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Sanofi

Sanofi est une entreprise biopharmaceutique qui innove en R&D et exploite l’IA à grande échelle pour améliorer la vie des gens et créer de la croissance à long terme. Elle se concentre sur le développement de médicaments et de vaccins innovants dans divers domaines thérapeutiques tels que l'immunologie, la neurologie, l'oncologie et les maladies rares.

<div>Job title: Logistics Lead<ul><li>
Location: Swiftwater, PA</li></ul> 
About the job
The Logistics Lead oversees a comprehensive range of logistics operations at market/above-market level. Based on scope, complexity, and organizational requirements, this role encompasses strategic management across multiple functional domains:<ul><li>
Third-Party Logistics Management - Strategic direction of external logistics partnerships</li><li>
Cost Control and Optimization - Financial stewardship and budget management</li><li>
Transportation Management - Strategic oversight of product movement to/from distribution centres</li><li>
Customs Management - Direction of import/export operations</li><li>
Warehouse Management - Governance of internal warehouse operations</li></ul>
The Logistics Lead operates in close coordination with the Head of Regional Logistics for the geography while maintaining collaborative alignment with the global logistics organization.
This role requires close collaboration with Quality, Packaging, and Engineering teams to ensure optimal material selection and distribution centre layouts are strategically designed and seamlessly implemented with external partner organization. The position demands a Sr Manager who can assess critical operational challenges, take decisive action, and successfully deliver results during the high-stakes respiratory vaccine season while supporting the broader specialty care business objectives. This would be done in coordination with the Head of Regional Logistics.
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 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 lives.
Main Responsibilities
Strategic Oversight<ul><li>
Provide comprehensive accountability for the performance, efficiency, and effectiveness of logistics and warehouse operations. This oversight will need to be done for multiple distribution sites and connections with Sanofi and CMO sites.</li></ul> 
Third-Party Logistics Management<ul><li>
Direct daily operational excellence and orchestration</li><li>
Implement strategic management of interface challenges</li><li>
Develop and maintain robust Business Continuity Plans (BCP)</li><li>
Oversee inbound process optimization</li><li>
Manage product damage resolution and returns processing through integrated claim management with i.O2C</li></ul> 
Compliance and Quality Assurance<ul><li>
Collaborate with Quality to ensure Good Distribution Practice implementation</li><li>
Lead participation in internal, external, and GDP audits</li><li>
Direct stock count procedures according to global protocols</li><li>
Leader of internal controls, audit preparation and Sox compliance and maintaining an updated and signed off packaging guide 
</li></ul> 
Supplier Relationship Management<ul><li>
Evaluate supplier strategic value and criticality to business continuity, operational excellence, and performance metrics</li><li>
Cultivate strategic supplier partnerships built on trust and mutual benefit</li><li>
Serve as interface and take leadership if routine scrums (particularly during annual vaccines respiratory season and for Specialty Care business)</li><li>
Identify cost optimization opportunities while maximizing supplier value proposition</li><li>
Coordinate supplies management of materials (packaging elements) and balancing needs with all sites and vendors.</li></ul> 
Service Level Agreement Development<ul><li>
Articulate precise business objectives and detailed service specifications</li><li>
Develop comprehensive KPIs, performance targets, and performance-based compensation structures</li><li>
Establish robust performance measurement reporting frameworks</li><li>
Implement remediation protocols for performance standard deviations</li></ul> 
Performance Management<ul><li>
Oversee VMI (Vendor Managed Inventory) customer analytics and replenishment systems where applicable</li><li>
Maintain KPI frameworks with weekly/monthly performance reviews</li><li>
Establish systematic cost control processes, including contract compliance monitoring</li><li>
Review and approve 3PL invoices while identifying continuous improvement opportunities</li></ul> 
Operational Excellence<ul><li>
Ensure alignment between best practices and 3PL core model implementation</li><li>
Engage with internal stakeholders to optimize 3PL core model application</li><li>
Drive process improvement initiatives to enhance operational efficiency</li><li>
Implement systematic performance monitoring to identify optimization opportunities</li><li>
Facilitate feedback collection from operational teams to drive continuous improvement</li></ul> 
Cost Control and Optimization<ul><li>
Develop strategic action plans for distribution cost tracking and optimization</li><li>
Implement expenditure controls with performance monitoring against approved budgets</li><li>
Engage cross-functional stakeholders (Trade, Customer Fulfilment, Commercial) to integrate distribution cost considerations into strategic decision-making regarding distribution models, route-to-market strategies, order minimums, delivery frequency, and service level commitments</li></ul>
Transportation Management<ul><li>
Direct transportation planning and execution in compliance with Sanofi protocols and Good Distribution Practice (GDP)</li><li>
Optimize cost-to-serve metrics through strategic transportation management</li></ul> 
Supplier Relationship Management<ul><li>
Develop strategic supplier partnerships built on trust and mutual benefit</li><li>
Address collaboration challenges proactively and establish service level agreements with distribution centres</li><li>
Implement KPI monitoring frameworks for distribution centre activities while driving continuous improvement</li><li>
Support audit and inspection processes with systematic improvement initiative tracking</li><li>
Establish comprehensive backup protocols and business continuity planning</li></ul> 
Customs Management (as needed and in coordination with other functions)<ul><li>
Direct import/export operations with strategic oversight</li><li>
Ensure comprehensive compliance and documentation protocols</li><li>
Implement backup personnel training to ensure operational continuity</li><li>
Develop multi-faceted Business Continuity Planning with redundant process flows</li></ul>
Warehouse Management<ul><li>
Provide strategic support for local internal distribution centre operations in compliance with regulatory requirements, Good Distribution Practice standards, and Sanofi procedures</li></ul>
The aforementioned coupled with the seasonality of vaccines&mdash;particularly during respiratory season&mdash;combined with the complexity of the specialty care business demands the ability to rapidly develop innovative solutions for multifaceted challenges. Success in this role requires thriving in a fast-paced, just-in-time environment where agility, strategic decision-making, and responsiveness to both internal and external customer needs are essential.
 About You
Required Qualifications<ul><li>
Minimum 7+ years of experience in logistics, warehouse operations management and or supply chain.</li><li>
Minimum 4+ years of experience navigating and complex external vendor relationships or partner organizations.</li><li>
Bachelor's degree from an accredited institution of higher education or equivalent work experience</li><li>
Professional-level English language proficiency</li></ul>
Preferred Qualifications<ul><li>
Onsite site logistics experience highly valued and cold chain knowledge a plus.</li><li>
Exceptional relationship management capabilities across internal and external partner organization stakeholders.</li><li>
Demonstrated collaborative leadership with proven ability to drive successful project outcomes within established timelines. Must be able to influence without authority and hold external organizations accountable.</li><li>
Extensive experience leading teams and projects within logistics, warehouse operations, and supply chain management</li><li>
Comprehensive knowledge of import/export regulations and Good Distribution Practice requirements</li></ul><ul><li>
Advanced proficiency with logistics management systems and technologies.</li><li>
APICS certification.</li></ul><ul><li>
In-depth understanding of downstream processes and pharmaceutical trade environment dynamics</li><li>
Expertise in KPI development and SLA management frameworks</li><li>
Demonstrated expertise in process improvement methodologies and change management principles</li><li>
Advanced data analytics capabilities with strong interpretive and insight generation skills</li><li>
Proven ability to operate effectively in matrix environments and adapt to dynamic business conditions</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>
Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.</li><li>
Power industry-leading performance by leveraging digital, data, and AI-driven innovation &ndash; at speed and scale.</li><li>
Transform lives worldwide by delivering life-changing treatments anywhere, anytime.</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; colour; 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-Hybrid
#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>

Logistics Lead

<div><ul><li>Job Title: Automation Engineer</li><li>
Location: Framingham, MA</li></ul> 
About the Job
Department Description: 
The MA Bio-Campus is home to Sanofi&rsquo;s digital facility which won ISPE&rsquo;s Facility of the Future and Facility of the Year 2020. As such, the Manufacturing Systems &amp; Automation group in is responsible for executing Sanofi&rsquo;s Digital Strategy to deliver innovative solutions. Focused on Digital 4.0, this group is involved in delivering digital solutions for large capital projects as well as continuous improvement and optimizing existing solutions. The group is responsible for design, implementation, support, and maintenance of digital systems aligned with site and company goals. group is responsible for maintaining stable, qualified, and highly available computing infrastructure and digital software applications. This encompasses work processes that originate with the identification of a new or revised digital systems, the design, installation, verification and validation of the system, the maintenance of the system in its commissioned/qualified/validated state and the retirement of the system at the end of its life. 
 
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 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 lives. 
Main Responsibilities:
Position Overview with Key Responsibilities: 
Key Responsibilities may differ among employees with same job title and may change over time in accordance with business needs.
This position is responsible for providing automation expertise for small to medium projects. These projects include continuous improvement and retrofit. This person will troubleshoot and support delivery of future enhancements for automation related systems.
The Automation Engineer II will be responsible for maintaining and providing technical support, ensuring availability of the automation systems for multiple manufacturing facilities. 
Additional Responsibilities include:
Leadership:<ul><li>
Providing leadership and direction to junior team members while embodying the principles of the Sanofi Global Leadership Model</li><li>
Ensuring timely issue escalation to senior management and cross-functional support teams</li><li>
Partnering with support teams i.e., Manufacturing, Quality, etc to ensure deliverables are completed to meet to production schedules</li></ul>
Automation:<ul><li>
Provide technical solutions to a wide range of process automation related design challenges. Solutions are imaginative, thorough, practical, and consistent with organization objectives</li><li>
Responsible for ensuring process equipment automation are available to support operations schedule requirements</li><li>
Managing small departmental projects and ensuring that the appropriate controls, approvals, and validation requirements are implemented</li><li>
Integrate systems and data from a variety of skidded systems, analytical equipment, and process/building control systems</li><li>
Developing robust solutions that have minimal downtime and ensure data integrity</li><li>
Contribute to the development of automation standards</li></ul>
Training /Deviations /Compliance/Safety:<ul><li>
Complying with Sanofi requirements for training</li><li>
Ensuring Inspection Readiness of assigned areas</li><li>
Overseeing completion of investigations and deviations</li><li>
Ensuring all assigned deviations and CAPA&rsquo;s are closed in a timely manner</li><li>
Ensuring that Automation documentation is compliant and inspection ready</li><li>
Participating in inspections conducted by external regulators</li><li>
Complying with requirements from Genzyme&rsquo;s Safety Program including Health and Safety regulations and OSHA requirements</li></ul>
Continuous Improvement:<ul><li>
Working collaboratively with inter-department and cross-functional teams to lead necessary changes in a timely and productive manner</li><li>
Partnering with Manufacturing to troubleshoot and drive resolution of process issues and proactively driving projects to improve manufacturing process</li><li>
Partnering with Operational Excellence to drive process improvements through Kaizens, Kanban, 5S and VSM</li></ul> 
About You 
Basic Qualifications:<ul><li> 
Bachelor&rsquo;s degree in engineering, Science or related technological field and 2+ years of experience in the automation field preferably in the life sciences</li><li>
Master's degree with 1+ years of experience in the automation field preferably in the life sciences field</li><li>
Direct experience with regulated environments (i.e. cGMP, OSHA, EPA)</li></ul> 
Preferred Qualifications:<ul><li>
Experience with DeltaV automation</li><li>
Experience with multiple computerized systems (Ignition, Werum PAS-X, PI, etc.)</li><li>
Experience with SCADA/PLC systems such as Rockwell Factory Talk/RSLogix, Honeywell</li><li>
Understanding of network infrastructure</li><li>
Experience with systems/network/validation, preferable in the chemical, pharmaceutical, foods, or other process industries is preferred</li><li>
Electrical Engineer or Chemical Engineer</li><li>
Experienced in establishment of safe practices in a cGMP environment.</li><li>
Understanding of virtual environments, VMWare, Hyper-V</li><li>
Proficient working with computer programs/applications such as Windows, VBA, MS Word, Excel, Access, etc.</li><li>
Strong organizational skills</li><li>
Self-motivated with the ability to work independently and be accountable</li><li>
Proven technical and analytical skills to quickly resolve automation system issues</li></ul> 
Special Working Conditions:<ul><li>
Required manufacturing operations support on a rotating &ldquo;on call&rdquo; 24/7 basis</li><li>
Requires working in an industrial manufacturing environment including gowning</li></ul> 
Why choose us?<ul><li>
Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.</li><li>
Power industry-leading performance by leveraging digital, data, and AI-driven innovation &ndash; at speed and scale.</li><li>
Transform lives worldwide by delivering life-changing treatments anywhere, anytime.</li><li>
Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride.</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-SG
 
#LI-GZ
#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>

Automation Engineer

<div>Job title: Case Management Specialist - Rare Hematology<ul><li>
Location: Remote, US</li></ul>
About the Job: 
Apply care coordination and case management expertise by supporting patients/families and collaboration team with services to address patient barriers to treatment. Coordinate between patients/families, healthcare providers, insurance providers, specialty pharmacy and local resources. Conduct benefit investigations, provide patient education, enroll/educate patients on/with patient support programs and coordinate outpatient services. Exceed best-in-class patient services to ensure a positive patient experience to support Sanofi business priorities. 
Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you&rsquo;ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs. 
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>
Engage patients/families to create a trusting relationship, uncover patient needs, understand challenges, and provide education and support. Manage complex issues and utilize approved resources to reduce/remove barriers as needed</li><li>
Leads the case management process, while balancing the needs of individual patients to align with the business needs/objectives of Sanofi and the Rare Blood Disorder business unit.</li><li>
Assess patients&rsquo; needs to provide for the initiation and continuation of treatment while coordinating the exchange of patient-related information to the appropriate internal and external stakeholders.</li><li>
Conduct benefit investigations and secure insurance approval for therapy, proactively plans for maintenance of coverage by working with the patients/families, healthcare providers, insurance companies and specialty pharmacies.</li><li>
Maintains comprehensive understanding of the reimbursement process, navigation of health care systems, insurance plans, payer trends, and internal and external patient assistance programs and related resources.</li><li>
Enroll patients who qualify into the appropriate financial assistance program as needed/required.</li><li>
Educates patients, family members, healthcare providers, and other collaboration members regarding insurance options, limitations, and other requirements. Also educate all stakeholders on patient support services.</li><li>
Exhibits a leadership role within the cross-functional regional team. Able to consistently identify complex patient specific issues and develop a plan to address accordingly. Establish and maintains professional and effective relationships with all internal and external stakeholders including but not limited to case management colleagues, medical, sales, market access, insurance companies, specialty pharmacies, infusion site staff and office coordinators.</li><li>
Raises own performance expectations and goals to support entrepreneurial approach to the business.</li><li>
Demonstrates and maintain high level of business acumen, understanding of Sanofi&rsquo;s business model and the role of the case manager and patient support services team in driving initiatives to meet the goals of the business unit.</li><li>
Document call details with attention to data integrity to ensure compliance and enhance our service offering</li><li>
Leverages CRM reporting tools and data analytics to make strategic decisions about their territory and prioritize patient and customer needs.</li><li>
Provide caseload coverage outside of assigned territory as needed.</li><li>
Seek coaching feedback to enhance service skills</li><li>
Ensure compliance with Sanofi policies</li></ul> 
About you: 
 
Basic Qualifications:<ul><li>
Bachelor&rsquo;s degree required</li><li>
Degree in social work or human services preferred (or equivalent professional experience in a health care or insurance setting.</li><li>
Minimum 3 years of experience in a patient facing or case management role. Experience should include but is not limited to home care management, case management review, utilization review, social service support, insurance reimbursement and patient advocacy.</li></ul>
Preferred Qualifications:<ul><li>
Industry experience preferred.</li><li>
Spanish language fluency highly preferred</li><li>
In-depth understanding of health insurance benefits, relevant state and federal laws and insurance regulations.</li><li>
Developed communication, mediation, and problem solving-skills</li><li>
Experience with engaging patients and caregivers with rare/chronic conditions</li><li>
Ability to identify and handle sensitive issues with opposing opinions, work independently and lead projects as needed.</li><li>
Excellent attention to detail and ability to multi-task in a fast-paced environment</li><li>
Experience with Salesforce CRM preferred</li><li>
Proficient with MS Word, MS Excel, and MS PowerPoint</li><li>
Working hours may vary based on business needs and team coverage</li><li>
This schedule can vary between 8:30 am - 7:00 pm EST (hours to be determined before hiring)</li></ul> 
Why Choose Us?<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>
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-SG
 
#LI-GZ
#LI-Remote
#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>

Case Management Specialist - Rare Hematology (Spanish-Speaking)

<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>About the job
As Quantitative Pharmacology Project Expert within our Translational Medicine Unit, you&rsquo;ll lead pharmacology programs supporting global R&amp;D projects from research phase or in-licensing through registration. Ready to get started?
Based in Germany, you'll join our R&amp;D organization where we leverage deep scientific expertise and cutting-edge pharmacology to advance our innovative pipeline. This position offers the opportunity to develop and monitor the execution of pharmacology strategies in global R&amp;D projects.
Main responsibilities:<ul><li>
Develop the strategy and monitor the execution of the Quantitative Pharmacology programs of the Translational Medicine Unit to support in-licensing, global research &amp; development projects and the registration of products.</li><li>
Lead global Translational Medicine and/or Quantitative Pharmacology sub-teams. Monitor related activities, e.g., modelling &amp; simulation, assay development, development of non-clinical and clinical study designs. Drive the selection of dose and dosing regimen, and de-risk the potential of drug-drug interactions.</li><li>
Development and/or review of protocols, analysis plans, and study reports; review and/or conduct of PK, PK/PD, population PK, population PK/PD, and/or PBPK analyses.</li><li>
Provide input to the preparation of regulatory documents and participate in interactions with health authority at key milestones.</li></ul>
About you
Experience:<ul><li>
Experience in pharmaceutical development.</li><li>
Experience with regulatory interactions (especially FDA and EMA) and submissions.</li><li>
Experience in pharmacokinetic/statistical analysis of clinical data with common software packages (e.g. Phoenix).</li><li>
Experience in software for physiology-based PK modelling (preferably PK-Sim or SimCyp), and population modeling for analyzing PK/PD data (NonMem, R) would be of advantage.</li></ul>
Education:<ul><li>
PhD in pharmacokinetics, pharmacometrics, clinical pharmacology, or other suitable post-graduate qualifications.</li></ul>
Languages:<ul><li>
Fluency in English required.</li></ul>
Why choose us?<ul><li>
Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.</li><li>
Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.</li><li>
Help improve the lives of millions of people globally by making drug development quicker and more effective.</li><li>
Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs.</li><li>
Accelerate your professional development with structured career paths designed for both scientific and leadership advancement. Grow in ways you never imagined through bold moves that stretch your potential, cross moves into other business areas, and short-term gigs that build your scientific expertise.
</li><li>Enjoy outstanding benefits, including flexible working options, comprehensive healthcare, and well-being programs designed to help you thrive.</li></ul>
#LI-Hybrid
#PharmaceuticalDevelopment
#Pharmacometrics
#QuantitativePharmacology
#Sanofi
#SanofiCareers
#PursueProgress
#DiscoverExtraordinary
#WeAreSanofi
#IgnitingPotential</div>

Senior Principal Scientist, Clinical Expert in Pharmacokinetics - all genders

<div>About the job
Within the Synthetics platform of Sanofi&rsquo;s Global CMC organization, we are offering a position for a senior scientist within the DP Design team in Frankfurt which has an interdisciplinary scientific scope covering of formulation, biopharmacy and analytics. As part of the team you will support the development of new medications from research to clinical testing by developing pre-clinical and clinical formulations in close interaction with global CMC and project teams. 
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>
Act as formulation expert and representative in global R&amp;D project teams for pre-clinical and clinical formulation development</li><li>
Provide formulation strategies/solutions and early biopharmaceutical risk evaluations to project teams enabling proper candidate profiling, selection and development</li><li>
Responsible for the supply of various pre-clinical studies</li><li>
Evaluation, interpretation and presentation of data and Progress</li><li>
Manage close interaction and exchange with global CMC functions, pharmacokinetics, pre-clinical safety, medicinal chemistry and the therapeutic areas</li><li>
Contribute to the continuous evolution of methods, analytics, way of working and formulation strategies as part of the DP Design team</li><li>
Laboratory management &ndash; including equipment and documentation</li><li>
Instruction and training of technicians</li></ul>
About you<ul><li>
Ph.D. in pharmaceutical or related natural sciences</li><li>
Strong scientific background in formulation development</li><li>
Experience in biopharmaceutical experimentation and modelling</li><li>
German: spoken with confidence to ensure proper communication with lab staff</li><li>
English: excellent written/oral communication and presentation skills</li></ul> 
Why choose us?
Join the engine of Sanofi&rsquo;s mission &mdash; where deep immunoscience meets bold, AI-powered research. In R&amp;D, you&rsquo;ll drive breakthroughs that could turn the impossible into possible for millions. 
<ul><li>
Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.</li><li>
Help improve the lives of millions of people globally by making drug development quicker and more effective.</li><li>
Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs.</li><li>
Achieve genuine work-life balance in a supportive R&amp;D environment.</li></ul>
#LI-Onsite
#PreclinicalFormulation
#ClinicalFormulation
#DrugProduct
#Sanofi
#SanofiCareers
#PursueProgress
#DiscoverExtraordinary
#WeAreSanofi
#IgnitingPotential</div>

Senior Scientist Drug Product - all genders (limited contract for 12 months)

Join Sanofi and explore 17   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.