Senior Scientist, Synthetic Enabling Technologies

Sanofi; Cambridge (MA); On-site; USD 146,000; Full time

Job summary

A leading global healthcare company is seeking a Senior Scientist in Synthetic Enabling Technologies. This role involves designing synthetic pathways, conducting laboratory scouting, and collaborating within project teams to advance drug development. Ideal candidates will hold a Ph.D. and possess significant experience in synthetic organic chemistry.

Benefits

Health and wellness benefits

Parental leave

Qualifications

• Ph.D. required in related field.
• Strong publication record in peer-reviewed journals.
• Experience with chemocatalysis or biocatalysis.

Responsibilities

• Design novel synthetic pathways for drug substances.
• Conduct route scouting to demonstrate synthetic viability.
• Collaborate with project teams to develop drug substance manufacturing processes.

Skills

Analytical skills

Collaboration

Synthetic organic chemistry

Communication

Education

Ph.D. in organic or synthetic chemistry

Tools

Microsoft suite

Data analysis software

Scifinder-n

Reaxys

Job description

Senior Scientist, Synthetic Enabling Technologies

Senior Scientist, Synthetic Enabling Technologies

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This range is provided by Sanofi. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$145,166.66/yr - $145,166.66/yr

Job Title: Senior Scientist, Synthetic Enabling Technologies

Location: Cambridge, MA

About The Job

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.

The Process Chemistry team, part of the CMC Synthetics organization within Sanofi R&D, is responsible for the design and preliminary process development of commercial manufacturing routes for drug substances undergoing clinical development. We strongly believe that innovation is an important driver to be successful and we focus a large part of our activity on developing new synthetic routes, concepts, and technologies to provide drug substances in the most efficient, robust, economical, environmentally benign, and intrinsically safe way.

We are looking for a highly motivated and collaborative individual with expertise in synthetic organic chemistry to join our Process Chemistry team. Under the direction of Process Chemistry leadership, the primary responsibility of this role is to perform and oversee multi-step route evaluation and route development activities, with the aim of establishing commercial drug substance manufacturing processes through management and execution of internal and outsourced laboratory activities. Depending on projects, this role may also oversee the activities of one or more collaborators.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main Responsibilities

• Design novel synthetic pathway for drug substances in clinical development.
• Conduct route scouting in laboratory to demonstrate synthetic viability.
• Use all imaginable chemistry tools and methods to develop new synthetic pathways (photochemistry, biochemistry, flow chemistry, electrochemistry, on-line analysis, High Throughput Screening, structural analysis (NMR, UPLC/MS).
• Analyze experimental data to drive synthetic experimental plans.
• Assist in the design, planning and execution of multi-step experimental studies guided by risk assessment to deliver safe, efficient, robust and scalable drug substance manufacturing processes.
• Investigate optimization and scale-up of reaction and purification unit operations.
• Collaborate within project teams by working closely with analytical chemists, process engineers, pilot plant experts and project managers within the CMC Synthetics organization.
• Communicate scientific results in a clear, concise, and accurate manner via electronic laboratory notebook documentation, development reports, project discussions and presentations.
• Draft and review technical reports, external publications and patent applications.
• May include management of outsourced laboratory activities: generating scope of work, supervising activities at CDMOs, validating reports for outsourced activities.
  
  

About You

Qualifications & Experience:

• Ph.D. in organic or synthetic chemistry.
• Knowledge in at least one of the following areas: advanced analytics, flow chemistry, high throughput experimentation.
• Experience in chemocatalysis or biocatalysis including characterization of catalytic processes and/or mechanistic analysis.
• Computational capabilities and basic coding skills.
• Strong publication record in peer-reviewed journals.
• Excellent written and verbal communication skills.
• Ability to operate with flexibility in a dynamic environment and with tight deadlines.
• Post-doctoral experience.
• Proficiency with Microsoft suite.
• Familiarity with digital tools (e.g. Scifinder-n, and Reaxys) and advanced data analysis software (e.g. Spotfire).
• Design of experiment, statistical and/or thermo-kinetic modeling.
• Strategic and innovative thinker with a track record of fresh insightful thinking by developing creative approaches to processes and practices.
• French language skills
  
  

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 Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse 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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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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Pharmaceutical Manufacturing

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