H-1B Visa Scientist Jobs
Scientist roles qualify for H-1B visa sponsorship when they require at least a bachelor's degree in a directly related field, chemistry, biology, physics, or a related discipline. Many research and industry employers file LCAs through DOL and sponsor H-1B petitions annually. Finding one with active filing history cuts your search time significantly.
Find H-1B Visa Scientist JobsOverview
Showing 5 of 4,191+ Scientist jobs
See all 4,191+ Scientist Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Scientist roles.
Get Access To All JobsThe Role:
Location: Andover, MA
Generate:Biomedicines is seeking an experienced Senior Scientist I to independently lead complex protein production and characterization efforts in support of drug discovery and platform initiatives.
This individual-contributor role will work across upstream construct and expression strategy, mammalian and cell-free protein production, downstream purification, and fit-for-purpose analytical characterization. You will define technical approaches, integrate data across workflows, and make recommendations that enable confident scientific decisions across multiple protein modalities and stages of work.
You will serve as a technical point of contact for protein purification and characterization strategy, partnering with cross-functional teams and external collaborators to align material quality, scale, timelines, and downstream requirements. You will also help advance scalable, data-rich workflows that improve throughput, reproducibility, and organizational learning.
Here's how you will contribute:
- Independently define, plan, and execute complex protein production, purification, and characterization strategies across multiple discovery and platform initiatives. Establish technical milestones, decision criteria, dependencies, and risk-mitigation plans.
- Lead the design, optimization, scale-up, and troubleshooting of protein expression workflows, including transient mammalian and cell-free protein synthesis platforms. Provide technical input into construct design, molecular biology, and stable-expression activities as needed.
- Lead purification workflow development from capture through polishing, with particular emphasis on larger-scale or later-stage protein production. Design and interpret chromatography screening studies, including predictor-plate approaches, resin selection, operating-condition optimization, and scale translation.
- Produce high-quality protein material across a range of formats and scales. Partner with downstream stakeholders to establish fit-for-purpose quality attributes and acceptance criteria based on intended use.
- Select, apply, and interpret appropriate analytical and biochemical characterization methods to assess protein purity, identity, concentration, oligomeric state, aggregation, stability, and other relevant quality attributes.
- Integrate expression, purification, and characterization data to identify root causes, resolve complex technical challenges, evaluate trade-offs, and recommend next steps. Clearly communicate the evidence, assumptions, risks, and uncertainty supporting technical decisions.
- Serve as a technical point of contact for protein production, purification, and characterization strategy. Influence cross-functional decisions by translating scientific findings into clear recommendations for discovery, platform, analytical, and data-focused partners.
- Lead technical interactions with CROs, CDMOs, vendors, and other external partners as appropriate, including defining technical work packages, supporting method or process transfer, reviewing data, troubleshooting issues, and ensuring that deliverables meet scientific requirements.
- Drive the development of scalable, reproducible, and well-documented workflows. Advance the thoughtful use of automation, high-throughput approaches, structured experimental data, and AI/ML-enabled tools to improve scientific productivity and learning.
- Develop and share new methods, technical standards, and best practices. Advise and mentor colleagues, provide constructive scientific feedback, and contribute to an inclusive, collaborative, and high-performing team.
- Demonstrate accountability for scientific quality and delivery by tracking progress, proactively surfacing risks, and communicating successes, setbacks, and lessons learned with clarity and transparency.
The Ideal Candidate will have:
- Independently define, plan, and execute complex protein production, purification, and characterization strategies across multiple discovery and platform initiatives. Establish technical milestones, decision criteria, dependencies, and risk-mitigation plans.
- Lead the design, optimization, scale-up, and troubleshooting of protein expression workflows, including transient mammalian and cell-free protein synthesis platforms. Provide technical input into construct design, molecular biology, and stable-expression activities as needed.
- Lead purification workflow development from capture through polishing, with particular emphasis on larger-scale or later-stage protein production. Design and interpret chromatography screening studies, including predictor-plate approaches, resin selection, operating-condition optimization, and scale translation.
- Produce high-quality protein material across a range of formats and scales. Partner with downstream stakeholders to establish fit-for-purpose quality attributes and acceptance criteria based on intended use.
- Select, apply, and interpret appropriate analytical and biochemical characterization methods to assess protein purity, identity, concentration, oligomeric state, aggregation, stability, and other relevant quality attributes.
- Integrate expression, purification, and characterization data to identify root causes, resolve complex technical challenges, evaluate trade-offs, and recommend next steps. Clearly communicate the evidence, assumptions, risks, and uncertainty supporting technical decisions.
- Serve as a technical point of contact for protein production, purification, and characterization strategy. Influence cross-functional decisions by translating scientific findings into clear recommendations for discovery, platform, analytical, and data-focused partners.
- Lead technical interactions with CROs, CDMOs, vendors, and other external partners as appropriate, including defining technical work packages, supporting method or process transfer, reviewing data, troubleshooting issues, and ensuring that deliverables meet scientific requirements.
- Drive the development of scalable, reproducible, and well-documented workflows. Advance the thoughtful use of automation, high-throughput approaches, structured experimental data, and AI/ML-enabled tools to improve scientific productivity and learning.
- Develop and share new methods, technical standards, and best practices. Advise and mentor colleagues, provide constructive scientific feedback, and contribute to an inclusive, collaborative, and high-performing team.
- Demonstrate accountability for scientific quality and delivery by tracking progress, proactively surfacing risks, and communicating successes, setbacks, and lessons learned with clarity and transparency.
Education and Experience
- Ph.D. in biochemistry, molecular biology, bioengineering, chemical engineering, protein sciences, or a related discipline, with typically 4 or more years of relevant industry experience; or B.S. or M.S. in a relevant scientific or engineering discipline, with typically 12 or more years of relevant industry experience; or an equivalent combination of education and experience that demonstrates the technical depth, independent judgment, and scope of impact required for the role.
Nice to Have
- Experience with stable-expression systems and stable cell-line development activities.
- Experience with construct design, cloning, vector design, or related molecular-biology workflows.
- Experience working with engineered proteins, multispecifics, novel scaffolds, or other complex protein modalities.
- Experience integrating protein design information into expression, purification, or characterization strategies.
- Experience with automation, high-throughput experimentation, laboratory information systems, or structured experimental-data environments.
- Experience managing technical work conducted by CRO, CDMO, or vendor partners.
- Experience developing workflows or methods that were adopted beyond an immediate project or work group.
Who Will Love This Job:
This is an opportunity to shape how Generate produces, characterizes, and learns from protein material in a modern, data-rich discovery environment. Your work will directly influence critical scientific decisions while improving the speed, quality, scale, and reproducibility of workflows used across discovery and platform initiatives.
You will combine hands-on science with meaningful technical ownership, broad cross-functional collaboration, and the opportunity to develop approaches that enable the advancement of next-generation biologics.
About Generate Biomedicines
We are a clinical-stage generative biology company pioneering the AI revolution in drug design and development. We are advancing a new approach to drug creation—one grounded in the ability to design proteins with defined biological intent. By integrating machine learning with large-scale experimentation, this approach aims to reduce the uncertainty, time, and cost associated with developing protein-based medicines.
Founded in 2018, we are advancing a growing pipeline of clinical and preclinical programs across multiple disease areas and protein modalities. By unifying computational design and clinical development within a single operating model, we translate this approach into clinical-stage programs and are leading a shift from traditional drug discovery toward systematic drug generation.
At Generate:Biomedicines, we collaborate across disciplines in new ways to invent and innovate. We bring diverse perspectives to a shared goal of delivering better medicines to patients in need, faster, guided by our values and leadership behaviors.
Generate:Biomedicines is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.
Recruitment & Staffing Agencies: Generate:Biomedicines does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Generate:Biomedicines or its employees is strictly prohibited unless contacted directly by the Company's internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Generate:Biomedicines and the Company will not owe any referral or other fees with respect thereto.
The Role:
Location: Andover, MA
Generate:Biomedicines is seeking an experienced Senior Scientist I to independently lead complex protein production and characterization efforts in support of drug discovery and platform initiatives.
This individual-contributor role will work across upstream construct and expression strategy, mammalian and cell-free protein production, downstream purification, and fit-for-purpose analytical characterization. You will define technical approaches, integrate data across workflows, and make recommendations that enable confident scientific decisions across multiple protein modalities and stages of work.
You will serve as a technical point of contact for protein purification and characterization strategy, partnering with cross-functional teams and external collaborators to align material quality, scale, timelines, and downstream requirements. You will also help advance scalable, data-rich workflows that improve throughput, reproducibility, and organizational learning.
Here's how you will contribute:
- Independently define, plan, and execute complex protein production, purification, and characterization strategies across multiple discovery and platform initiatives. Establish technical milestones, decision criteria, dependencies, and risk-mitigation plans.
- Lead the design, optimization, scale-up, and troubleshooting of protein expression workflows, including transient mammalian and cell-free protein synthesis platforms. Provide technical input into construct design, molecular biology, and stable-expression activities as needed.
- Lead purification workflow development from capture through polishing, with particular emphasis on larger-scale or later-stage protein production. Design and interpret chromatography screening studies, including predictor-plate approaches, resin selection, operating-condition optimization, and scale translation.
- Produce high-quality protein material across a range of formats and scales. Partner with downstream stakeholders to establish fit-for-purpose quality attributes and acceptance criteria based on intended use.
- Select, apply, and interpret appropriate analytical and biochemical characterization methods to assess protein purity, identity, concentration, oligomeric state, aggregation, stability, and other relevant quality attributes.
- Integrate expression, purification, and characterization data to identify root causes, resolve complex technical challenges, evaluate trade-offs, and recommend next steps. Clearly communicate the evidence, assumptions, risks, and uncertainty supporting technical decisions.
- Serve as a technical point of contact for protein production, purification, and characterization strategy. Influence cross-functional decisions by translating scientific findings into clear recommendations for discovery, platform, analytical, and data-focused partners.
- Lead technical interactions with CROs, CDMOs, vendors, and other external partners as appropriate, including defining technical work packages, supporting method or process transfer, reviewing data, troubleshooting issues, and ensuring that deliverables meet scientific requirements.
- Drive the development of scalable, reproducible, and well-documented workflows. Advance the thoughtful use of automation, high-throughput approaches, structured experimental data, and AI/ML-enabled tools to improve scientific productivity and learning.
- Develop and share new methods, technical standards, and best practices. Advise and mentor colleagues, provide constructive scientific feedback, and contribute to an inclusive, collaborative, and high-performing team.
- Demonstrate accountability for scientific quality and delivery by tracking progress, proactively surfacing risks, and communicating successes, setbacks, and lessons learned with clarity and transparency.
The Ideal Candidate will have:
- Independently define, plan, and execute complex protein production, purification, and characterization strategies across multiple discovery and platform initiatives. Establish technical milestones, decision criteria, dependencies, and risk-mitigation plans.
- Lead the design, optimization, scale-up, and troubleshooting of protein expression workflows, including transient mammalian and cell-free protein synthesis platforms. Provide technical input into construct design, molecular biology, and stable-expression activities as needed.
- Lead purification workflow development from capture through polishing, with particular emphasis on larger-scale or later-stage protein production. Design and interpret chromatography screening studies, including predictor-plate approaches, resin selection, operating-condition optimization, and scale translation.
- Produce high-quality protein material across a range of formats and scales. Partner with downstream stakeholders to establish fit-for-purpose quality attributes and acceptance criteria based on intended use.
- Select, apply, and interpret appropriate analytical and biochemical characterization methods to assess protein purity, identity, concentration, oligomeric state, aggregation, stability, and other relevant quality attributes.
- Integrate expression, purification, and characterization data to identify root causes, resolve complex technical challenges, evaluate trade-offs, and recommend next steps. Clearly communicate the evidence, assumptions, risks, and uncertainty supporting technical decisions.
- Serve as a technical point of contact for protein production, purification, and characterization strategy. Influence cross-functional decisions by translating scientific findings into clear recommendations for discovery, platform, analytical, and data-focused partners.
- Lead technical interactions with CROs, CDMOs, vendors, and other external partners as appropriate, including defining technical work packages, supporting method or process transfer, reviewing data, troubleshooting issues, and ensuring that deliverables meet scientific requirements.
- Drive the development of scalable, reproducible, and well-documented workflows. Advance the thoughtful use of automation, high-throughput approaches, structured experimental data, and AI/ML-enabled tools to improve scientific productivity and learning.
- Develop and share new methods, technical standards, and best practices. Advise and mentor colleagues, provide constructive scientific feedback, and contribute to an inclusive, collaborative, and high-performing team.
- Demonstrate accountability for scientific quality and delivery by tracking progress, proactively surfacing risks, and communicating successes, setbacks, and lessons learned with clarity and transparency.
Education and Experience
- Ph.D. in biochemistry, molecular biology, bioengineering, chemical engineering, protein sciences, or a related discipline, with typically 4 or more years of relevant industry experience; or B.S. or M.S. in a relevant scientific or engineering discipline, with typically 12 or more years of relevant industry experience; or an equivalent combination of education and experience that demonstrates the technical depth, independent judgment, and scope of impact required for the role.
Nice to Have
- Experience with stable-expression systems and stable cell-line development activities.
- Experience with construct design, cloning, vector design, or related molecular-biology workflows.
- Experience working with engineered proteins, multispecifics, novel scaffolds, or other complex protein modalities.
- Experience integrating protein design information into expression, purification, or characterization strategies.
- Experience with automation, high-throughput experimentation, laboratory information systems, or structured experimental-data environments.
- Experience managing technical work conducted by CRO, CDMO, or vendor partners.
- Experience developing workflows or methods that were adopted beyond an immediate project or work group.
Who Will Love This Job:
This is an opportunity to shape how Generate produces, characterizes, and learns from protein material in a modern, data-rich discovery environment. Your work will directly influence critical scientific decisions while improving the speed, quality, scale, and reproducibility of workflows used across discovery and platform initiatives.
You will combine hands-on science with meaningful technical ownership, broad cross-functional collaboration, and the opportunity to develop approaches that enable the advancement of next-generation biologics.
About Generate Biomedicines
We are a clinical-stage generative biology company pioneering the AI revolution in drug design and development. We are advancing a new approach to drug creation—one grounded in the ability to design proteins with defined biological intent. By integrating machine learning with large-scale experimentation, this approach aims to reduce the uncertainty, time, and cost associated with developing protein-based medicines.
Founded in 2018, we are advancing a growing pipeline of clinical and preclinical programs across multiple disease areas and protein modalities. By unifying computational design and clinical development within a single operating model, we translate this approach into clinical-stage programs and are leading a shift from traditional drug discovery toward systematic drug generation.
At Generate:Biomedicines, we collaborate across disciplines in new ways to invent and innovate. We bring diverse perspectives to a shared goal of delivering better medicines to patients in need, faster, guided by our values and leadership behaviors.
Generate:Biomedicines is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.
Recruitment & Staffing Agencies: Generate:Biomedicines does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Generate:Biomedicines or its employees is strictly prohibited unless contacted directly by the Company's internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Generate:Biomedicines and the Company will not owe any referral or other fees with respect thereto.
See all 4,191+ H-1B Visa Scientist Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new H-1B Visa Scientist Jobs.
Get Access To All JobsTips for Finding H-1B Visa Sponsorship as a Scientist
Match your degree to the SOC code
USCIS evaluates whether your degree field directly relates to your scientist role using the SOC code on the LCA. Pull the O*NET profile for your specialty, biological scientist, chemist, materials scientist, to confirm the listed education requirements match your credentials before applying.
Target employers with certified LCA history
Not every lab or research organization files H-1B petitions regularly. Use the OFLC Wage Search to verify whether a prospective employer has certified LCAs for scientist roles in your specialty, this signals real sponsorship capacity, not just stated willingness.
Verify your role clears the specialty occupation threshold
Scientist positions at federal contractors or national labs sometimes have job descriptions broad enough to trigger an RFE from USCIS. Your offer letter and job duties should explicitly require a specific degree field, not just a generic science background, to satisfy the specialty occupation standard.
Use Migrate Mate to filter by H-1B filing history
Search Migrate Mate to surface scientist roles at employers with verified DOL Labor Condition Application filing records. Targeting employers who have sponsored before reduces uncertainty and speeds up your path from offer to petition filing.
Ask about prevailing wage level during offer negotiation
DOL requires employers to pay at least the prevailing wage for your SOC code and work location. Use the OFLC Wage Search to look up Level I through Level IV wages for your scientist specialty before negotiating, so you can confirm the offered salary satisfies the LCA requirement.
File during cap season with your 60-day grace period in mind
If you're transitioning from OPT or CPT, your employer must file your H-1B petition during the April cap season for an October 1 start. Factor in the 60-day grace period after OPT expiration when timing your job search and offer acceptance.
H-1B Visa Scientist: Frequently Asked Questions
Do scientist roles qualify as a specialty occupation for H-1B purposes?
Most scientist positions qualify when the role requires a bachelor's degree or higher in a specific scientific discipline, chemistry, biology, environmental science, or a related field. The key is that the degree field must be directly tied to the job duties. Roles with vague requirements like 'any science degree' can face scrutiny from USCIS, so the job description should specify the discipline.
Which types of employers sponsor H-1B visas for scientists?
Pharmaceutical companies, biotech firms, national laboratories, government contractors, academic research institutions, and environmental consulting firms are among the most active H-1B sponsors for scientist roles. To find employers with verified filing history rather than guessing, browse scientist listings on Migrate Mate, which surfaces roles at employers with documented LCA certifications through DOL.
How does the prevailing wage requirement affect scientist H-1B petitions?
Before filing an H-1B petition, your employer must obtain a certified LCA from DOL confirming the offered salary meets the prevailing wage for your SOC code in the work location. Prevailing wages vary by specialty and geography, a materials scientist in San Francisco faces a different wage floor than the same role in Ohio. Use the OFLC Wage Search to look up the applicable wage level before accepting an offer.
Can a scientist on OPT transfer to H-1B status without leaving the U.S.?
Yes. If your employer files an H-1B cap-subject petition during the April filing window and it's selected in the lottery, USCIS can approve a change of status from F-1 OPT to H-1B effective October 1, without you leaving the country. If your OPT expires before October 1, the cap-gap rule extends your authorization as long as the petition is timely filed and pending.
What documentation strengthens an H-1B petition for a scientist role?
Strong petitions include a detailed job description that lists specific scientific duties tied to your degree field, transcripts showing your major and coursework, and an expert opinion letter if your degree title doesn't exactly match the job title. If you hold a three-year international degree, an academic credential evaluation establishing equivalency to a U.S. bachelor's degree is also important for satisfying USCIS standards.