New · posted Nov 14
Sanofi · Pharmaceuticals
QC Analyst
- Framingham, MA
- On-site
- Full-time
- Associate & Specialist
The role
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.
What you need
3 ways to qualify
High school
+ 4+ years of experience
High School Diploma/GED with a minimum of 4 Years of any industry experience.
- or
Associate
+ 2–4 years of experience
Associate Degree with 2-4 Years of any industry experience.
- or
Bachelor’s
+ 0–2 years of experience
Bachelor’s Degree with 0-2 Years of any industry experience.
Basic Qualifications
- Proficient with Microsoft Office tools such as Word, Excel & PowerPoint
Additional Accountabilities
- Ability to perform tasks in a Quality Control Laboratory environment and capable of lifting at least 10 pounds. May be required to pass vision exam to perform specific responsibilities. May be required to enter into controlled environments following proper gowning protocols.
Preferred Qualificationsnice to have
- 1 Year of Experience in a GMP lab environment.
- Experience with lab-based data management systems.
- Experience in a Quality Control Laboratory.
What you'll do
- Collect Environmental Monitoring (Viable Air, Viable Surface, Non-Viable Air Samples) and Critical Utility (RO, DI, WFI, Steam Water Samples, and Compressed Air and Mixed Gases Samples) in a timely manner, ensuring adherence to the committed scheduled plans
- Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks
- Recording all expected raw data, calculations, information related to his/her tasks, to comply with cGMP and data integrity requirements
- Ensuring that he/she is trained and qualified to the assigned analytical testing that requires to be qualified
- Performing the QC data review of executed tests by other analysts in a timely manner, ensuring adherence to the committed scheduled plans
- Informing his/her manager of any quality or HSE event (deviations, OOS,) in a timely manner to ensure investigation and impact assessment are performed appropriately
- Participating actively to any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriately
- Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately
Pay and benefits
$49,920 – $66,560 a year
Employer provided$24.00 – $32.00 an hour · yearly at 2,080 hours (40 a week)
How this comparesNorth America Applicants Only
The salary range for this position is:
$24.00 - $32.00
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.
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.
14weeks
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.
Where you'll work
Framingham, MAOn-siteOpen in Maps (opens in a new tab)
More jobs in Framingham, MAWorking conditions
- Work in a laboratory with minimal use of chemicals
- Ability to lift at least 10lbs
From the posting
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 people’s lives.
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.
Equal opportunity, accessibility and legal noticesSanofi's statements, word for word
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.
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
Job intelligence
The context around this role
Live data · November 14, 2026
Salary intelligence
How the pay compares
This role's midpoint is 20% below the US median for Quality Control roles at this level.
This roleEmployer provided
Associate & Specialist roles in Massachusetts13 roles publishing pay
Associate & Specialist roles in the US81 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $49,920 | — | $66,560 |
| Massachusetts (middle half) | $72,000 | $85,000 | $96,000 |
| All US (middle half) | $62,500 | $73,000 | $88,500 |
This role: Sanofi's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, November 14, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 254 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Sanofi's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 17 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods6
- GMP and compliance3
- Data and digital systems3
- Documentation and SOPs2
- Investigations and CAPA2
- Clinical trial conduct1
- Collaboration and leadership1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Control work in pharmaceuticals, led by the three this posting names, each linked to the agency or standards body that publishes it.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticalsNamed in the posting
- FDAFDA OOS guidance(official source, opens in a new tab)Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical ProductionNamed in the posting
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and AnswersNamed in the posting
- USPUSP–NF(official source, opens in a new tab)US Pharmacopeia general chapters and monographs, such as <61> bioburden, <85> endotoxin, <1225> validation
- FDAFDA aseptic processing guidance(official source, opens in a new tab)Sterile Drug Products Produced by Aseptic Processing: Current Good Manufacturing Practice
- ISOISO 14644-1(official source, opens in a new tab)Cleanroom air cleanliness classification by particle concentration
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- ICHICH Q2(R2) and Q14(official source, opens in a new tab)Validation and development of analytical procedures
- FDAFDA analytical procedures guidance(official source, opens in a new tab)Analytical Procedures and Methods Validation for Drugs and Biologics
- ICHICH Q1 stability testing(official source, opens in a new tab)Stability testing of drug substances and drug products
- EDQMEuropean Pharmacopoeia(official source, opens in a new tab)The Ph. Eur. quality standards for medicines in Europe, published by the EDQM
- ICHICH Q3 impurities(official source, opens in a new tab)Impurities in drug substances and products, residual solvents and elemental impurities
- EUEU GMP (EudraLex Volume 4)(official source, opens in a new tab)The EU's good manufacturing practice rules, including Annex 1 sterile and Annex 15 validation
- ISOISO/IEC 17025(official source, opens in a new tab)Competence of testing and calibration laboratories
- ICHICH Q7(official source, opens in a new tab)Good manufacturing practice for active pharmaceutical ingredients
- ISPEISPE GAMP 5(official source, opens in a new tab)A risk-based approach to compliant GxP computerized systems
Company hiring pulse
Sanofi on Regulatory Jobs
- 26
- Open roles
- 26
- Distinct roles
- 7
- Locations
By discipline
- Quality18 69%
- Regulatory4 15%
- Clinical4 15%
By level
- Senior & Principal9 35%
- Associate & Specialist7 27%
- Director5 19%
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QC Analyst at Sanofi
Applications close December 11. $50K–$67K a year, employer provided.