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Sanofi

Sanofi is an R&D driven, AI-powered biopharma company dedicated to improving people's lives through innovative medicines and vaccines. With a deep understanding of the immune system, Sanofi develops treatments that address urgent healthcare challenges globally. The company is committed to delivering growth while making a positive impact on communities and the environment.

<div><h1 class="jobSectionHeader">About the job</h1>
Within Sanofi`s Global Device and Packaging Unit, the Senior Packaging Engineer is in charge to ensure robust and reliable device manufacturing development strategies and thus implementation.
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>
Drive end-to-end planning and execution of process and manufacturing concept development for DDC &amp; OSD packaging solutions</li><li>
Serve as global interface and strategic facilitator between multiple Sanofi sites and Packaging Development, ensuring standardization and harmonization of equipment and processes across the network</li><li>
Implement LEAN and Design for Manufacturing (DfM) principles throughout development and industrialization phases of DDC &amp; OSD products, aligned with strategic business planning</li><li>
Develop innovative, robust packaging manufacturing technologies that meet commercial requirements and regulatory standards</li><li>
Define and standardize technical requirements for manufacturing processes and equipment specifications across all platforms</li></ul>
Tasks, jurisdiction and responsibilities<ul><li>
Develop and implement packaging concepts and processes for DDC &amp; OSD manufacturing, establishing robust and scalable production systems</li><li>
Drive innovative packaging manufacturing technologies, integrating commercial requirements, device specifications, and GMP compliance</li><li>
Lead standardization of technical requirements (e.g., pFMEA) across all device &amp; packaging platforms, Sanofi sites, and CMOs</li><li>
Apply LEAN and DfM principles to ensure robust industrialization of development products aligned with business planning</li><li>
Manage RFQ preparation, quote review, economic efficiency calculations, and support investment decision-making</li><li>
Lead feasibility studies and implement strategic goals in packaging concepts, aligning new investments with business objectives</li><li>
Identify and drive optimization projects in close collaboration with production sites, R&amp;D, Quality, and Commercial teams, managing implementation and conceptualization</li><li>
Provide lifecycle support and lead RCA/CAPA activities across the device &amp; packaging network, resolving complex technical problems and driving continuous improvement</li></ul><h1 class="jobSectionHeader">
About you</h1>
Experience :
<ul><li>Several years of professional experience in the pharmaceutical industry</li><li>
Knowledge of FDA and other regulatory requirements such as cGMP and MDD / ISO 13485</li><li>
Experience in the implementation of qualification and/or validation projects (CSV)</li><li>
Experience in the area of inspections by authorities</li></ul>
Soft skills:<ul><li>
Simplifying complexity &amp; proactive risk anticipation</li><li>
Willingness for transversal cooperation across functional boundaries / departments</li><li>
Active driving of changes / optimizations in the area of delegation</li><li>
Result and solution orientation, willingness to assume responsibility</li><li>
Team orientation / team player with excellent communication skills</li><li>
Self-reliant and systematic way of working</li><li>
High willingness to communicate and ability to work in a team</li></ul>
Technical skills:<ul><li>
Very good process and packaging knowledge of the CMO and Sanofi Device Business.</li><li>
Proven expertise in pharmaceutical manufacturing, GxP documentation and related Equipment Qualification and Process Validation of high throughput equipment.</li></ul>
Education: Bachelor (Master is a plus) in engineering (e.g. packaging, mechanical, automation)
Languages: Fluent in English, French or German basic knowledge is a plus<h1 class="jobSectionHeader">
Why choose us?</h1><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>
We take care of you and your family with a wide range of health and social such as high-quality healthcare, numerous prevention programs and coverage for long-term illness. Our 14-week paid family leave for both parents is outstanding as well as a wide range of childcare benefits.</li><li>
Start your career in Frankfurt, Germany and experience our modern working environment and benefit from hybrid, flexible working time models.</li></ul></div>

Senior Packaging Engineer (all genders)

<div>About the Role
The Translational In Vivo Models (TIM) department within Sanofi's R&amp;D is seeking an exceptional Distinguished Scientist to lead our Transgenic Model &amp; Technology (TMT) function globally. This strategic leadership role will drive innovation in genome engineering and genetically modified model development to accelerate drug discovery across all therapeutic divisions.
Being responsible in this role you will ensure our organization remains at the forefront of technical developments in genome engineering, enabling breakthrough discoveries in immunology, immuno-inflammation, rare diseases, neuroscience, and oncology. You will serve as a key scientific advisor and strategic thinker, shaping the direction of in vivo and preclinical research programs while championing the integration of emerging technologies &mdash; including AI and digital platforms &mdash; into transgenic science.
This role is based in Frankfurt/M. and is primarily office/lab-based.
About Sanofi
We are an innovative global healthcare company, chasing the miracles of science to improve people's lives. Our team, across some 100 countries, is dedicated to transforming the practice of medicine by working to turn the impossible into the possible. We provide potentially life-changing treatment options and life-saving vaccine protection to millions of people globally, while putting sustainability and social responsibility at the center of our ambitions. Sanofi is guided by four core values: Aim Higher, Act for Patients, Be Bold, and Lead Together.
Main Responsibilities
Scientific Leadership &amp; Innovation<ul><li>Lead and advance state-of-the-art genome engineering techniques and mouse genetics applications for in vivo model development supporting discovery and developmental research</li><li>Apply personal expertise in transgenesis and CRISPR technology to devise and execute sophisticated experimental strategies for target validation, proof-of-concept, and efficacy studies</li><li>Identify, evaluate, and implement new technologies and innovations in transgenesis, CRISPR/Cas systems, and emerging genome engineering platforms</li><li>Serve as a strategic thinker and scientific advisor to research projects across therapeutic areas, providing expert guidance on in vivo and preclinical study design</li><li>Champion the integration of AI and digital technologies to enhance model design, data analysis, and predictive capabilities in transgenic research</li><li>Cover a broad scientific scope including immunology and immuno-inflammation, rare diseases, neuroscience, molecular and immune-oncology, and all areas of cell and molecular biology pertaining to immunology and immune-oncology</li></ul>
Strategic Planning &amp; Cross-Functional Leadership<ul><li>Demonstrate strategic thinking and orientation in aligning transgenic capabilities with organizational research priorities and long-term scientific goals</li><li>Lead and coordinate transversal teams and projects across multiple therapeutic divisions, sites, and external partners</li><li>Collaborate closely with the Head of Transgenic Division, drug discovery program leaders, cluster heads, and department heads to provide strategic scientific advice</li><li>Drive budget planning, forecasting, and financial management to optimize resource allocation and operational efficiency</li></ul>
Operational Excellence &amp; Partnership Management<ul><li>Establish and maintain comprehensive project management frameworks ensuring full-service delivery from model design through study-ready animal production</li><li>Build and manage strategic relationships with model providers, CROs, and academic partners for development and delivery of genetically modified models</li><li>Negotiate and oversee license agreements and partnership contracts for model acquisition and technology access</li><li>Implement quality standards and continuous improvement initiatives to maintain operational excellence</li></ul>
People Leadership &amp; Development<ul><li>Supervise, mentor, and develop staff members to build a high-performing team at the forefront of transgenic science</li><li>Participate in talent management decisions including hiring, promotions, performance evaluations, and organizational development</li><li>Foster a culture of scientific excellence, innovation, collaboration, and continuous learning</li></ul>
About you
Education &amp; Experience<ul><li>Ph.D. in Molecular Biology, Genetics, Developmental Biology, or a related discipline</li><li>Extensive post-doctoral or industry experience in mouse molecular genetics and transgenic animal model development</li><li>Demonstrated track record of scientific leadership in an academic or pharmaceutical/biotech research environment</li><li>Minimum of 5 years of demonstrated, hands-on experience performing this role.</li></ul>
Technical Expertise<ul><li>Deep expertise in developing transgenic animal models, including engineering diverse genetic alleles using CRISPR/Cas9, Cas12, base editors, prime editors, and other advanced genome engineering systems</li><li>Comprehensive knowledge of both theoretical principles and practical methodologies required to lead a state-of-the-art transgenic facility</li><li>Strong foundation in molecular biology, mouse genetics, embryology, and reproductive technologies</li><li>Experience across multiple therapeutic areas (immunology, oncology, rare diseases, neuroscience preferred)</li></ul>
Leadership &amp; Strategic Capabilities<ul><li>Proven strategic thinking and orientation with ability to align scientific capabilities with business objectives</li><li>Demonstrated success leading transversal teams and managing complex, multi-stakeholder projects across sites and functions</li><li>Established track record as a scientific thinker and advisor to in vivo and preclinical research programs</li><li>Experience identifying, evaluating, and implementing new technologies and innovations in a research setting</li><li>Familiarity with and application of AI and digital technologies in biological research, model design, and data analysis</li></ul>
Professional Skills<ul><li>Exceptional project management skills with ability to oversee multiple concurrent initiatives</li><li>Strong contract negotiation and vendor management capabilities</li><li>Excellent budget planning, financial management, and resource allocation skills</li><li>Outstanding interpersonal and communication skills (written and verbal) for effective collaboration across diverse, global stakeholders</li><li>Proven ability to work in matrix organizations and influence without direct authority</li></ul>
Personal Attributes<ul><li>Self-motivated with demonstrated ability to lead and thrive in collaborative team environments</li><li>Comfortable managing competing priorities and adapting to dynamic research needs</li><li>Commitment to scientific excellence, integrity, and ethical research practices</li><li>Passion for mentoring and developing scientific talent</li><li>Candidates must be willing to travel as part of this position.</li></ul>
Why choose us?<ul><li>
Opportunity to shape the future of transgenic technology at a global biopharmaceutical leader</li><li>
Access to cutting-edge technologies and resources across a world-class R&amp;D organization</li><li>
Collaborative, innovative research environment spanning multiple therapeutic areas</li><li>
Benefit from a well-thought-out benefits package that rewards your contribution and commitment.</li><li>
We take care of you and your family with a wide range of health and social such as high-quality healthcare, numerous prevention programs and coverage for long-term illness. Our 14-week paid family leave for both parents is outstanding as well as a wide range of childcare benefits.</li><li>
Start your career at an attractive location in the center / in the capital of Germany and experience our modern working environment and benefit from hybrid, flexible working time models.</li></ul>
#LI-Onsite
#TransgenicAnimalModels
#Sanofi
#SanofiCareers
#PursueProgress
#DiscoverExtraordinary
#WeAreSanofi
#IgnitingPotential</div>

Distinguished Scientist – Transgenic Model & Technology (all genders)

<div>Job Title: Clinical Contract Coordinator II 
Location: Cambridge, MA (on-site) 
Contract: 12-months (with possibility of extension) 
Schedule: Monday - Friday; 8 AM - 4 PM ET 
Pay Rate Max: $43 per hour 
Sanofi's contingent workforce program, FLEXT Direct, is seeking a Clinical Contract Coordinator II for a 12-month contract.
The Clinical Contract Coordinator (CCC)&rsquo;s primary mission will involve organizing the biological specimen management laboratory, reception, registration, storage, and shipment of biospecimen for pre-clinical and clinical studies received at a Sanofi Laboratory Site.
The CCC will be secondarily assigned to clinical studies and may be responsible for the collection, processing, storage, and distribution of biological specimens in support of clinical research and development programs. This role ensures compliance with regulatory requirements, quality standards, and ethical guidelines while managing biospecimen operations across multiple studies and sites.
As a CCC you will be directly reporting to the Global head of the Translational medicine operations BSM department or a delegated team lead and will collaborate closely with the global translational medicine operations biospecimen management team in addition to other stakeholders such as local site head of lab sciences, scientists, Precision/Biomarker/PK/ADA leads, clinical operations study/project leads, Data leads, Biomarkers &amp; Bioanalysis outsourcing team.
LOCAL SITE LABORATORY MANAGEMENT RESPONSIBILITIES
You will be responsible for the day-to-day coordination and management of laboratory sample operations, ensuring accurate receipt, processing, storage, and tracking of biological specimen.
You will:<ul><li>
Receive, record, store, dispose, and ship BioSpecimen addressed to the laboratory from across global locations and verify the compliance of the related delivery documentation.</li><li>
Ensure and perform the registration of pre-clinical/clinical study BioSpecimen received in our LIMS (Laboratory Information Management System e.g. Watson) and generate and send documents related to these receptions.</li><li>
Manage the recording of receptions and shipments in dedicated tracking files.</li><li>
You detect, analyze, and report inconsistencies during BioSpecimen reception and registration to the study BioSpecimen Manager who will support you in resolving these inconsistencies.</li><li>
Ensure the creation of study designs in Watson LIMS.</li><li>
Ensure the maintenance of the BSM laboratory work areas and proper functioning of equipment.</li><li>
Ensure work quality in accordance with Good Laboratory and Clinical Practices (GLCP).</li><li>
Monitor regular equipment maintenance and update established documentation.</li><li>
Ensure and perform registration and update of inventories (BioSpecimen, equipment, and consumables).</li><li>
Continuously participate in improving the department's operations and ensure that safety instructions are followed as the Health Safety Environment (HSE) correspondent for BSM.</li><li>
Create and/or update BSM procedures.</li><li>
Participate in meetings and working groups, propose technical, organizational, and documentary improvements (procedures), and participate in process optimizations.</li><li>
Support audits and inspections; act as spokesperson for sample-related processes and documentation.</li></ul>
GLOBAL BIOSPECIMEN MANAGEMENT AND RESPONSIBILITIES
As a CCC you may be assigned perform the BioSpecimen management tasks, monitor clinical studies and oversee end-to-end biospecimen lifecycle from collection through analysis and archival.
You will:<ul><li>
Implement Translational medicine and biospecimen management strategies aligned with clinical development objectives</li><li>
Partner with clinical study teams to integrate biospecimen requirements into study protocols</li><li>
Collaborate with translational medicine and biomarker teams on biospecimen utilization</li><li>
Review study documents such as the protocol, Informed Consent Form, central laboratory specifications, electronic Case Report Form (eCRF) Specifications, Data collection strategy, etc.</li><li>
Lead the design and optimization of biospecimen collection protocols and workflows</li><li>
Create the BioSpecimen Management Plan (SMP) containing instructions for collection, storage, and shipping of BioSpecimen</li><li>
Manage relationships with the Bioanalysis outsourcing, central laboratories, biorepositories, and third-party vendors as needed.</li><li>
Ensure proper chain of custody, tracking, and inventory management of all biospecimens</li><li>
Create reports containing BioSpecimen statuses and perform overall monitoring of these BioSpecimen, from collection to destruction</li><li>
Ensure the traceability of associated documentation in the electronic Trial Master File (eTMF)</li></ul>
EDUCATION
<ul><li>Bachelor&rsquo;s degree required in Biological Sciences, Biomedical Sciences, Biotechnology, Clinical Laboratory Science, Public Health and Life Sciences or related field.</li><li>
3-6 years&rsquo; experience in biospecimen management, clinical laboratory operations managing biospecimens in clinical trials or research settings</li></ul>
SKILLS
<ul><li>Biospecimen Management &amp; Lab Coordination requires end-to-end workflow coordination, timeline planning and milestone tracking, strong biospecimen lifecycle expertise, clinical trial systems &amp; tools experience, LIMS (e.g. Watson) proficiency, and excellent cross-functional coordination skills.</li><li>
Knowledge of regulatory requirements (GCP, GCLP, CLIA, CAP) and quality standards</li><li>
Proficiency with Laboratory Information Management Systems (LIMS) and specimen tracking platforms</li><li>
Experience with clinical trial sample management</li><li>
Knowledge of ICH-GCP guidelines and regulatory requirements</li><li>
Familiarity with Clinical trial management &amp; electronic data capture (EDC) systems</li><li>
May require flexibility to support urgent sample processing needs &amp; Manual dexterity</li><li>
Strong communication, team management capabilities and fluency in English</li><li>
Experience with global, multi-site clinical studies preferred</li><li>
Experience with biospecimen banking or biorepository operations preferred</li><li>
Project management experience preferred</li></ul></div>

USA - Clinical Contract Coordinator II (Clinical) (contract)

<div>
 
 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.
 
 
 
 About The Job
 
 
 
 Our Team:
 
 
 The Africa medical Team at Sanofi is a high-performing team of medical leaders who are a trusted source of scientific and medical information and share insights; effective and innovative strategic partners to our internal and external stakeholders; and dedicated to public health. We represent diverse experiences and backgrounds which strengthen our team and mirror the healthcare communities we engage.
 
 
 Egypt Transplant Medical Manager will lead transplant strategy across Egypt, also will participate to/ and execute the Medical and scientific (non-promotional) in close partnership with the other functional franchise leads and in alignment with the overall franchise strategy.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Utilise strong business acumen, acting as a key strategic business partner to the organisation
 </li>
 <li>
 Initiate and drive projects to raise standards of care and change clinical practice
 </li>
 <li>
 Ability to work independently with a solutions-oriented and balanced approach to ambiguity
 </li>
 <li>
 Lead and drive rapid integrated evidence planning and execution through deep understanding of internal and external stakeholder evidence needs and robust data gaps analysis
 </li>
 <li>
 Deep therapy area expertise and product knowledge including competitor data
 </li>
 <li>
 Drive strong collaborative relationships with commercial and cross-functional teams, including marketing, value &amp; access, health economics, regulatory and clinical
 </li>
 <li>
 Cultivate and maintain relationships with external experts
 </li>
 <li>
 Drive collaborative relationships with above-country colleagues to ensure the MCO / country involvement and strategic input into global and regional plans
 </li>
 <li>
 Good understanding of the impact and evolution of healthcare systems
 </li>
 <li>
 Lead creation and implementation of medical plans &amp; implement RMMs strategy across all countries in Africa MCO.
 </li>
 <li>
 Ability to rapidly assimilate new data and integrate into the advancement in the TA.
 </li>
 <li>
 Create industry leading digital educational and scientific content that is timely, relevant, interactive and innovative.
 </li>
 <li>
 Champion the patient voice when developing and implementing medical strategies
 </li>
 <li>
 Demonstrate strong leadership influencing across networks and by coaching and mentoring members of the team
 </li>
 <li>
 Demonstrate strong leadership influencing across networks and by coaching and mentoring members of the team
 
 
 </li>
 </ul>
 
 About You
 
 
 
 
 Education
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in pharmacy, Medicine. Medical Degree or equivalent medical degree preferred, PhD or PharmD
 
 
 </li>
 </ul>
 
 Professional Experience
 
 
 
 <ul>
 <li>
 5 years Industry experience needed (5 years&rsquo; experience in Office Based Medical affairs).
 </li>
 <li>
 Good understanding of the continuum of data generation including clinical development, Real World Evidence (RWE) and data gaps analysis
 </li>
 <li>
 Ability to act independently with a solutions-oriented and balanced approach to the grey areas
 </li>
 <li>
 Excellent communication skills including driving challenging discussions&middot; Develop a good understanding of HCP communication preferences to adapt communication style and optimise use of relevant channels to suit
 </li>
 <li>
 Implement true scientific engagement journeys by bridging channel disconnect to drive ongoing engagement and grow collaborative opportunities and meaningful scientific exchange
 </li>
 <li>
 Be confident in the use of Omnichannel tools and ability to adapt to new channels
 </li>
 <li>
 Effectively and compliantly share unmet needs of HCPs and their centres with cross-functional teams to inform patient centric strategy
 
 
 </li>
 </ul>
 
 Take the Lead Values
 
 
 
 <ul>
 <li>
 Aim Higher: Focus on what matters, set high standards and move with urgency, learning from setbacks as we go to achieve higher performance.
 </li>
 <li>
 Act for Patients: Never compromise on integrity, eliminate barriers and partner with others to go faster and further for patients.
 </li>
 <li>
 Be Bold: Take thoughtful risks, seize opportunities and think beyond what's possible to accelerate our science and drive compelling growth.
 </li>
 <li>
 Lead Together: Build trust and collaborate openly on our shared goals, celebrate collective wins and foster a sense of belonging.
 
 
 </li>
 </ul>
 
 
 Why choose us?
 
 
 
 
 <ul>
 <li>
 Be part of a pioneering biopharma company where patient insights shape drug development.
 </li>
 <li>
 Lead a high-impact portfolio with bold ambitions and significant upcoming launches.
 </li>
 <li>
 Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.
 </li>
 <li>
 Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.
 </li>
 <li>
 Explore bold career paths &ndash; with opportunities to grow through scientific, leadership, and cross-functional moves.
 </li>
 </ul>
</div>

Egypt Transplant Medical Manager

<div>Job title: Head of Finance, US Vaccines
Location: Morristown, NJ / Cambridge, MA / Swiftwater, PA
About the job
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.
Role Purpose:
This role supports US Vaccines business decisions and performance analysis by preparing and reporting financial and non-financial information, budgets and forecasts for the country. The position ensures data quality, compliance and internal controls while working with various stakeholders to contribute to strategy implementation.
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:
Strategic Partnership &amp; Business Support:<ul><li>
Work with various stakeholders contributing to strategies implementation</li><li>
Monitor financial operational performance and provide accurate data and advice for decision-making</li><li>
Actively participate in business planning processes</li><li>
Contribute to strategic and business development projects</li><li>
Support business decisions through comprehensive performance analysis</li></ul>
Financial Management &amp; Reporting:<ul><li>
Prepare and report financial and non-financial information for the country/region</li><li>
Develop, manage and monitor budgets and forecasts</li><li>
Ensure data quality, compliance and internal controls</li><li>
Provide financial reporting and analysis to support business operations</li><li>
Interpret financial data to drive business insights and resource allocation</li></ul>
Stakeholder Management:<ul><li>
Collaborate with cross-functional teams and business units</li><li>
Provide financial guidance and support to regional/country leadership</li><li>
Communicate financial insights effectively to various stakeholder groups</li></ul>
About You
Required Skills &amp; Competencies
Core Technical Skills:<ul><li>
Financial Reporting and Analysis (Intermediate to Advanced)</li><li>
Planning, Budgeting and Forecasting (PBF) (Intermediate to Mastered)</li><li>
Interpreting Financial Data (Beginner to Advanced)</li><li>
Internal Control Compliance (Beginner to Advanced)</li><li>
Cash Management (Beginner to Experienced)</li><li>
Accounting (Beginner to Experienced)</li></ul>
Business &amp; Strategic Skills:<ul><li>
Risk Assessments (Beginner to Advanced)</li><li>
Stakeholder Management (Beginner to Advanced)</li><li>
Strategy Development (Beginner to Advanced)</li><li>
Business Acumen (Beginner to Advanced)</li><li>
Digital Literacy (Beginner to Advanced)</li></ul>
Career Progression Levels<ul><li>
Advanced financial analysis and reporting capabilities</li><li>
Mastered planning, budgeting and forecasting skills</li><li>
Strong stakeholder management and strategic thinking</li></ul>
Key Performance Areas<ul><li>
Effectiveness of business partnership and stakeholder relationships</li><li>
Quality and timeliness of financial reporting and analysis</li><li>
Accuracy of budgets and forecasts</li><li>
Contribution to strategic initiatives, dynamic resource allocation and business development projects</li><li>
Compliance with internal controls and regulatory requirements</li></ul>
Qualifications &amp; Experience<ul><li>
Minimum of 7 years' experience in Finance/Accounting</li><li>
Bachelor's degree in finance, Accounting, Business Administration or related field</li><li>
Professional finance qualifications (CPA, CMA, ACCA) preferred</li><li>
Experience in financial planning, analysis, and business partnering</li><li>
Strong analytical and problem-solving skills</li><li>
Excellent communication and presentation abilities</li><li>
Proficiency in financial systems and advanced Excel skills</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 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.
#GD-SP
 
#LI-SP
#LI-Onsite
#vhd
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>

Head of Finance, US Vaccines

<div><h3 class="jobSectionHeader">About Sanofi:</h3><h3 class="jobSectionHeader">
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.</h3><h3 class="jobSectionHeader">
About the Job:</h3><h3 class="jobSectionHeader">
Our Team:</h3><h3 class="jobSectionHeader">
The Africa medical Team at Sanofi is a high-performing team of medical leaders who are a trusted source of scientific and medical information and share insights; effective and innovative strategic partners to our internal and external stakeholders; and dedicated to public health. We represent diverse experiences and backgrounds which strengthen our team and mirror the healthcare communities we engage.</h3><h3 class="jobSectionHeader">
Egypt Transplant Medical Manager will lead transplant strategy across Egypt, also will participate to/ and execute the Medical and scientific (non-promotional) in close partnership with the other functional franchise leads and in alignment with the overall franchise strategy.</h3><h3 class="jobSectionHeader">
KEY RESPONSIBILITIES</h3><ul><li><h3 class="jobSectionHeader">
Utilise strong business acumen, acting as a key strategic business partner to the organisation</h3></li><li><h3 class="jobSectionHeader">
Initiate and drive projects to raise standards of care and change clinical practice</h3></li><li><h3 class="jobSectionHeader">
Ability to work independently with a solutions-oriented and balanced approach to ambiguity</h3></li><li><h3 class="jobSectionHeader">
Lead and drive rapid integrated evidence planning and execution through deep understanding of internal and external stakeholder evidence needs and robust data gaps analysis</h3></li><li><h3 class="jobSectionHeader">
Deep therapy area expertise and product knowledge including competitor data</h3></li><li><h3 class="jobSectionHeader">
Drive strong collaborative relationships with commercial and cross-functional teams, including marketing, value &amp; access, health economics, regulatory and clinical</h3></li><li><h3 class="jobSectionHeader">
Cultivate and maintain relationships with external experts</h3></li><li><h3 class="jobSectionHeader">
Drive collaborative relationships with above-country colleagues to ensure the MCO / country involvement and strategic input into global and regional plans</h3></li><li><h3 class="jobSectionHeader">
Good understanding of the impact and evolution of healthcare systems</h3></li><li><h3 class="jobSectionHeader">
Lead creation and implementation of medical plans &amp; implement RMMs strategy across all countries in Africa MCO.</h3></li><li><h3 class="jobSectionHeader">
Ability to rapidly assimilate new data and integrate into the advancement in the TA.</h3></li><li><h3 class="jobSectionHeader">
Create industry leading digital educational and scientific content that is timely, relevant, interactive and innovative.</h3></li><li><h3 class="jobSectionHeader">
Champion the patient voice when developing and implementing medical strategies</h3></li><li><h3 class="jobSectionHeader">
Demonstrate strong leadership influencing across networks and by coaching and mentoring members of the team</h3></li><li><h3 class="jobSectionHeader">
Demonstrate strong leadership influencing across networks and by coaching and mentoring members of the team</h3></li></ul><h3 class="jobSectionHeader">
About You:
</h3><h3 class="jobSectionHeader">Education</h3><ul><li><h3 class="jobSectionHeader">
Bachelor&rsquo;s degree in pharmacy, Medicine. Medical Degree or equivalent medical degree preferred, PhD or PharmD</h3></li></ul><h3 class="jobSectionHeader">
Professional Experience</h3><ul><li><h3 class="jobSectionHeader">
5 years Industry experience needed (5 years&rsquo; experience in Office Based Medical affairs).</h3></li><li><h3 class="jobSectionHeader">
Good understanding of the continuum of data generation including clinical development, Real World Evidence (RWE) and data gaps analysis</h3></li><li><h3 class="jobSectionHeader">
Ability to act independently with a solutions-oriented and balanced approach to the grey areas</h3></li><li><h3 class="jobSectionHeader">
Excellent communication skills including driving challenging discussions&middot; Develop a good understanding of HCP communication preferences to adapt communication style and optimise use of relevant channels to suit</h3></li><li><h3 class="jobSectionHeader">
Implement true scientific engagement journeys by bridging channel disconnect to drive ongoing engagement and grow collaborative opportunities and meaningful scientific exchange</h3></li><li><h3 class="jobSectionHeader">
Be confident in the use of Omnichannel tools and ability to adapt to new channels</h3></li><li><h3 class="jobSectionHeader">
Effectively and compliantly share unmet needs of HCPs and their centres with cross-functional teams to inform patient centric strategy</h3></li></ul><h3 class="jobSectionHeader">
Take the Lead Values
</h3><ul><li><h3 class="jobSectionHeader">Aim Higher: Focus on what matters, set high standards and move with urgency, learning from setbacks as we go to achieve higher performance.</h3></li><li><h3 class="jobSectionHeader">
Act for Patients: Never compromise on integrity, eliminate barriers and partner with others to go faster and further for patients.</h3></li><li><h3 class="jobSectionHeader">
Be Bold: Take thoughtful risks, seize opportunities and think beyond what's possible to accelerate our science and drive compelling growth.</h3></li><li><h3 class="jobSectionHeader">
Lead Together: Build trust and collaborate openly on our shared goals, celebrate collective wins and foster a sense of belonging.</h3></li></ul><h3 class="jobSectionHeader">
Why choose us?</h3><ul><li><h3 class="jobSectionHeader">
Be part of a pioneering biopharma company where patient insights shape drug development.</h3></li><li><h3 class="jobSectionHeader">
Lead a high-impact portfolio with bold ambitions and significant upcoming launches.</h3></li><li><h3 class="jobSectionHeader">
Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.</h3></li><li><h3 class="jobSectionHeader">
Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.</h3></li><li><h3 class="jobSectionHeader">
Explore bold career paths &ndash; with opportunities to grow through scientific, leadership, and cross-functional moves.</h3></li></ul></div>

<div>Job title: Commercial Lead &ndash; Autoimmune Type 1 Diabetes, Greater Gulf<ul><li>
Riyadh, Kingdom of Saudi Arabia</li></ul>
About the job
As Commercial Lead &ndash; Autoimmune Type 1 Diabetes within our General Medicines team, you'll drive commercial strategy and market growth for an innovative and high-priority portfolio across Saudi Arabia and the broader Gulf region. Ready to get started?
Join the team transforming how healthcare is delivered for chronic and specialty conditions worldwide. In General Medicines, you'll help drive meaningful outcomes in diabetes, transplant, and immunology &ndash; with the scale and urgency patients deserve. Based in Riyadh, you'll play a pivotal role in shaping the future of autoimmune Type 1 diabetes care across the Greater Gulf, leading cross-functional initiatives and building the partnerships that make a real difference for patients.
About Sanofi
We're an R&amp;D-driven, AI-powered biopharma company committed to improving people'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's lives.
Main responsibilities<ul><li>Develop and implement commercial strategies for the AT1D portfolio aligned with regional and global priorities; manage full P&amp;L responsibility including annual budgets, forecasts, and resource allocation to maximize return on investment.</li><li>Define and track performance metrics, identify market opportunities, and translate insights from the competitive landscape and emerging therapies into actionable plans that accelerate growth and increase market share.</li><li>Partner with market access teams to build compelling value propositions and health economic narratives, securing optimal pricing and reimbursement outcomes across Gulf markets.</li><li>Build and maintain strategic relationships with key opinion leaders, healthcare professionals, payers, and patient organizations; represent Sanofi at external meetings, conferences, and industry events.</li><li>Lead cross-functional collaboration across Medical Affairs, Regulatory, Market Access, and Marketing to deliver integrated brand strategies and co-lead product launch preparations that differentiate our offerings in the market.</li><li>Provide strategic direction and coaching to the sales organization, developing innovative customer engagement models and championing agile ways of working across the commercial team.</li><li>Ensure all commercial activities are conducted in full compliance with local regulations, industry codes, and company policies, fostering a culture of integrity throughout the organization.</li></ul>
About you<ul><li>Experience: Significant experience in progressive commercial leadership roles within the pharmaceutical or healthcare industry, with a strong track record in specialty care markets; background in diabetes is a plus. Demonstrated experience managing P&amp;L, leading cross-functional teams, and operating effectively in matrix organizations.</li><li>Soft and technical skills: Strong strategic thinking and business acumen; excellent communication, negotiation, and interpersonal skills; results-oriented with an entrepreneurial and patient-centric mindset; proven ability to engage and influence senior stakeholders across diverse functions and cultures.</li><li>Education: Bachelor's degree required; advanced degree in Business, Healthcare, or a related field preferred.</li><li>Languages: Fluent in both English and Arabic.</li><li>Proven people management experience, with the ability to inspire, coach, and develop teams.</li><li>In-depth knowledge of Greater Gulf healthcare systems, market dynamics, and regulatory and market access environments.</li><li>Willingness and ability to travel up to 60% across the Greater Gulf region and periodically to regional and global meetings.</li></ul>
Why choose us?<ul><li>Help shape the future of care for chronic and complex conditions like aT1D, Type 2 diabetes, transplant, and cardiovascular disease.</li><li>Drive meaningful impact at global scale: our medicines reach more than 100 million people each year.</li><li>Turn bold ideas into breakthrough launches, with multiple new therapies planned through 2030 and beyond.</li><li>Stretch your career in a development playground, with opportunities across functions, regions, and the entire product lifecycle.</li><li>Take the lead on one of the most exciting and fast-evolving areas in diabetes care &ndash; autoimmune Type 1 diabetes &ndash; at a pivotal moment in the treatment landscape across the Gulf.</li><li>Build your influence at the heart of a high-growth region, working at the intersection of commercial strategy, market access, and patient advocacy in a dynamic and diverse healthcare environment.</li><li>Be part of a team where entrepreneurial thinking is encouraged and your decisions have a direct, visible impact on patients and business outcomes across Saudi Arabia and neighboring Gulf markets.</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's never-been-done-before. You'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's lives? Let'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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Commercial Lead AT1D

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