Associate Scientist Green Card Jobs
Associate Scientist roles in biotech, pharma, and research institutions qualify for EB-2 and EB-3 green card sponsorship through the PERM labor certification process. Employers file a permanent petition on your behalf, leading to lawful residency rather than a temporary visa. Specialized lab and research skills make this pathway highly viable for foreign professionals.
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INTRODUCTION
We are seeking a dynamic senior associate scientist to join bioanalytical & biomarker technologies group. The candidate will design and execute analytical and bioanalytical method to support biotherapeutics discovery and preclinical development. The individual should be experienced in executing HPLC and/or LC-MS based methods from sample preparation, instrument operation to data analysis. The successful candidate will be expected to work cross-functionally in a collaborative, fast-paced, multidisciplinary team environment and have the opportunity to explore new technologies while growing technical depth.
ROLE AND RESPONSIBILITIES
A Typical day in this role looks like:
- Design, execute, and troubleshoot LC‑MS and HPLC methods for analytical characterization of bioconjugates and bioanalytical quantification of therapeutics.
- Support a range of modalities—including monoclonal antibodies (mAbs), antibody–drug conjugates (ADCs), siRNA/oligonucleotides, and endogenous biomarkers—across diverse biological matrices.
- Perform end‑to‑end sample preparation (e.g., LLE, SPE, affinity capture, enzymatic digestion, homogenization) and operate LC‑MS/MS workflows from instrument setup to data analysis.
- Analyze and interpret results; summarize findings, propose next steps, and present data at internal meetings.
- Document experiments, methods, and results in electronic lab notebooks (ELNs) with clarity and rigor; contribute to SOPs and method documentation.
- Maintain instruments and general lab readiness; troubleshoot systems and ensure data integrity and instrument uptime.
- Evaluate and implement new platforms, workflows, and automation to improve throughput, sensitivity, and robustness.
- Prioritize effectively across multiple projects and timelines, collaborating closely with colleagues in discovery biology, DMPK/PK‑PD, and process/analytical teams.
BASIC QUALIFICATIONS
This role may be for you, if you have experience:
- BS or MS degree in Chemistry, Biochemistry, Pharmaceutical Science or a related discipline with 3+ years hand-on experience.
- Experience in liquid chromatography and/or mass spectrometry is preferred, with the ability to execute, qualify and optimize analytical methods.
- Hands on experience in sample preparation techniques (LLE, SPE, affinity capture, enzymatic digestion, homogenization, etc.); experience with automation platforms is a plus.
- Detail-oriented, good interpersonal and effective technical communication skills (written and verbal).
- Ability to manage multiple projects in a fast-paced environment.
- Collaborative team player with a growth mindset to quickly adapt to evolving priorities and continuously learn to embrace new challenges.
- Previous exposure in bioanalysis of LC-MS based small molecule, oligonucleotides, biomarkers and biotherapeutics assay development is beneficial.
COMPENSATION
- Salary Range (annually): $80,300.00 - $131,100.00
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.
Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

INTRODUCTION
We are seeking a dynamic senior associate scientist to join bioanalytical & biomarker technologies group. The candidate will design and execute analytical and bioanalytical method to support biotherapeutics discovery and preclinical development. The individual should be experienced in executing HPLC and/or LC-MS based methods from sample preparation, instrument operation to data analysis. The successful candidate will be expected to work cross-functionally in a collaborative, fast-paced, multidisciplinary team environment and have the opportunity to explore new technologies while growing technical depth.
ROLE AND RESPONSIBILITIES
A Typical day in this role looks like:
- Design, execute, and troubleshoot LC‑MS and HPLC methods for analytical characterization of bioconjugates and bioanalytical quantification of therapeutics.
- Support a range of modalities—including monoclonal antibodies (mAbs), antibody–drug conjugates (ADCs), siRNA/oligonucleotides, and endogenous biomarkers—across diverse biological matrices.
- Perform end‑to‑end sample preparation (e.g., LLE, SPE, affinity capture, enzymatic digestion, homogenization) and operate LC‑MS/MS workflows from instrument setup to data analysis.
- Analyze and interpret results; summarize findings, propose next steps, and present data at internal meetings.
- Document experiments, methods, and results in electronic lab notebooks (ELNs) with clarity and rigor; contribute to SOPs and method documentation.
- Maintain instruments and general lab readiness; troubleshoot systems and ensure data integrity and instrument uptime.
- Evaluate and implement new platforms, workflows, and automation to improve throughput, sensitivity, and robustness.
- Prioritize effectively across multiple projects and timelines, collaborating closely with colleagues in discovery biology, DMPK/PK‑PD, and process/analytical teams.
BASIC QUALIFICATIONS
This role may be for you, if you have experience:
- BS or MS degree in Chemistry, Biochemistry, Pharmaceutical Science or a related discipline with 3+ years hand-on experience.
- Experience in liquid chromatography and/or mass spectrometry is preferred, with the ability to execute, qualify and optimize analytical methods.
- Hands on experience in sample preparation techniques (LLE, SPE, affinity capture, enzymatic digestion, homogenization, etc.); experience with automation platforms is a plus.
- Detail-oriented, good interpersonal and effective technical communication skills (written and verbal).
- Ability to manage multiple projects in a fast-paced environment.
- Collaborative team player with a growth mindset to quickly adapt to evolving priorities and continuously learn to embrace new challenges.
- Previous exposure in bioanalysis of LC-MS based small molecule, oligonucleotides, biomarkers and biotherapeutics assay development is beneficial.
COMPENSATION
- Salary Range (annually): $80,300.00 - $131,100.00
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.
Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
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Get Access To All JobsTips for Finding Green Card Sponsorship as an Associate Scientist
Align your degree to PERM requirements
PERM filings require your foreign degree to match the job's minimum requirements exactly. Get a credential evaluation confirming your bachelor's or master's aligns with the U.S. SOC classification for Associate Scientist roles before applying.
Target employers with active PERM filings
Biotech and pharmaceutical companies that have already run PERM for similar roles understand the process and are far less likely to withdraw sponsorship mid-cycle. Search DOL disclosure data to confirm prior Associate Scientist filings before accepting an offer.
Search green card sponsoring employers on Migrate Mate
Filter Associate Scientist openings by employers with verified green card sponsorship history on Migrate Mate. This surfaces companies already familiar with PERM, I-140, and adjustment of status, which cuts negotiation time significantly.
Confirm the recruitment process meets DOL standards
PERM requires your employer to advertise the role, document that no qualified U.S. worker applied, and certify prevailing wages via the OFLC Wage Search. Ask your employer or HR team how they handle this documentation to avoid audit delays.
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Find Associate Scientist JobsAssociate Scientist Green Card Sponsorship: Frequently Asked Questions
Does an Associate Scientist role qualify for EB-2 or EB-3 sponsorship?
It depends on how the employer defines the position's minimum requirements. Roles requiring a master's degree or a bachelor's plus five years of specialized research experience typically qualify for EB-2. Roles requiring only a bachelor's degree fall under EB-3. The PERM application locks in the category based on the job description, not your personal credentials, so the offer letter wording matters significantly.
How does green card sponsorship differ from H-1B sponsorship for this role?
H-1B sponsorship is temporary, requires renewal every three years, and subjects you to the annual lottery unless you're cap-exempt. EB-2 and EB-3 green card sponsorship through PERM leads to permanent residency with no cap lottery. The tradeoff is timeline: PERM and I-140 together can take one to two years before you reach the adjustment of status stage, and applicants from certain countries face additional priority date backlogs.
How do I find Associate Scientist employers willing to sponsor a green card?
Migrate Mate lets you filter Associate Scientist roles by employers with verified employment-based green card sponsorship history. This is more reliable than asking during interviews, since it surfaces companies that have already completed PERM filings for similar roles and understand the full I-140 and adjustment of status process.
What does the PERM process look like for a research or lab role?
Your employer files a PERM application with DOL certifying the role, the prevailing wage from the OFLC Wage Search, and proof that no qualified U.S. worker was displaced. DOL either certifies or audits the application. Certification typically takes six to eighteen months, after which your employer files the I-140 petition with USCIS. Lab and research roles with tightly defined technical skill requirements tend to have lower audit risk than broadly defined positions.
Can I change employers after my I-140 is approved?
Yes, under AC21 portability rules, if your I-485 has been pending for at least 180 days and you move to a similar role in the same or related occupation, your priority date and approved I-140 remain valid. Associate Scientist roles in adjacent research fields generally qualify as similar enough, but USCIS reviews the SOC codes and job duties, so confirm the match with your new employer before resigning.
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