Fulgent Therapeutics Visa Sponsorship Jobs USA
Fulgent Therapeutics is a growing player in healthcare and medical services with a track record of sponsoring both H-1B visa and permanent residence visas. For international job seekers targeting clinical, scientific, and technical roles, Fulgent offers a real pathway to U.S. work authorization.
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Fulgent Pharma LLC, a Fulgent Genetics Company, is focused on developing and commercializing innovative anti-cancer therapies that shift the field of cancer treatment toward more effective and more personalized medicine.
Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service genomic testing company built around a foundational technology platform.
Through our diverse testing menu, Fulgent is focused on transforming patient care in oncology, anatomic pathology, infectious and rare diseases, and reproductive health. We believe that by providing a wide range of effective, flexible testing options in conjunction with best-in-class service and support, we can redefine the way medicine is managed for patients and clinicians alike.
As Fulgent's therapeutic development business, Fulgent Pharma LLC, is developing drug candidates for treating a broad range of cancers using a novel nanoencapsulation and targeted therapy platform. By merging Fulgent Genetics and Fulgent Pharma's fields of expertise, we aim to become a fully integrated precision medicine company.
Summary of Position
The Analytical Chemist (Contractor) is to assist the Analytical Director to lead/coordinate the technical and scientific efforts for physical and chemical characterizations using HPLC, GC, SEC, LS, PM, method development, validation, implementation, testing, reporting and method transfer to support pharmaceutical R&D, CMC, and support regulatory filing for drug compounds and formulations.
Key Job Elements
- Independently develops, optimizes, qualifies, validates, troubleshoots, and transfers HPLC/UPLC methods for assay, potency/content, related substances, degradation products, residual free drug, process impurities, formulation components, and stability-indicating applications.
- Executes phase-appropriate analytical method validation activities, including specificity, accuracy, precision, linearity, range, LOD/LOQ, robustness, system suitability, forced degradation, solution stability, and sample stability assessments.
- Performs CMC analytical testing for APIs, polymers/excipients, linkers/payloads where applicable, formulated drug products, and development batches, including release, in-process, characterization, and stability testing.
- Performs or supports additional CMC and physical-chemical testing, which may include GC/residual solvents, SEC, UV/Vis, FTIR, light scattering/particle size, particulate matter/subvisible particles, pH, osmolality, viscosity, appearance, water content, concentration, and formulation performance testing.
- Prepares and reviews analytical protocols, worksheets, raw data packages, method development reports, validation reports, R&D reports, stability summaries, investigation reports, and analytical source documents for CMC sections of IND/NDA or other regulatory submissions.
- Maintains, calibrates, and troubleshoots analytical instruments, especially HPLC/UPLC systems and chromatography data systems; ensures instrument logbooks, preventive maintenance, calibration, reference standards, reagents, columns, and consumables are properly controlled.
- Supports stability programs by coordinating sample pulls, executing testing, trending stability data, evaluating OOT/OOS results, and communicating potential product quality risks in a timely manner.
- Supports CRO/CMO/CDMO analytical activities, including method transfer, technical oversight, protocol/report review, data review, deviation investigation, and communication of analytical requirements for manufacturing and release testing.
- Participates in laboratory investigations, OOS/OOT/deviation assessments, CAPA, change control, data integrity review, and continuous improvement of analytical procedures and laboratory systems.
- Works closely with R&D, manufacturing, quality, regulatory, and operations teams to improve workflow efficiency, documentation quality, testing readiness, and CMC package completeness.
- Adheres to safety and security standards, company policies, applicable SOPs, and laboratory good documentation practices.
- Completes Daily Timesheet accurately and submits as required.
- Performs other duties as assigned, such as assay development, sample management, reference standard coordination, vendor/CRO communication, and drafting technical responses to internal or regulatory questions.
Knowledge/Experience
- Bachelor of Science degree with minimum 6 years of laboratory experience or Master’s Degree with 4 years of laboratory experience or Ph.D. with 2 years of postgraduate research in Chemistry, Biology or related science disciplines.
- Strong hands-on experience with HPLC/UPLC method development, troubleshooting, validation, and routine drug analysis is required.
- Experience independently executing method validation studies and preparing validation protocols/reports for pharmaceutical drug development is strongly preferred.
- Experience with CMC analytical testing for APIs, formulated drug products, impurities/degradants, stability samples, and/or polymer- or nanoparticle-based formulations is preferred.
- Familiarity with cGMP/GLP expectations, good documentation practices, data integrity principles, ICH analytical validation guidance, FDA CMC expectations, and phase-appropriate analytical development practices.
- Experience with instrument maintenance, calibration, and troubleshooting for HPLC/UPLC and other analytical equipment.
- Experience working with CROs/CMOs/CDMOs, method transfer, external data review, and technical communication is preferred.
Additional Skills
- Strong practical knowledge of analytical chemistry, organic chemistry, pharmaceutical analysis, and chromatographic separation principles.
- Ability to independently design experiments, troubleshoot analytical methods, interpret complex chromatograms/data, and recommend scientifically justified next steps.
- Ability to work in a fast-paced small-company environment and prioritize multiple development, stability, and CMC documentation activities.
- Ability to maintain confidentiality, meet deadlines, and follow company SOPs, safety practices, and documentation expectations.
- Preferred experience with oncology drug products, poorly soluble drug formulations, polymer excipients, nanoparticles, ADC-related analytical methods, or a combination of small-molecule and biologics/bioconjugate testing.
Supervisory Responsibilities:
- No direct reports are required for this role. The position may provide technical guidance, training, and day-to-day coordination to junior scientists, analysts, interns, or technicians as assigned.
Reports To:
- Director of Bioanalytical Sciences
Environment
Fulgent Therapeutics LLC is an Equal Employment Opportunity Employer.
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. The term “qualified individual with a disability” means an individual with a disability who, with or without reasonable accommodation, can perform the essential functions of the position.
About us
Fulgent Pharma LLC, a Fulgent Genetics Company, is focused on developing and commercializing innovative anti-cancer therapies that shift the field of cancer treatment toward more effective and more personalized medicine.
Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service genomic testing company built around a foundational technology platform.
Through our diverse testing menu, Fulgent is focused on transforming patient care in oncology, anatomic pathology, infectious and rare diseases, and reproductive health. We believe that by providing a wide range of effective, flexible testing options in conjunction with best-in-class service and support, we can redefine the way medicine is managed for patients and clinicians alike.
As Fulgent's therapeutic development business, Fulgent Pharma LLC, is developing drug candidates for treating a broad range of cancers using a novel nanoencapsulation and targeted therapy platform. By merging Fulgent Genetics and Fulgent Pharma's fields of expertise, we aim to become a fully integrated precision medicine company.
Summary of Position
The Analytical Chemist (Contractor) is to assist the Analytical Director to lead/coordinate the technical and scientific efforts for physical and chemical characterizations using HPLC, GC, SEC, LS, PM, method development, validation, implementation, testing, reporting and method transfer to support pharmaceutical R&D, CMC, and support regulatory filing for drug compounds and formulations.
Key Job Elements
- Independently develops, optimizes, qualifies, validates, troubleshoots, and transfers HPLC/UPLC methods for assay, potency/content, related substances, degradation products, residual free drug, process impurities, formulation components, and stability-indicating applications.
- Executes phase-appropriate analytical method validation activities, including specificity, accuracy, precision, linearity, range, LOD/LOQ, robustness, system suitability, forced degradation, solution stability, and sample stability assessments.
- Performs CMC analytical testing for APIs, polymers/excipients, linkers/payloads where applicable, formulated drug products, and development batches, including release, in-process, characterization, and stability testing.
- Performs or supports additional CMC and physical-chemical testing, which may include GC/residual solvents, SEC, UV/Vis, FTIR, light scattering/particle size, particulate matter/subvisible particles, pH, osmolality, viscosity, appearance, water content, concentration, and formulation performance testing.
- Prepares and reviews analytical protocols, worksheets, raw data packages, method development reports, validation reports, R&D reports, stability summaries, investigation reports, and analytical source documents for CMC sections of IND/NDA or other regulatory submissions.
- Maintains, calibrates, and troubleshoots analytical instruments, especially HPLC/UPLC systems and chromatography data systems; ensures instrument logbooks, preventive maintenance, calibration, reference standards, reagents, columns, and consumables are properly controlled.
- Supports stability programs by coordinating sample pulls, executing testing, trending stability data, evaluating OOT/OOS results, and communicating potential product quality risks in a timely manner.
- Supports CRO/CMO/CDMO analytical activities, including method transfer, technical oversight, protocol/report review, data review, deviation investigation, and communication of analytical requirements for manufacturing and release testing.
- Participates in laboratory investigations, OOS/OOT/deviation assessments, CAPA, change control, data integrity review, and continuous improvement of analytical procedures and laboratory systems.
- Works closely with R&D, manufacturing, quality, regulatory, and operations teams to improve workflow efficiency, documentation quality, testing readiness, and CMC package completeness.
- Adheres to safety and security standards, company policies, applicable SOPs, and laboratory good documentation practices.
- Completes Daily Timesheet accurately and submits as required.
- Performs other duties as assigned, such as assay development, sample management, reference standard coordination, vendor/CRO communication, and drafting technical responses to internal or regulatory questions.
Knowledge/Experience
- Bachelor of Science degree with minimum 6 years of laboratory experience or Master’s Degree with 4 years of laboratory experience or Ph.D. with 2 years of postgraduate research in Chemistry, Biology or related science disciplines.
- Strong hands-on experience with HPLC/UPLC method development, troubleshooting, validation, and routine drug analysis is required.
- Experience independently executing method validation studies and preparing validation protocols/reports for pharmaceutical drug development is strongly preferred.
- Experience with CMC analytical testing for APIs, formulated drug products, impurities/degradants, stability samples, and/or polymer- or nanoparticle-based formulations is preferred.
- Familiarity with cGMP/GLP expectations, good documentation practices, data integrity principles, ICH analytical validation guidance, FDA CMC expectations, and phase-appropriate analytical development practices.
- Experience with instrument maintenance, calibration, and troubleshooting for HPLC/UPLC and other analytical equipment.
- Experience working with CROs/CMOs/CDMOs, method transfer, external data review, and technical communication is preferred.
Additional Skills
- Strong practical knowledge of analytical chemistry, organic chemistry, pharmaceutical analysis, and chromatographic separation principles.
- Ability to independently design experiments, troubleshoot analytical methods, interpret complex chromatograms/data, and recommend scientifically justified next steps.
- Ability to work in a fast-paced small-company environment and prioritize multiple development, stability, and CMC documentation activities.
- Ability to maintain confidentiality, meet deadlines, and follow company SOPs, safety practices, and documentation expectations.
- Preferred experience with oncology drug products, poorly soluble drug formulations, polymer excipients, nanoparticles, ADC-related analytical methods, or a combination of small-molecule and biologics/bioconjugate testing.
Supervisory Responsibilities:
- No direct reports are required for this role. The position may provide technical guidance, training, and day-to-day coordination to junior scientists, analysts, interns, or technicians as assigned.
Reports To:
- Director of Bioanalytical Sciences
Environment
Fulgent Therapeutics LLC is an Equal Employment Opportunity Employer.
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. The term “qualified individual with a disability” means an individual with a disability who, with or without reasonable accommodation, can perform the essential functions of the position.
Job Roles at Fulgent Therapeutics
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Get Access To All JobsTips for Finding Fulgent Therapeutics Visa Sponsorship Jobs USA
Target roles that align with Fulgent's core science
Fulgent's sponsorship activity centers on specialized healthcare and medical services positions. Focus your application on roles in genomics, laboratory science, bioinformatics, or clinical operations where your credentials directly support their work.
Understand which visa types Fulgent supports
Fulgent sponsors both H-1B visas and Green Cards through EB-2 and EB-3 pathways. If long-term U.S. residency is your goal, Fulgent is worth prioritizing, they support candidates through the full immigration journey, not just initial work authorization.
Prepare for a credential-heavy screening process
Healthcare and medical services employers like Fulgent evaluate technical qualifications closely during hiring. Have your degree certificates, transcripts, and any relevant licensure or certifications ready before your first interview to avoid delays.
Apply early relative to the H-1B cap season
H-1B registrations open in March each year. If you're targeting Fulgent for cap-subject sponsorship, aim to have an offer finalized well before February so your employer has time to prepare filings without rushing.
Use a verified sponsor search to find open roles
Not every healthcare company will openly advertise visa sponsorship. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history and confirm Fulgent is actively hiring before investing time in an application.
Highlight specialized skills that are hard to fill domestically
Fulgent, like most healthcare sponsors, pursues sponsorship when a candidate brings skills that are difficult to source locally. Emphasize niche expertise in areas like molecular diagnostics, next-generation sequencing, or clinical data analysis to strengthen your case.
Frequently Asked Questions
Does Fulgent Therapeutics sponsor H-1B visas?
Yes, Fulgent Therapeutics sponsors H-1B visas. The company has a consistent track record of filing H-1B petitions for skilled workers in healthcare and medical services. Roles in laboratory science, bioinformatics, and clinical operations are among the most likely to receive H-1B sponsorship. If you hold a relevant degree in a specialty field, Fulgent is worth targeting during the annual H-1B cap season.
Does Fulgent Therapeutics sponsor Green Cards?
Yes, Fulgent Therapeutics has sponsored permanent residence through both EB-2 and EB-3 classifications. This signals a willingness to invest in long-term immigration support for qualifying employees, not just temporary work authorization. If Green Card sponsorship is a priority for you, it is worth asking directly about their permanent residence policy during the offer stage.
Which roles at Fulgent Therapeutics are most likely to receive visa sponsorship?
Fulgent's sponsorship activity is concentrated in specialized technical and scientific roles that require advanced degrees or highly specific expertise. Positions in genomics, clinical laboratory operations, bioinformatics, software engineering supporting diagnostics, and molecular biology tend to be strong candidates. Roles that require a degree in a defined specialty field are most likely to qualify for H-1B or Green Card sponsorship.
How do I find open visa-sponsored jobs at Fulgent Therapeutics?
Migrate Mate is the most reliable way to find current openings at Fulgent Therapeutics that come with visa sponsorship. The platform verifies sponsorship history so you can confirm Fulgent is actively filing before applying. Filter by company name and visa type to see roles that match your situation, whether you need H-1B cap sponsorship or an employer willing to support a Green Card.
How do I time my application to Fulgent Therapeutics for H-1B sponsorship?
The H-1B cap registration window opens in early March each year, with USCIS selecting registrations by lottery shortly after. To give yourself the best chance, aim to secure an offer from Fulgent by January or February at the latest. That gives both you and the employer enough runway to prepare the petition before the filing deadline. Starting your job search six to nine months before the cap season is a practical approach.