Analytical Scientist Visa Sponsorship Jobs in Massachusetts
Analytical scientist visa sponsorship jobs in Massachusetts are concentrated in the state's dense life sciences corridor, spanning Cambridge, Boston, and Waltham. Major employers include Pfizer, Novartis, Takeda, and Thermo Fisher Scientific. Roles typically sit within pharmaceutical development, biotech QA, and materials research, requiring advanced chemistry, biology, or related STEM degrees.
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Get Access To All JobsJob title: mRNA Analytical Development Senior Scientist
Location: Waltham, MA
About the job
In order to strengthen the Biochemical and Biophysical group in R&D Analytical Sciences Department, Sanofi Pasteur is looking for a skilled and highly motivated individual to develop novel methods and improve characterization of mRNA vaccines in development by working closely with the bioprocess development group.
Analytical Sciences Department has the overall responsibility to develop, qualify and validate robust analytical methods to support release and characterization testing of mRNA Drug Substances and Drug Products candidates in development.
Join the team protecting half a billion lives every year with next-gen science, mRNA innovation, and AI-driven breakthroughs. In Vaccines, you’ll help advance prevention on a global scale - and shape the future of immunization.
About Sanofi:
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world and are supported and enhanced through our diverse portfolio of medical device and diagnostic products. Together, we chase the miracles of science to improve people’s lives.
Main Responsibilities:
- Develop advanced technology for biochemical, biophysical, and bioassay assay development in support of mRNA vaccine process and product development, product release, stability, and comparability study.
- Work with analytical leads supporting CMC activities.
- Write and review method documentation and characterization reports in support of regulatory filings.
- Ensure timely completion of assignments and deliverables. Independently design and execute complex experiments. Author method development and investigation reports.
- Manage assay testing at CROs if required, support investigation, deviation, and change control.
- Participate internal non-GMP and GMP lab set up and product release and stability testing.
- Supervise and train junior scientists.
- Compliant to Sanofi Quality standards and HSE policy. Participate in continuous improvement of laboratory safety and quality compliance.
About you
Basic Qualifications
- PhD or Master's Degree in Biochemistry, Biology, Cell Biology, Analytical Chemistry, Biotechnology or related sciences.
- Ph.D. with a minimum of 3 years of experience in the pharmaceutical or biotechnology industry, or a Master's degree with a minimum of 6 years of experience in the pharmaceutical or biotechnology industry.
- Previous CMC analytical development experience.
- Expertise in LC (RP, IEX, SEC, HILIC) and one or more of the following techniques but not limited to CGE, spectroscopy, particle analysis.
- Ability to perform complex method development and propose appropriate method improvement suitable for CMC space.
Preferred
- Knowledge of nucleic acid/oligonucleotides chemistry and standard analytical methods of these molecules.
- LC-MS experience.
- Hands on experience in quality control laboratory environment is a plus.
Why choose us?
- Bring the miracles of science to life alongside a supportive, future-focused team.
- Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
- Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
- Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
- Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.
- Help improve the lives of millions of people globally by making drug development quicker and more effective.
- Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.
Sanofi US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
GD-SP
LI-SP
LI-Hybrid
vhd
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
Job title: mRNA Analytical Development Senior Scientist
Location: Waltham, MA
About the job
In order to strengthen the Biochemical and Biophysical group in R&D Analytical Sciences Department, Sanofi Pasteur is looking for a skilled and highly motivated individual to develop novel methods and improve characterization of mRNA vaccines in development by working closely with the bioprocess development group.
Analytical Sciences Department has the overall responsibility to develop, qualify and validate robust analytical methods to support release and characterization testing of mRNA Drug Substances and Drug Products candidates in development.
Join the team protecting half a billion lives every year with next-gen science, mRNA innovation, and AI-driven breakthroughs. In Vaccines, you’ll help advance prevention on a global scale - and shape the future of immunization.
About Sanofi:
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world and are supported and enhanced through our diverse portfolio of medical device and diagnostic products. Together, we chase the miracles of science to improve people’s lives.
Main Responsibilities:
- Develop advanced technology for biochemical, biophysical, and bioassay assay development in support of mRNA vaccine process and product development, product release, stability, and comparability study.
- Work with analytical leads supporting CMC activities.
- Write and review method documentation and characterization reports in support of regulatory filings.
- Ensure timely completion of assignments and deliverables. Independently design and execute complex experiments. Author method development and investigation reports.
- Manage assay testing at CROs if required, support investigation, deviation, and change control.
- Participate internal non-GMP and GMP lab set up and product release and stability testing.
- Supervise and train junior scientists.
- Compliant to Sanofi Quality standards and HSE policy. Participate in continuous improvement of laboratory safety and quality compliance.
About you
Basic Qualifications
- PhD or Master's Degree in Biochemistry, Biology, Cell Biology, Analytical Chemistry, Biotechnology or related sciences.
- Ph.D. with a minimum of 3 years of experience in the pharmaceutical or biotechnology industry, or a Master's degree with a minimum of 6 years of experience in the pharmaceutical or biotechnology industry.
- Previous CMC analytical development experience.
- Expertise in LC (RP, IEX, SEC, HILIC) and one or more of the following techniques but not limited to CGE, spectroscopy, particle analysis.
- Ability to perform complex method development and propose appropriate method improvement suitable for CMC space.
Preferred
- Knowledge of nucleic acid/oligonucleotides chemistry and standard analytical methods of these molecules.
- LC-MS experience.
- Hands on experience in quality control laboratory environment is a plus.
Why choose us?
- Bring the miracles of science to life alongside a supportive, future-focused team.
- Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
- Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
- Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
- Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.
- Help improve the lives of millions of people globally by making drug development quicker and more effective.
- Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.
Sanofi US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
GD-SP
LI-SP
LI-Hybrid
vhd
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
Analytical Scientist Job Roles in Massachusetts
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Search Analytical Scientist Jobs in MassachusettsAnalytical Scientist Jobs in Massachusetts: Frequently Asked Questions
Which companies in Massachusetts sponsor visas for analytical scientists?
Massachusetts-based pharmaceutical and biotech employers with active visa sponsorship histories for analytical scientists include Pfizer, Novartis, Takeda Pharmaceuticals, Biogen, Sanofi Genzyme, and Thermo Fisher Scientific. Contract research organizations such as Charles River Laboratories and Covance also file regularly for these roles. Sponsorship activity is concentrated in Cambridge, Waltham, and the greater Boston metropolitan area.
Which visa types realistically fit analytical scientist roles in Massachusetts?
Analytical scientist positions typically qualify as specialty occupations requiring a bachelor's degree or higher in chemistry, biochemistry, or a related field. H-1B visa is the most common pathway, though it is subject to an annual cap and selection process. H-1B1 visa applies to Chilean and Singaporean nationals. Qualified candidates may also pursue EB-2 or EB-3 employment-based green cards through PERM labor certification. F-1 OPT and STEM OPT are available to recent graduates holding STEM-designated degrees.
How to find analytical scientist visa sponsorship jobs in Massachusetts?
Migrate Mate lists Massachusetts employers with verified visa sponsorship history for analytical scientist roles, searchable by location and role type. Because sponsorship intent is not always stated in job postings, searching a platform built around employer LCA filing history saves significant time. Focus searches on Cambridge, Boston, and Waltham, where the highest concentration of life sciences employers actively hiring for these positions is found.
Which cities in Massachusetts have the most analytical scientist sponsorship jobs?
Cambridge leads the state due to its dense cluster of biotechnology and pharmaceutical firms anchored around Kendall Square. Boston's Longwood Medical Area adds hospital and research institute hiring. Waltham and Lexington host numerous established pharma and specialty chemical employers. Worcester has a growing biotech presence tied to its university medical ecosystem, making it a secondary market worth monitoring for analytical scientist openings.
Are there state-specific factors that affect analytical scientist visa sponsorship in Massachusetts?
Massachusetts has one of the highest concentrations of life sciences employers in the United States, which translates to consistent demand for analytical scientists and relatively broad sponsorship activity compared to most other states. The state's university pipeline, including MIT, Harvard, and Northeastern, feeds research-intensive employers who are experienced with H-1B and STEM OPT hiring. Candidates with backgrounds in pharmaceutical analysis, mass spectrometry, or chromatography are particularly well positioned in this market.
What is the prevailing wage for sponsored analytical scientist jobs in Massachusetts?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.