
- Lead effort and work collaboratively with Technical Research & Development to develop innovative and cost-effective downstream processes for next-generation AAV.
- Manage multiple project workflow to ensure timely delivery.
- Prepare written reports conforming to defined documentation practices including electronic lab notebook.
- Other related duties as assigned.
Essential Requirements
- PhD in bioprocessing, biochemical engineering, gene therapy or a related field with 3+ years of relevant process development experience in biotechnology/pharmaceutical environment.
- Experience in people management.
- Knowledge of downstream purification processes including affinity and ion-exchange chromatography with hands-on experience with AKTA purification systems.
- Technical proficiency, creativity, and independent thoughts.
- Effective communication skills to convey scientific concepts to research scientists and cross-functional collaborators.
- Strong organization and problem-solving skills with attention to details.
- Ability to work in a fast-paced and matrix environment.
Desired Requirements
- Experiences in AAV gene therapy.
- Experience with viral gene therapy.
The salary for this position is expected to range between $108,500 and $201,500 per year for Principal Scientist I, and between $119,700 and $222,300 per year for Principal Scientist II. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.
To learn more about the culture, rewards and benefits we offer our people click here.
Why Novartis:
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?
Benefits and Rewards:
Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)
EEO Statement
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
Accessibility & Reasonable Accommodations
The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
H-1B Biotech & Pharma Job Roles in South Dakota
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Search Biotech & Pharma Jobs in South DakotaBiotech & Pharma H-1B Sponsorship Jobs in South Dakota: Frequently Asked Questions
Which biotech and pharma companies sponsor H-1B visas in South Dakota?
Sanford Health is among the most active employers sponsoring H-1B visa workers in South Dakota, particularly for research and clinical roles. Regional contract research organizations, agricultural biotech firms tied to South Dakota State University's research programs, and specialty pharmaceutical distributors have also filed H-1B petitions. The state's biotech sector is smaller than coastal hubs, so sponsoring employers tend to be concentrated rather than broadly distributed.
Which cities in South Dakota have the most biotech and pharma H-1B sponsorship jobs?
Sioux Falls accounts for the largest share of biotech and pharma H-1B sponsorship activity in South Dakota, driven by its healthcare and life sciences infrastructure. Brookings is a secondary concentration point, anchored by South Dakota State University's agricultural biotechnology and pharmaceutical sciences programs. Rapid City has a smaller but present life sciences employment base, primarily tied to regional healthcare systems and specialty labs.
What types of biotech and pharma roles typically qualify for H-1B sponsorship in South Dakota?
Roles that qualify for H-1B sponsorship are those classified as specialty occupations, meaning the position normally requires at least a bachelor's degree in a specific field. In biotech and pharma, this includes research scientists, clinical research coordinators, bioinformatics analysts, regulatory affairs specialists, quality assurance managers, and pharmaceutical chemists. Positions requiring a general science background without a degree-specific requirement are less likely to qualify.
How do I find biotech and pharma H-1B sponsorship jobs in South Dakota?
Migrate Mate is built specifically for international job seekers looking for H-1B sponsorship, and you can filter by state and industry to surface biotech and pharma roles in South Dakota directly. Because the state has a smaller life sciences market than coastal regions, filtering by employers with a documented H-1B sponsorship history, as Migrate Mate surfaces, helps you focus on employers already familiar with the process rather than cold-applying broadly.
Are there any state-specific considerations for H-1B sponsorship in South Dakota's biotech and pharma industry?
South Dakota does not have a state income tax, which can affect total compensation comparisons when evaluating offers. The state's biotech sector is closely tied to agricultural science and healthcare rather than traditional pharmaceutical manufacturing, so the types of roles and degree backgrounds in demand differ from states like New Jersey or California. Employers here may have less institutional experience with H-1B petitions, making it worth confirming that a prospective employer has sponsored before.
What is the prevailing wage for H-1B biotech & pharma jobs in South Dakota?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.