H-1B Visa Pharmaceutical Jobs
Pharmaceutical roles in drug development, regulatory affairs, and clinical research qualify as H-1B visa specialty occupations under USCIS guidelines, requiring at least a bachelor's degree in a directly related field. Large pharma manufacturers, contract research organizations, and biotech firms file H-1B visa petitions regularly, making this one of the more active sectors for visa sponsorship.
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Get Access To All JobsResearch Associate I, Pharmaceutical Development
\~ Contract
Nurix Therapeutics is a biopharmaceutical company focused on the discovery, development, and commercialization of small molecule therapies designed to modulate cellular protein levels as a novel treatment approach for cancer and immune disorders. Leveraging Nurix’s extensive expertise in E3 ligases together with its proprietary DNA-encoded libraries, Nurix has built DELigase, an integrated discovery platform to identify and advance novel drug candidates targeting E3 ligases, a broad class of enzymes that can modulate proteins within the cell. Nurix’s drug discovery approach is to either harness or inhibit the natural function of E3 ligases within the ubiquitin proteasome system to selectively decrease or increase cellular protein levels.
Description
Nurix is looking for a Research Associate I, Pharmaceutical Development to provide scientific, technical, and hands-on support of drug discovery and product development related to small molecules from early discovery to clinical trial enabling studies.
- Prepare and characterize preclinical formulations in support of multiple programs.
- Perform stability and solubility testing using HPLC/UPLC.
- Assist with pre-formulation and formulation development for oral solid dosage forms.
- Contribute to internal and external presentations and publications.
Qualifications
- Thorough understanding of basic chemistry principles
- Excellent basic quantitative laboratory skills including weighing, pipetting, and use of volumetric glassware
- Strong basic HPLC/UPLC skills and understanding (XRD and Mass Spec experience a plus)
- Excellent organizational and documentation skills
- Proficiency in Microsoft 365
- Experience in safe handling of potent compounds
- BS/BA or higher in chemistry, pharmaceutics, engineering, or related field with 2 - 4 years of industry experience
Salary Range: 40/hr - 55/hr
Location: Brisbane, CA - Onsite
Research Associate I, Pharmaceutical Development
\~ Contract
Nurix Therapeutics is a biopharmaceutical company focused on the discovery, development, and commercialization of small molecule therapies designed to modulate cellular protein levels as a novel treatment approach for cancer and immune disorders. Leveraging Nurix’s extensive expertise in E3 ligases together with its proprietary DNA-encoded libraries, Nurix has built DELigase, an integrated discovery platform to identify and advance novel drug candidates targeting E3 ligases, a broad class of enzymes that can modulate proteins within the cell. Nurix’s drug discovery approach is to either harness or inhibit the natural function of E3 ligases within the ubiquitin proteasome system to selectively decrease or increase cellular protein levels.
Description
Nurix is looking for a Research Associate I, Pharmaceutical Development to provide scientific, technical, and hands-on support of drug discovery and product development related to small molecules from early discovery to clinical trial enabling studies.
- Prepare and characterize preclinical formulations in support of multiple programs.
- Perform stability and solubility testing using HPLC/UPLC.
- Assist with pre-formulation and formulation development for oral solid dosage forms.
- Contribute to internal and external presentations and publications.
Qualifications
- Thorough understanding of basic chemistry principles
- Excellent basic quantitative laboratory skills including weighing, pipetting, and use of volumetric glassware
- Strong basic HPLC/UPLC skills and understanding (XRD and Mass Spec experience a plus)
- Excellent organizational and documentation skills
- Proficiency in Microsoft 365
- Experience in safe handling of potent compounds
- BS/BA or higher in chemistry, pharmaceutics, engineering, or related field with 2 - 4 years of industry experience
Salary Range: 40/hr - 55/hr
Location: Brisbane, CA - Onsite
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Get Access To All JobsTips for Finding H-1B Visa Sponsorship in Pharmaceutical
Verify your degree field matches
USCIS requires your degree to directly relate to your pharmaceutical role. A chemistry or pharmacology degree supports a formulation scientist petition, but a general biology degree for a regulatory affairs role can trigger an RFE. Cross-check your transcript against the O*NET occupation profile before applying.
Check LCA filings by occupation code
DOL's OFLC Wage Search lets you filter Labor Condition Applications by Standard Occupational Classification code. Searching SOC 19-1042 (Medical Scientists) or 17-2031 (Biomedical Engineers) shows which employers actively filed for pharmaceutical roles, giving you a verified shortlist of sponsors.
Target employers with DEA registration history
Pharmaceutical companies handling controlled substances must maintain DEA registration, which signals established compliance infrastructure. These organizations tend to have structured immigration programs and in-house counsel familiar with H-1B petitions, reducing the risk of an underprepared sponsor filing your case.
Find verified H-1B pharmaceutical employers on Migrate Mate
Migrate Mate surfaces employers with active H-1B filing history filtered by pharmaceutical occupation codes. You can see which companies have filed LCAs for roles matching your specialty, so you're targeting sponsors with a documented record rather than guessing from job postings.
Negotiate cap-gap protection into your start date
If you're transitioning from F-1 OPT, your cap-gap protection extends work authorization through September 30 after lottery selection. Confirm your offer letter specifies an October 1 start date or later, so your employment aligns with when your H-1B petition becomes effective.
Flag FDA-regulated experience in your petition support letter
Employers filing your I-129 petition should document any FDA submission work, GMP compliance, or IND or NDA contributions in your support letter. USCIS adjudicators are more likely to approve specialty occupation status when your role's regulatory complexity is explicitly tied to your degree requirements.
H-1B Visa Pharmaceutical: Frequently Asked Questions
Do pharmaceutical roles qualify as H-1B specialty occupations?
Yes. Roles in drug development, regulatory affairs, pharmacokinetics, clinical research, and pharmaceutical manufacturing quality typically require at least a bachelor's degree in chemistry, pharmacology, biochemistry, or a closely related field, satisfying the USCIS specialty occupation definition. Generalist roles where any science degree is accepted can face RFEs, so the degree-to-job match matters.
Which types of pharmaceutical employers sponsor H-1B visas most often?
Large integrated pharma manufacturers, contract research organizations, biotech firms, and medical device companies with drug components file the highest volumes of H-1B petitions for pharmaceutical roles. You can identify employers with active H-1B filing history for specific pharmaceutical occupation codes on Migrate Mate, which filters by DOL Labor Condition Application data rather than unverified job postings.
Can I transfer my H-1B to a new pharmaceutical employer mid-visa?
Yes. Under H-1B portability, you can start working for a new pharmaceutical employer as soon as the transfer petition is filed with USCIS, without waiting for approval, provided you're in valid status and the new role is in a specialty occupation. Your new employer files a new I-129, and your existing H-1B validity period carries over.
Does pharmaceutical contract or CRO work affect H-1B sponsorship?
Yes. Contract research organizations sponsor H-1B visas and can place you at a client pharmaceutical site, but USCIS scrutinizes third-party placement petitions closely. The CRO must demonstrate it maintains employer-employee control over your work, including supervision and the right to terminate. Itinerary requirements and end-client letters are standard documentation for these arrangements.
How does the prevailing wage requirement apply to pharmaceutical H-1B roles?
Your employer must pay you at least the DOL prevailing wage for your specific pharmaceutical occupation in the work location's metropolitan area. Wages are determined by your job duties, not your job title, so a regulatory affairs associate doing senior-level work must be paid at the corresponding wage level. You can look up the applicable wage using the OFLC Wage Search by SOC code and location.