Denali Therapeutics Visa Sponsorship USA
Denali Therapeutics is a clinical-stage biopharmaceutical company focused on neurodegenerative diseases. It sponsors a range of visa types, including H-1B and Green Card pathways, making it a viable option for international scientists, researchers, and drug development professionals seeking U.S. work authorization in biotech.
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INTRODUCTION
Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients. We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.
ROLE AND RESPONSIBILITIES
This position is responsible for the strategic and technical leadership of all aspects of Quality Assurance & Quality Control for Denali’s therapeutic products and accountable for the strategic leadership of the function, building & managing appropriate Quality systems and overseeing activities to ensure safe & effective products are delivered to patients.
- Ensure effective and efficient completion of key technical deliverables including Quality Agreements, batch record review, method validation
- Accountable for developing collaborative and productive partnerships across Denali as well as external contract manufacturing organizations, study site pharmacies, and QPs
- Identify & mitigate GMP risks
- Oversee the Quality Management System and modify & develop as needed to meet the growing needs of the organization
- Support investigational new drug applications (IND), ex-US clinical trial applications (CTA), new drug applications (NDA/BLA/MAA) and related correspondence from the US Food and Drug Administration (FDA) and other global regulatory authorities
- Manage internal and external audits
- Partner with external vendors in support of Quality document preparation and submission
- Maintain up-to-date knowledge of the Quality landscape, regulations, and guidelines
- Support development of specifications for biologics and small molecule programs
- Ensure compliance with relevant governing laws, regulations, guidelines, and Denali SOPs
- Lead direct report(s) through annual goal setting, growth planning, adherence to company policies, maintain training compliance and provide ongoing feedback on growth, development and areas of improvement.
BASIC QUALIFICATIONS
- 20+ years relevant experience in GMP Quality or relevant functions, and experience in both biologics and small molecule quality is highly desirable and 15+ years of management experience
- Bachelor’s degree required, and advanced scientific degree desirable
- Broad understanding of international regulations and guidance
- Strong experience in IND and CTA filings. NDA/BLA/MAA experience strongly preferred
- Experience in auditing CMOs and managing internal audits desirable
- Excellent written and verbal communication skills
- Exceptional influencing, partnership, and collaboration skills
- Strong ability to prioritize workload and manage the growth & development of employees
- Well-prepared, competent, and confident when interacting with senior management, health authorities, and internal and external partners
- Able to prospectively identify potential problems and to partner effectively and positively to solve issues
COMPENSATION
- Salary Range: $327,908.00 to $365,929.00. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. This compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future.
Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

INTRODUCTION
Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients. We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.
ROLE AND RESPONSIBILITIES
This position is responsible for the strategic and technical leadership of all aspects of Quality Assurance & Quality Control for Denali’s therapeutic products and accountable for the strategic leadership of the function, building & managing appropriate Quality systems and overseeing activities to ensure safe & effective products are delivered to patients.
- Ensure effective and efficient completion of key technical deliverables including Quality Agreements, batch record review, method validation
- Accountable for developing collaborative and productive partnerships across Denali as well as external contract manufacturing organizations, study site pharmacies, and QPs
- Identify & mitigate GMP risks
- Oversee the Quality Management System and modify & develop as needed to meet the growing needs of the organization
- Support investigational new drug applications (IND), ex-US clinical trial applications (CTA), new drug applications (NDA/BLA/MAA) and related correspondence from the US Food and Drug Administration (FDA) and other global regulatory authorities
- Manage internal and external audits
- Partner with external vendors in support of Quality document preparation and submission
- Maintain up-to-date knowledge of the Quality landscape, regulations, and guidelines
- Support development of specifications for biologics and small molecule programs
- Ensure compliance with relevant governing laws, regulations, guidelines, and Denali SOPs
- Lead direct report(s) through annual goal setting, growth planning, adherence to company policies, maintain training compliance and provide ongoing feedback on growth, development and areas of improvement.
BASIC QUALIFICATIONS
- 20+ years relevant experience in GMP Quality or relevant functions, and experience in both biologics and small molecule quality is highly desirable and 15+ years of management experience
- Bachelor’s degree required, and advanced scientific degree desirable
- Broad understanding of international regulations and guidance
- Strong experience in IND and CTA filings. NDA/BLA/MAA experience strongly preferred
- Experience in auditing CMOs and managing internal audits desirable
- Excellent written and verbal communication skills
- Exceptional influencing, partnership, and collaboration skills
- Strong ability to prioritize workload and manage the growth & development of employees
- Well-prepared, competent, and confident when interacting with senior management, health authorities, and internal and external partners
- Able to prospectively identify potential problems and to partner effectively and positively to solve issues
COMPENSATION
- Salary Range: $327,908.00 to $365,929.00. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. This compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future.
Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.
Job Roles at Denali Therapeutics Companies
How to Get Visa Sponsorship in Denali Therapeutics Visa Sponsorship USA
Target roles aligned with Denali's core research focus
Denali's work centers on neurodegenerative disease research and drug development. Roles in neuroscience, translational medicine, clinical development, and biomarker research are most likely to attract sponsorship consideration from this science-driven organization.
Understand which visa types Denali actively sponsors
Denali sponsors H-1B, TN, J-1, F-1 OPT, F-1 CPT, and Green Card pathways. Knowing which category fits your background before you apply helps you ask informed questions during recruiting conversations and signals genuine preparation to hiring teams.
Prioritize scientific and technical credentials in your application
Biotechnology employers like Denali evaluate candidates on depth of domain expertise. A PhD, postdoc experience, or specialized industry background in areas like protein engineering, neurobiology, or clinical pharmacology will strengthen your sponsorship case significantly.
Research open roles before reaching out to recruiters
Demonstrating specific role awareness during initial contact makes a strong impression at research-focused companies. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history and find Denali openings relevant to your visa type.
Position Green Card sponsorship as a long-term conversation
Denali sponsors EB-2 and EB-3 Green Card pathways for qualifying employees. Rather than leading with this in early interviews, demonstrate your value first, sponsorship for permanent residence is typically discussed after an offer or during onboarding at biotech firms.
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Get Access To All JobsFrequently Asked Questions
Does Denali Therapeutics sponsor H-1B visas?
Yes, Denali Therapeutics sponsors H-1B visas. The company has a track record of supporting international employees through H-1B petitions, particularly for scientific and technical roles in drug discovery, clinical development, and translational research. If you're targeting an H-1B, look for roles in Denali's core research and development functions, where sponsorship need is most consistent.
What visa types does Denali Therapeutics sponsor?
Denali Therapeutics sponsors a range of visa categories including H-1B, TN, J-1, F-1 OPT, F-1 CPT, and Green Card pathways under EB-2 and EB-3 classifications. This breadth makes Denali a practical option for international candidates at various stages of their U.S. work authorization journey, from recent graduates on OPT to experienced professionals pursuing permanent residence.
Which departments or roles at Denali Therapeutics are most likely to receive visa sponsorship?
Sponsorship at Denali is most concentrated in scientific and clinical functions, reflecting the company's focus on neurodegenerative disease research. Roles in neuroscience, translational medicine, biomarker research, clinical pharmacology, protein engineering, and regulatory affairs are strong candidates. Research associate, scientist, and senior scientist titles have historically aligned with the visa types Denali supports.
How do I find open visa-sponsored jobs at Denali Therapeutics?
Migrate Mate is the most direct way to find sponsored roles at Denali Therapeutics. The platform verifies sponsorship history so you're not guessing based on job descriptions that rarely mention visa support explicitly. Filter by company or visa type to surface current Denali openings relevant to your authorization status and background in biotech or pharmaceuticals.
How do I approach the application process at Denali Therapeutics as an international candidate?
Apply through official channels and be transparent about your visa status early in the process. Denali's hiring timelines in biotech can run eight to fourteen weeks from initial screen to offer, so if you're working against an OPT expiration or H-1B cap deadline, communicate that clearly. Tailoring your application to Denali's neuroscience pipeline and demonstrating deep domain expertise will carry more weight than generic sponsorship requests.
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