Genzyme Corporation Posted September 9, 2026

Scientist 1 MSAT

Framingham, United States Full time
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Genzyme Corporation is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Title: Scientist 1 MSAT

Location: Framingham, MA

About the Job

The Scientist I will develop and execute bioassays across various biologic modalities in support of commercial manufacturing and continuous improvement initiatives. In addition, this role will support Stability study management and the execution of biochemical and biophysical assays, as needed.

Join a global network that powers how Sanofi delivers, seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.

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. Together, we chase the miracles of science to improve lives.

Main Responsibilities

Execute cell-based assays and immunoassays to assess product potency, biological activity, and impurities (e.g., residual DNA, HCPs) in support of late-stage programs, commercial biologics, and life cycle management programs

Develop and optimize analytical methods including cell-based assays, ELISA, and flow cytometry for MSAT projects and technology transfer activities; perform general biochemical and biophysical assays under SME supervision, as needed

Perform method qualification and transfer in and out of the department

Work with analytical leads and relevant stakeholders to support sample stability studies

Ensure timely completion of assignments and deliverables; independently design and execute complex experiments under general supervision

Participate in characterization and comparability studies

Author protocols, method development/technical reports, data analysis summaries, and investigation reports

Write and review method documentation and characterization reports in support of regulatory filings

Collaborate with other scientists in the team, as well as interact cross-functionally in the Global MSAT organization and interface functions and organizations, such as CMC, Quality, Manufacturing, CMO/CROs as appropriate

About You

Basic qualifications:

PhD with 0–1+ years' experience in the biopharmaceutical industry, OR Master's degree with 3+ years' experience, OR Bachelor's degree with 6+ years' experience in the pharma/biotech industry within analytical development

Scientific background in cell biology, biochemistry, molecular biology, immunology, or a related field

3+ years hands-on experience with cell-based assays, immunoassays (e.g., ELISA), and/or flow cytometry in a laboratory setting

Experience in experimental design, method development, and qualification

Strong analytical and problem-solving skills with the ability to troubleshoot complex assay issues and interpret scientific data

Knowledge of mammalian cell culture and commercial protein purification processes

Experience with bioanalytical equipment, software, and statistical tools for high-level data analysis

Proficiency in data analysis tools and laboratory information management systems.

Skills and Competencies:

Highly organized and detail-oriented with a demonstrated commitment to quality and accuracy

Able to work independently and collaboratively within cross-functional teams and with external partners; enthusiastic, self-motivated, and agile in responding to urgent requests, with the initiative to lead new tasks

Excellent written and oral communication skills with the ability to present complex technical information clearly

Strong time management and ability to prioritize multiple projects

Ability to work full-time onsite in an analytical lab environment

Preferred qualifications:

Experience with method development, method qualification, and/or validation

Knowledge and hands-on experience with sample stability testing and management

Hands-on experience and comprehensive knowledge of other biochemical and biophysical techniques, including but not limited to U/HPLC, CGE, cIEF, spectroscopy, and particle analysis

Familiarity with biologics manufacturing (monoclonal antibodies, vaccines, or other biotherapeutics)

Experience working on highly technical projects requiring adaptability and responsiveness.

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.

Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.

Power industry-leading performance by leveraging digital, data, and AI-driven innovation – at speed and scale

Transform lives worldwide by delivering life-changing treatments anywhere, anytime.

Sanofi Inc. 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-SG

#LI-GZ

#VHD

#LI-Onsite

Pursue progress , discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

Sanofi US endeavours to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-866-SANOFI2 (1-866-726-6342) or click here

US and Puerto Rico Residents Only

Sanofi Inc. 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.

North America Applicants Only

The salary range for this position is:

$85,500.00 - $123,500.00

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 details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Framingham, United States
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 3428 comparable Manufacturing & CMC roles across 175 biopharma companies.

3428Comparable roles tracked
3174Currently active
175Companies hiring similar roles
61Countries represented

Salary context

812 of 3428 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject $85,500/yr – $123,500/yr
Lowest disclosed · Operator – Plant Utilities · Lilly $13/hr – $28/hr (≈ $26,998–$58,302/yr)
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $42,650 – $381,150 (median $127,500)

Where these roles are based

Top locations among the 3428 comparable roles

United States1570
Germany211
India155
France149
Ireland129
China125

+ 55 more countries

Seniority mix

1516 of 3428 peers have a known seniority level

Senior408
Manager359
Intern/Fellow/Postdoc208
Associate149
Principal129
Associate Director105
Director104
Senior Director48
Executive/VP6

Therapeutic area mix

22 of 3428 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease13
Rare Disease3
Dermatology & Aesthetics2
Oncology2
Immunology1
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
40%similar
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40%similar
Lilly Indianapolis, Indiana, United States of America Associate
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40%similar
Merck West Point, Pennsylvania, United States of America Principal
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40%similar
Merck West Point, Pennsylvania, United States Intern/Fellow/Postdoc
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40%similar
AbbVie North Chicago, IL Associate Director
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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
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Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
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AbbVie · North Chicago, IL · Senior
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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.