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Sanofi

CMC Project Leader

Framingham, MA · On-site

Job Title: CMC Project Leader Location: Framingham, MA About the Job As the CMC Project Lead within our Cluster Mammalian Project team, you'll be accountable for the CMC project activities of ...

Sanofi

CMC Project Leader

Framingham, MA · On-site +1

Job Title: CMC Project Leader Location: Framingham, MA About the Job As the CMC Project Lead within our Cluster Mammalian Project team, you'll be accountable for the CMC project activities of ...

Sanofi

CMC Project Leader

Framingham, MA · On-site +1

Job Title: CMC Project Leader Location: Framingham, MA About the Job As the CMC Project Lead within our Cluster Mammalian Project team, you'll be accountable for the CMC project activities of ...

Sanofi

CMC Project Leader

Framingham, MA · On-site

Job Title: CMC Project Leader Location: Framingham, MA About the Job As the CMC Project Lead within our Cluster Mammalian Project team, you'll be accountable for the CMC project activities of ...

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How much do cmc project jobs pay per hour?

As of May 30, 2026, the average hourly pay for cmc project in the United States is $21.55, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.28 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a CMC Project Manager, and why are they important?

To thrive as a CMC (Chemistry, Manufacturing, and Controls) Project Manager, you need expertise in pharmaceutical development, regulatory requirements, and project management, often supported by a degree in life sciences or engineering. Familiarity with tools such as project management software (e.g., MS Project), quality management systems, and regulatory submission platforms is essential. Strong organizational skills, effective communication, and cross-functional leadership are critical soft skills for coordinating complex projects and teams. These abilities ensure that CMC projects meet regulatory standards, timelines, and quality objectives, leading to successful drug development and approval.

What are some common challenges faced by CMC Project Managers when coordinating cross-functional teams in pharmaceutical development?

CMC Project Managers often work with diverse teams, including scientists, regulatory specialists, and manufacturing experts, which can present challenges in aligning timelines, priorities, and communication styles. Navigating regulatory requirements while ensuring technical milestones are met requires strong organizational skills and proactive problem-solving. Effective CMC Project Managers facilitate clear communication, manage dependencies between functions, and adapt plans as project needs evolve, all while keeping the project on track for successful submissions.

What are CMC Project managers?

CMC Project managers oversee the Chemistry, Manufacturing, and Controls (CMC) aspects of drug development and production. They coordinate activities across various teams, ensuring that pharmaceutical products meet regulatory standards for quality, safety, and efficacy. Their responsibilities include managing timelines, budgets, documentation, and communication between research, manufacturing, and regulatory affairs. CMC Project managers play a critical role in bringing new drugs to market efficiently and compliantly.

What is the difference between Cmc Project vs Cmc Specialist?

AspectCmc ProjectCmc Specialist
CredentialsTypically requires a degree in life sciences or related field, with experience in project managementRequires a degree in chemistry, pharmacy, or related field, with knowledge of CMC regulations
Work EnvironmentInvolves managing cross-functional teams in pharmaceutical or biotech companiesFocuses on technical CMC activities, often within R&D or manufacturing settings
Industry UsageUsed in project planning, coordination, and oversight of CMC activitiesUsed in executing specific CMC tasks, data review, and regulatory submissions

The main difference is that a Cmc Project manages overall CMC activities and timelines, while a Cmc Specialist focuses on technical execution and data handling within those projects.

More about Cmc Project jobs
What are the most commonly searched types of Cmc Project jobs? The most popular types of Cmc Project jobs are:
What job categories do people searching Cmc Project jobs look for? The top searched job categories for Cmc Project jobs are:
Cmc Project jobs near you
Infographic showing various Cmc Project job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $44,814 per year, or $21.5 per hour.
CMC Project Leader

CMC Project Leader

Sanofi

Framingham, MA • On-site

Full-time

Posted 9 days ago

Sanofi rating

8.2

Company rating: 8.2 out of 10

Based on 58 frontline employees who took The Breakroom Quiz

27th of 70 rated pharmaceutical

Job description

Job Title: CMC Project Leader
Location: Framingham, MA
About the Job
As the CMC Project Lead within our Cluster Mammalian Project team, you'll be accountable for the CMC project activities of mammalian projects of Sanofi's R&D pipeline from early to late clinical phases up to submission and approval. Ready to get started?
Join the engine of Sanofi's mission - where deep immunoscience meets bold, AI-powered research. In R&D, you'll drive breakthroughs that could turn the impossible into possible for millions.
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.
Main Responsibilities:
The CMC Project Leader is accountable for the CMC project activities of mammalian projects of Sanofi's R&D pipeline from early to late clinical phases up to submission and approval which includes:
  • Lead a cross-functional CMC team with functional members/sub-team leaders from CMC R&D and IA, including Mammalian DS platform, Drug product and formulation platform, Bioanalytics, Device development, Quality, Regulatory CMC, CMC Dossiers, Project Management and Demand & Supply
  • Oversight in CMC and sub teams of approximately 100 to 200 employees
  • Create a strategic and integrated CMC development plan based on global project objectives
  • Represent the CMC team and function as core member in the Global Project Team, contributing to overall project strategy and execution of the appropriate actions within CMC to achieve project goals.
  • Define the Quality Target Product Profile (QTPP).
  • Act as overall product/process expert for the project and provide technical and scientific expertise on major project topics; drive technical and scientific discussion and alignment within the CMC team and in R&D/M&S cross-functional governance meetings
  • Accountable for quality of CMC contributions to clinical and PPQ work packages (DS/DP/Analytics), and CMC elements for regulatory submissions and consultations.
  • Drive technical excellence, initiates and oversees CoGs evaluations and align project strategy with commercial expectations.
  • Drive within the CMC team the evaluation of CMC risks and appropriately escalate to Senior Management and provide mitigation plans.
  • Alert decision makers and stakeholders to risks that can impact critical program timelines.
  • Responsible for implementation of CMC deliverables within budget considering external and internal costs.
  • Lead the planning of CMC project budget including communication and alignment with global project team and senior management.

About You
Basic Qualifications:
  • Bachelor's or master's degree in biotechnology, pharmaceutical engineering, pharmaceutical analysis, biochemistry, chemical engineering or related discipline with a minimum of 16 years of relevant industry experience or PhD with minimum of 12 years of relevant industry experience.
  • Experience in biologics development.
  • CMC regulatory experience in IND filing.
  • Experience in leading international, cross-functional project teams.
  • Expertise in project management and risk assessment.
  • Demonstrated leadership experience
  • Excellent communication skills; fluency in English

Preferred Qualifications:
  • Expertise in Biologics CMC area, with proven experience in at least two scientific areas, e.g., analytics, process dev., regulatory CMC, manufacturing, etc.
  • Comprehensive scientific background in biotechnology and/or protein science.
  • Experience working in a matrix organization.
  • Experience and understanding of current Pharmaceutical environment including the economic and regulatory challenges. Experience in BLA submission.
  • Strong leadership capabilities, strong team spirit and capacity to coordinate several activities and stakeholders, excellent communication skills, stakeholder management and networking.

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.

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.
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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.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
US and Puerto Rico Residents Only
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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:
$206,250.00 - $297,916.66
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.

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About Sanofi

Sourced by ZipRecruiter

At Sanofi R&D North America, we deliver meaningful solutions for patients. We transform science into breakthrough, best-in-class and first-in-class medicines and vaccines. We believe in creating a diverse and inclusive workforce - and workplace - which brings together the collective brainpower of over 2,000 colleagues and provides you with an exciting place to grow and develop. We set the bar high, and we deliver.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Bridgewater, NJ, US

Year founded

2004

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