Urwah Admin

Sanofi

<div>Title: Research Associate III
Pay range: $54.00 - $71.00 per hour (paid weekly)
Work Schedule: 1st shift 9am-5pm EST
Location: Framingham, MA - On Site<h3 class="jobSectionHeader">
Contract Length: 12 months with 12 month extension</h3> 
Description:
Sanofi&rsquo;s contingent workforce program, FLEXT Direct, is seeking a highly motivated candidate for a Research Associate III position within the Cell Line Development (CLD) team. This role involves creating recombinant CHO cell lines to support research and preclinical development programs within Sanofi.
The successful candidate will work in a high-performing, fast-paced, and collaborative environment, contributing to the end-to-end development of recombinant CHO cell lines and the optimization of platforms for future CHO expression systems. This work will directly support the advancement of projects in Sanofi&rsquo;s biologics pipeline.<h3 class="jobSectionHeader"> 
Position Overview / Key Responsibilities:</h3><ul><li>
Assist in generation of engineered mammalian cell lines (transfection pools, clones) expressing candidate biotherapeutics</li><li>
Assist in several studies simultaneously to optimize cell line generation processes</li><li>
Perform mammalian cell culture techniques:</li><li>
Sterile technique</li><li>
Cell counting</li><li>
Passaging</li><li>
Cryopreservation</li><li>
Perform basic molecular biology techniques:</li><li>
DNA plasmid preparation</li><li>
PCR</li><li>
Restriction enzyme digestion</li><li>
Demonstrate self-motivation with excellent attention to detail and superb organizational skills</li><li>
Work collaboratively and communicate transversally across teams</li><li>
Maintain flexibility in a fast-paced, goal-oriented environment, with a willingness to expand and broaden skillset</li><li>
Prepare reports, presentations, and data sets to effectively communicate results, progress, and plans</li><li>
Apply strong technical background to support experimental goals</li><li>
Manage and present data effectively</li><li>
Contribute to lab organization, reagent tracking, and other laboratory support tasks</li><li>
Ensure compliance with all applicable regulations; perform work safely and maintain accurate records in accordance with SOPs and company policies</li><li>
Present data at regular lab meetings</li></ul><h3 class="jobSectionHeader"> 
Basic Qualifications:</h3><ul><li>
Bachelor&rsquo;s Degree or Master&rsquo;s Degree in Biology, Cellular Biology, Molecular Biology, or an equivalent field (preferably with a focus in Cellular Biology research)</li></ul><h3 class="jobSectionHeader"> 
Preferred Qualifications:</h3><ul><li>
Experience in suspension culture of CHO cell lines in a pharmaceutical or biotechnology setting</li><li>
Knowledge of techniques such as cell culture and molecular manipulations</li></ul></div>

USA - Research Associate III (Scientific) (contract)

<div>Job title: Supply Chain Manager - External Manufacturing APAC GenMed<ul><li>
Grade: L3-1</li><li>
Location &ndash; Mumbai</li></ul> 
About the job 
We are seeking an experienced Supply Chain Manager to oversee External Manufacturing (EM) India plant supply chain operations for our portfolio across contract manufacturing sites. Join a global network that powers how Sanofi delivers &mdash; seamlessly, purposefully, and at scale. In Manufacturing &amp; Supply, you&rsquo;ll help reimagine how life-changing treatments reach people everywhere, faster. 
About Sanofi:
We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; 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&rsquo;s lives. 
Key Responsibilities:
Operations Management<ul><li>
Lead the team and support Material Planning Systems (MPS, MRP) and align with Contract Manufacturing Organizations (CMOs) and vendors to ensure timely deliveries</li><li>
Lead monthly S&amp;OP meetings with markets and suppliers to capture demand, identify supply risks, and implement mitigation strategies</li><li>
Collaborate with Procurement and supplier for material and logistics support to ensure on-time deliveries with optimal cost control</li><li>
Implement inventory control measures and maintain Inventory Service Levels (ISL) as per global policies and internal SLAs</li><li>
To review production schedule and manage demand for all products of domestic, export flow &amp; regional CMO sites</li><li> Monitor CMO KPI compliance with respect to On Time In Full (OTIF), Delivery performance, Out of stock (OOS), Min-Max stocks coverage</li></ul><ul><li> 
Ensuring on the Price revisions (MRP) and artwork changes implementation in time across all CMO&rsquo;s</li><li>
undefined</li><li>
Ensure on timely Release of purchase order to CMO&rsquo;s and RM/PM suppliers and availability of finished goods to central hub from CMO sites</li><li>
undefined</li></ul>
Digital Planning &amp; Analytics<ul><li>
Experience with advanced planning systems (APS) and supply chain optimization tools.</li><li>
Proficiency in data visualization and analytics tools like Power BI</li></ul><ul><li>
Hands-on experience with Enterprise Resource Planning (ERP) systems SAP S/4 HANA</li><li>
Responsible for digital transformation projects within supply chain operations</li></ul> 
Process Standardization &amp; Budget Control<ul><li>
Ensure all tasks comply with Segregation of Duties and maintain uniform processes across multi-country operations with validated SOPs</li><li>
Collect forecasts, develop assumptions for budget processes, and monitor budget adherence</li></ul>
Master Data Management<ul><li>
Oversee and manage master data management activities for EM India operations including material master and flow management</li></ul>
Performance Analysis &amp; Reporting<ul><li>
Support data collection on orders and deliveries across CMOs and prepare monthly report</li><li>
Analyze performance through power BI dashboards to enable faster decision-making</li><li>
Prepare ad-hoc reports and data analysis as requested by management</li></ul> 
About you
Experience- 8-12 years of industrial experience in supply chain management
Qualifications -Bachelor&rsquo;s or Master&rsquo;s degree in Business Administration, Pharmaceutical, Engineering, Operations, or other similar relevant disciplines
Technical Skills<ul><li>
Hands on Experience in SAP ERP. SAP S/4 HANA knowledge is added advantage</li><li>
Experience in advanced planning systems (APS). Knowledge of Rapid response Kinaxis or Maestro is preferred</li><li>
Proficient in supply chain management, inventory management, and material planning</li></ul> 
Pursue Progress. Discover Extraordinary.
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what&rsquo;s never-been-done-before. You&rsquo;ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people&rsquo;s lives? Let&rsquo;s Pursue Progress and Discover Extraordinary &ndash; together. 
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
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Senior Manager- Supply Chain

<div>
 <ul>
 <li>
 About the job
 
 
 </li>
 </ul>
 Supply Chain Function ensures product availability and distribution efficiency, through managing end-to-end supply chain operations, coordinating with local warehousing and logistics partners, implementing global supply chain strategies to ensure supporting business continuity and supply chain resilience.
 
 
 
 About Sanofi
 
 
 
 We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; 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&rsquo;s lives.
 
 
 
 Main Responsibilities
 
 
 
 <ul>
 <li>
 Coordinate and prepare for EDA inspection visits, including dossier compilation, logistics, and documentation.
 </li>
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 Submit and follow up on NORCB pre-evaluation files until final reports are issued.
 </li>
 <li>
 Oversee sample submission and analysis at NORCB, ensuring timely release of conformity reports.
 </li>
 <li>
 Track and manage all supporting documents (e.g., CPPs, GMPs) required for product release.
 </li>
 <li>
 Maintain accurate records and archives of all submissions, reports, and communications.
 </li>
 <li>
 Ensure compliance with all applicable regulatory guidelines and internal procedures.
 </li>
 <li>
 Manage procurement and timely delivery of reagents, reference standards, and other analytical materials for batch release.
 </li>
 <li>
 Support regulatory activities by coordinating sample withdrawals for new registrations, renewals, and variations.
 </li>
 <li>
 Act as the focal point for post-marketing surveillance of imported products with the EDA.
 </li>
 <li>
 Oversee the importation process in alignment with EDA regulations.
 </li>
 <li>
 Ensure adherence to HSE and compliance standards..
 
 
 </li>
 </ul>
 
 About You
 
 
 
 <ul>
 <li>
 Education: Bachelor&rsquo;s degree in Pharmaceutical Sciences or a related medical field.
 </li>
 <li>
 Experience: Minimum 4 years in regulatory affairs, quality assurance, or a related field within the pharmaceutical industry.
 </li>
 <li>
 Skills: Strong command of English (written and spoken)
 </li>
 <li>
 Proficient in Microsoft Office
 </li>
 <li>
 Excellent communication and negotiation skills
 </li>
 <li>
 Strong organizational and planning abilities
 </li>
 <li>
 Ability to manage multiple priorities under pressure
 </li>
 <li>
 Effective cross-functional collaboration and problem-solving skills
 </li>
 <li>
 Ability to meet deadlines
 </li>
 <li>
 Teamwork
 </li>
 <li>
 LEAD competencies: Act for Change, strive for results, Cooperate Transversally, Commit to Customer
 
 
 </li>
 </ul>
 
 Why choose us?
 
 
 
 Ready to push the limits of what&rsquo;s possible? Join Sanofi in one of our corporate functions and you can play a vital part in the performance of our entire business while helping to make an impact on millions around the world.
 
 
 <ul>
 <li>
 Make your work count by supporting a company that brings life-changing treatments to millions &mdash; and is committed to doing right by patients, communities, and the planet.
 </li>
 <li>
 Drive progress from within by helping simplify, scale, and modernize how a global biopharma business delivers smarter, faster, and more sustainably.
 </li>
 <li>
 Support teams across science, medicine, and operations by building better systems, shaping bold strategies, and enabling innovation at speed.
 </li>
 <li>
 Make an impact across borders and functions, collaborating with leaders to turn complex challenges into real-world solutions.
 </li>
 <li>
 Advance your career through stretch roles, cross-functional moves, and development opportunities designed to match your ambition.
 </li>
 <li>
 Thrive in inclusive, high-performing teams where every role matters and every voice helps shape what&rsquo;s next.
 
 
 </li>
 </ul>
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 Pursue
 
 
 Progress
 
 .
 
 Discover
 
 
 Extraordinary
 
 .
 
 
 Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what&rsquo;s never-been-done-before. You&rsquo;ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people&rsquo;s lives? Let&rsquo;s Pursue Progress and Discover Extraordinary &ndash; together.
 
 
 At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
</div>

Logistics Coordinator (1 year contract)

<div>Job title: Summer-Fall 2026 Co-Op - Purification Process Development
Location: Framingham, 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 Purification Process Development group develops manufacturing processes for purification of therapeutic proteins (e.g., antibodies, enzymes, and multi-specifics) from cell culture harvest and provides technical support to GMP downstream process operations.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people&rsquo;s lives. We&rsquo;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:<ul><li>
Conducting experiments using small-scale chromatography columns and filtration units and/or high-throughput technologies to develop, characterize, and optimize new processes</li><li>
The student may also contribute to technology development projects focused on next-generation bioprocessing and process development technologies, such as integrated and continuous bioprocessing, high-throughput process development, and mechanistic modeling of bioprocesses</li><li>
On-the-job training will be provided as necessary to teach the technical skills required to perform their duties</li></ul>
About You
Basic Qualifications:<ul><li>
Currently enrolled and pursuing a bachelor's, master's, or Ph.D. degree in biology, chemistry, chemical or biochemical engineering, biotech, or a related field at an accredited college or university with the expectation that you will complete your current degree by the Spring of 2028
</li><li>Must be able to relocate to the office location and work 40hrs/week, Monday-Friday, for the full duration of the co-op/internship</li><li>
Must be permanently authorized to work in the U.S. and not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually require future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship</li></ul>
Preferred Qualifications:<ul><li>
Ability to organize and communicate ideas and results in a clear and concise manner</li><li>
Ability to interact with multiple co-workers and function effectively in a team environment</li></ul>
Why Choose Us?<ul><li>
Bring the miracles of science to life alongside a supportive, future-focused team.</li><li>
Discover endless opportunities to grow your talent and drive your career, whether it&rsquo;s through a promotion or lateral move, at home or internationally.</li><li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.</li><li>
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&rsquo; gender-neutral parental leave.</li><li>
Exposure to cutting-edge technologies and research methodologies.</li><li>
Networking opportunities within Sanofi and the broader biotech community.</li></ul> 
The salary range for this position is $29-$57 hourly. 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 LINK.
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.
#GD-SA
 
#LI-SA
#LI-Onsite
#vhd
null</div>

Summer-Fall 2026 Co-Op - Purification Process Development

<div>Job Title: Summer-Fall 2026 Co-Op - Process Modelling
Location: Framingham, 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 proposed position is based within the Process Modeling and Data Science group within CMC Development, R&amp;D. Our group is comprised of process modelers and data scientists focused on using mechanistic, data-driven, and hybrid models to accelerate process development activities. 
This project aims to develop high fidelity models to support development of protein capture and polishing steps. In addition to model development and calibration, this project will explore the use of alternative error metrics and advanced tools to improve model evaluation and robustness. The candidate may also leverage optimization and uncertainty quantification tools to enhance model calibration, sensitivity analysis. These efforts are expected to increase model fidelity and build confidence for broader application in process development.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people&rsquo;s lives. We&rsquo;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:<ul><li>
The ideal co-op candidate will have knowledge and hands-on experience in modeling of chromatography using mechanistic (e.g., transport-dispersive, general rate, or lumped rate) or hybrid approaches. An understanding of experimental requirements will be important to effectively collaborate with downstream scientists and iteratively improve the overall modeling workflow.</li><li>
This is an exciting opportunity to demonstrate the benefits of process modeling and data science towards accelerating the development of cutting-edge medicines that will improve the quality of life for patients across the world.</li></ul>
About You
Basic qualifications:<ul><li>
Currently pursuing a master's degree or PhD in Chemical, Biochemical Engineering or related field at an accredited college or university
</li><li>Must be able to relocate to the office location and work 40hrs/week, Monday-Friday, for the full duration of the co-op
</li><li>Must be authorized to work in the US for the duration of the co-op</li><li>
Experience with programming skills in languages such as Python, MATLAB, or R</li><li>
Experience in developing mechanistic or hybrid models for chromatography using either custom code or existing tools (such as GoSilico, Cadet etc.)</li></ul>
Preferred Qualifications:<ul><li>
Understanding of experimental chromatography workflows</li><li>
Interest or experience in evaluating model performance using a variety of error metrics</li><li>
Exposure to tools for optimization, sensitivity analysis, or uncertainty quantification</li><li>
Experience with statistics and AI/ML</li><li>
Ability to work in a cross-functional team with modelers and downstream scientists</li></ul><div><div>
Why Choose Us?</div><div><ul><li>
Bring the miracles of science to life alongside a supportive, future-focused team.</li><li>
Discover endless opportunities to grow your talent and drive your career, whether it&rsquo;s through a promotion or lateral move, at home or internationally.</li><li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.</li><li>
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&rsquo; gender-neutral parental leave.</li><li>
Exposure to cutting-edge technologies and research methodologies.</li><li>
Networking opportunities within Sanofi and the broader biotech community.</li></ul></div></div><div><div> 
The salary range for this position is $45-$60 hourly. 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 LINK.
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.</div></div>
#GD-SA
 
#LI-SA
#LI-Onsite
#vhd
null</div>

Summer-Fall 2026 Co-Op - Process Modelling

<div>Job Title: Senior Scientist<div><div><div><div><div><div><div><div><div>
Location: Cambridge, MA</div></div></div></div></div></div></div></div></div>
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.
We are seeking a highly motivated and innovative Senior Scientist with experience in rare muscle and/or neuromuscular disorders with expertise in mechanisms impacting disease progression, including inflammation, fibrosis, atrophy and regeneration. The successful candidate will bring a broad range of in vitro, in vivo and/or in silico skills to support current pipeline programs and lead the exploration of novel pathways and targets for initiation of new programs. We are a team that encourages creativity and proactiveness to unlock new therapeutic avenues. This is an exciting opportunity to make an early and meaningful impact on therapies for patients with devastating neuromuscular diseases.
The successful candidate will play a key role in identifying novel therapeutic opportunities and expanding our pipeline into new indications. They will contribute across research, clinical, and business development efforts, helping to align scientific insights with strategic goals. This position offers a unique opportunity to shape the future of therapeutics for rare muscle and/or neuromuscular disorders and help deliver transformative treatments to patients worldwide.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people&rsquo;s lives. We&rsquo;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:<ul><li>
Apply scientific expertise and judgement to design, execute, analyze and document in vitro and in vivo studies to support pipeline and exploratory programs.</li><li>
Explore disease biology to identify and validate new targets and pathways for preclinical programs.</li><li>
Design and conduct mechanism-of-action and proof-of-concept studies to evaluate therapeutic strategies.</li><li>
Implement cutting-edge methodologies and leverage internal technology platforms to strengthen data packages.</li><li>
Lead and coordinate outsourced research activities with CROs.</li><li>
Initiate and support on-going collaborations with academic partners.</li><li>
Maintain high-quality data documentation.</li><li>
Prepare and present data in internal meetings and at external conferences.</li><li>
Contribute to the preparation of publications, patents, and technical reports.</li></ul>
About You
Qualifications
Basic Requirements<ul><li>
Ph.D. in a scientific field with relevant experience in industry or academia; or a master&rsquo;s degree with 4+ years of relevant experience; or bachelor&rsquo;s degree with 6+ years relevant experience.</li><li>
A degree in Molecular Biology, Cellular Biology, or a related discipline is preferred.</li><li>
Strong knowledge of skeletal muscle and/or neuromuscular biology.</li><li>
Experience studying mechanisms of muscle pathology in neuromuscular diseases (e.g., inflammation, fibrosis, atrophy, regeneration).</li><li>
Hands-on expertise in molecular, cellular, and biochemical methods, assay development, and in vitro and in vivo disease models.</li><li>
Experience preparing high-quality documents including experimental protocols, SOPs, technical reports, and presentations.</li><li>
Track record of significant contributions to research projects and scientific publications.</li></ul>
Preferred Experience<ul><li>
Experience with cell-based models for muscle biology (primary/immortalized myoblasts, satellite cells).</li><li>
Expertise with animal models of muscle disease (dystrophic models, muscle injury model).</li><li>
Experience performing muscle functional measurements in rodents.</li><li>
Hands-on experience performing single nuclei isolation from skeletal muscle for single-nuc RNASeq.</li><li>
Computational biology experience in RNA-Seq and/or single nucleus/cell RNA-Seq data analysis.</li></ul>
Core Competencies<ul><li>
Ability to work independently as well as part of cross-functional teams in a highly collaborative and matrixed environment.</li><li>
Ability to multi-task and adapt to rapidly changing priorities and deadlines.</li><li>
Excellent critical thinking, analytical, and problem-solving skills.</li><li>
Excellent written and oral communication skills, with the ability to communicate effectively in a multidisciplinary team.</li><li>
Strong interpersonal skills, with the ability to build excellent working relationships.</li><li>
Exceptional organizational and time-management skills, lab notebook practices, and attention to detail.</li></ul>
Why Choose Us?<ul><li>
Bring the miracles of science to life alongside a supportive, future-focused team.</li><li>
Discover endless opportunities to grow your talent and drive your career, whether it&rsquo;s through a promotion or lateral move, at home or internationally.</li><li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.</li><li>
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&rsquo; gender-neutral parental leave.</li></ul>
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.
#GD-SA 
#LI-SA 
#LI-Onsite
#vhd
#mRNA
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.</div>

Senior Scientist

<div>Job Title: Senior Scientist - RNA-Molecular Biology and Rare Neurological Diseases<div><div><div><div><div><div><div><div><div>
Location: Cambridge, MA</div></div></div></div></div></div></div></div></div>
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.
We are seeking a highly motivated and skilled Senior Scientist with deep expertise in RNA biology and and rare diseases&mdash;particularly affecting the central nervous system, including rare neurodegenerative conditions such as Huntington&rsquo;s disease, and leukodystrophies. The ideal candidate will bring robust hands-on experience in RNA regulation, RNA-binding proteins, and computational biology, combined with a strong foundation in disease biology.
In this role, you will lead efforts to discover and validate novel RNA-based therapeutic targets and strategies, leveraging both wet-lab and computational approaches. Your work will play a critical role in advancing our rare disease pipeline, particularly in rare CNS-related indications. You will collaborate closely with cross-functional teams to translate scientific insights into new programs, contributing to the strategic expansion of our therapeutic portfolio.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people&rsquo;s lives. We&rsquo;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:<ul><li>
Drive new program initiation by applying expertise in disease mechanisms and RNA biology</li><li>
Design, develop, and implement computational tools for the analysis of high-throughput sequencing datasets, with a focus on RNA-level insights</li><li>
Leverage molecular biology skills in combination with disease area expertise to translate computational findings into actionable biological hypotheses and experimental designs in the context of rare neurological/neurodevelopmental disorders</li><li>
Design and conduct in vitro and in vivo mechanism-of-action, and proof-of-concept studies to validate targets and evaluate therapeutic strategies</li><li>
Contribute to interdisciplinary research programs in a highly collaborative manner across internal groups and with external partners, with opportunity to grow into a project leadership role</li><li>
Prepare high-quality analyses, interpretation, documentation, and presentations to support project milestones, publications, patent filings, and potentially regulatory (IND/CTA) filings</li><li>
Present findings and progress in internal meetings and external venues as appropriate (e.g., publications, conferences, collaboration and governance meetings)</li></ul> 
About You
Basic Qualifications:<ul><li>
Ph.D. in a scientific field with relevant experience in industry or academia; or a master&rsquo;s degree with 4+ years of relevant experience; or bachelor&rsquo;s degree with 6+ years relevant experience.</li><li>
Degrees in Molecular Biology, Cellular Biology, or a related discipline is preferred</li><li>
Deep expertise in RNA and molecular biology, including RNA regulation and processing (e.g., splicing, stability, transport), and the roles of regulatory RNAs and RNA-binding proteins</li><li>
Proficiency in computational and bioinformatics techniques, including RNA-seq analysis, isoform and splice-site mapping, and off-target prediction</li><li>
Demonstrated ability to produce high-quality scientific documentation, including experimental protocols, standard operating procedures (SOPs), technical reports, and presentations</li><li>
Proven track record of meaningful contributions to research programs, evidenced by scientific publications and/or presentations</li></ul>
Preferred Qualifications:<ul><li>
Hands-on experience with disease-relevant in vitro and/or in vivo models, including functional and phenotypic assays</li><li>
Technical proficiency in iPSC culture, gene expression analysis, molecular cloning, vector design, gene editing (e.g., CRISPR), and RNA sequencing (bulk and single-cell)</li><li>
Experience with discovery, optimization, and development of siRNAs and/or ASOs (degrading and skipping) is a plus</li><li>
Experience performing in vivo studies in rodent models</li><li>
Familiarity with drug discovery and development processes</li></ul> 
Skills and competencies:<ul><li>
Ability to work independently and collaboratively within cross-functional, matrixed teams</li><li>
Highly adaptable, with strong multitasking skills and the ability to manage shifting priorities and timelines</li><li>
Strong analytical and problem-solving skills with sound scientific judgment</li><li>
Clear written and verbal communication skills, with the ability to convey complex concepts clearly</li><li>
Interpersonal strengths that foster effective collaboration and the ability to build productive working relationships</li><li>
Outstanding organizational skills, attention to detail, and commitment to maintaining rigorous documentation</li></ul>
Why Choose Us?<ul><li>
Bring the miracles of science to life alongside a supportive, future-focused team.</li><li>
Discover endless opportunities to grow your talent and drive your career, whether it&rsquo;s through a promotion or lateral move, at home or internationally.</li><li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.</li><li>
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&rsquo; gender-neutral parental leave.</li></ul>
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.
#GD-SA 
#LI-SA 
#LI-Onsite
#vhd
#mRNA
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.</div>

Senior Scientist - RNA-Molecular Biology and Rare Neurological Diseases

Join Sanofi and explore 33   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.