Health Insurance

Life Insurance

Work From Home

Flexible Working

Large

We are Sanofi, an innovative global healthcare company. We chase 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.

Science & Healthcare

Sanofi

Pharmaceuticals

You should have 2+ years in clinical statistical programming, vaccine experience, SAS skills, CDISC SDTM/ADaM knowledge, teamwork, organization, and critical thinking capabilities.

You will program statistical deliverables, review study documents, ensure compliance with CDISC standards, and contribute to quality control and integrated clinical database programming.

Data

Research & Development

Hyderabad

<div><h2 class="jobSectionHeader"><b>Job title: Stat Programmer (Vaccine)</b></h2><p></p><h2 class="jobSectionHeader"><b>
About the job</b></h2><p></p><p>
Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. Build a career and you can be part of transforming our business while helping to change millions of lives. Ready? As a Statistical Programmer within our Hyderabad Hub, you&rsquo;ll be part of a performing team, delivering biostatistics and programming activities throughout the Vaccines R&amp;D value chain (PreClinical, Clinical, Translational, CMC) with our Vaccines Global Biostatistical Sciences team. We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.</p><p></p><h2 class="jobSectionHeader"><b>
Main responsibilities:</b></h2><p></p><ul><li>Perform programming activities for all statistical deliverables (i.e.: SDTM, ADaM, Tables Listings and Figures (TLF)) for various analyses within a study (e.g.: interim/final analyses, internal or external data monitoring committees, statistical surveillance)</li><li>Review and provide feedback on study documents such as Case Report Form, Statistical Analysis Plan (SAP), mock TLFs, programming specifications</li><li>Write or review programming specifications for the SDTM/ADaM/TLFs to fulfil the study objectives</li><li>Deliver compliant CDISC data package with all relevant documentation (ie: aCRF, reviewers guide, define.xml) fulfilling Heath Authorities expectations</li><li>Ensure TLF&rsquo;s format fulfil the requirements of targeted publishing (i.e.: clinical study report, publication, Transparency like Eudract, CTT.gov, lay summaries,...)</li><li>Contribute to quality control for statistical programming deliverables and complete the associated documentation</li><li>Might contribute to core integrated clinical database programming, pooling across several studies within an asset</li><li>Ensure compliance to SOP's, standards, and guidelines.</li></ul><p></p><h2 class="jobSectionHeader"><b>
About You</b></h2><p></p><ul><li><b>Experience: Should Have at 2 + Years of experience in clinical statistical programming.</b></li><li><b>Should Have experience on vaccine therapeutic area in clinical statistical programming</b>.</li><li>Soft Skill &amp; Technical Skill: technical skills in SAS/BASE, STAT, MACRO</li><li>Experience on programming CDISC SDTM/ADaM datasets according to existing specifications (including running and resolving P21 compliance checks) is must.</li><li>Ability to work according to existing specifications.</li><li>Demonstrate an understanding of processes associated with clinical trials and statistics.</li><li>Demonstrate interpersonal skills necessary for effective teamwork.</li><li>Demonstrate ability to organize multiple work assignments and establish priorities.</li><li>Demonstrate critical thinking skills beyond simply following directions or specifications</li></ul></div>

Job title: Stat Programmer (Vaccine)
About the job
Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. Build a career and you can be part of transforming our business while helping to change millions of lives. Ready? As a Statistical Programmer within our Hyderabad Hub, you’ll be part of a performing team, delivering biostatistics and programming activities throughout the Vaccines R&D value chain (PreClinical, Clinical, Translational, CMC) with our Vaccines Global Biostatistical Sciences team. We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
Main responsibilities:Perform programming activities for all statistical deliverables (i.e.: SDTM, ADaM, Tables Listings and Figures (TLF)) for various analyses within a study (e.g.: interim/final analyses, internal or external data monitoring committees, statistical surveillance)Review and provide feedback on study documents such as Case Report Form, Statistical Analysis Plan (SAP), mock TLFs, programming specificationsWrite or review programming specifications for the SDTM/ADaM/TLFs to fulfil the study objectivesDeliver compliant CDISC data package with all relevant documentation (ie: aCRF, reviewers guide, define.xml) fulfilling Heath Authorities expectationsEnsure TLF’s format fulfil the requirements of targeted publishing (i.e.: clinical study report, publication, Transparency like Eudract, CTT.gov, lay summaries,...)Contribute to quality control for statistical programming deliverables and complete the associated documentationMight contribute to core integrated clinical database programming, pooling across several studies within an assetEnsure compliance to SOP's, standards, and guidelines.
About YouExperience: Should Have at 2 + Years of experience in clinical statistical programming.Should Have experience on vaccine therapeutic area in clinical statistical programming.Soft Skill & Technical Skill: technical skills in SAS/BASE, STAT, MACROExperience on programming CDISC SDTM/ADaM datasets according to existing specifications (including running and resolving P21 compliance checks) is must.Ability to work according to existing specifications.Demonstrate an understanding of processes associated with clinical trials and statistics.Demonstrate interpersonal skills necessary for effective teamwork.Demonstrate ability to organize multiple work assignments and establish priorities.Demonstrate critical thinking skills beyond simply following directions or specifications

Stats Programmer (Vaccine) - Sanofi

<div>
 <h2 class="jobSectionHeader"><b>Job title: Stat Programmer (Vaccine)</b></h2>
 <p></p>
 <h2 class="jobSectionHeader"><b> About the job</b></h2>
 <p></p>
 <p>Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. Build a career and you can be part of transforming our business while helping to change millions of lives. Ready? As a Statistical Programmer within our Hyderabad Hub, you’ll be part of a performing team, delivering biostatistics and programming activities throughout the Vaccines R&amp;D value chain (PreClinical, Clinical, Translational, CMC) with our Vaccines Global Biostatistical Sciences team. We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.</p>
 <p></p>
 <h2 class="jobSectionHeader"><b> Main responsibilities:</b></h2>
 <p></p>
 <ul>
  <li>Perform programming activities for all statistical deliverables (i.e.: SDTM, ADaM, Tables Listings and Figures (TLF)) for various analyses within a study (e.g.: interim/final analyses, internal or external data monitoring committees, statistical surveillance)</li>
  <li>Review and provide feedback on study documents such as Case Report Form, Statistical Analysis Plan (SAP), mock TLFs, programming specifications</li>
  <li>Write or review programming specifications for the SDTM/ADaM/TLFs to fulfil the study objectives</li>
  <li>Deliver compliant CDISC data package with all relevant documentation (ie: aCRF, reviewers guide, define.xml) fulfilling Heath Authorities expectations</li>
  <li>Ensure TLF’s format fulfil the requirements of targeted publishing (i.e.: clinical study report, publication, Transparency like Eudract, CTT.gov, lay summaries,...)</li>
  <li>Contribute to quality control for statistical programming deliverables and complete the associated documentation</li>
  <li>Might contribute to core integrated clinical database programming, pooling across several studies within an asset</li>
  <li>Ensure compliance to SOP's, standards, and guidelines.</li>
 </ul>
 <p></p>
 <h2 class="jobSectionHeader"><b> About You</b></h2>
 <p></p>
 <ul>
  <li><b>Experience: Should Have at 2 + Years of experience in clinical statistical programming.</b></li>
  <li><b>Should Have experience on vaccine therapeutic area in clinical statistical programming</b>.</li>
  <li>Soft Skill &amp; Technical Skill: technical skills in SAS/BASE, STAT, MACRO</li>
  <li>Experience on programming CDISC SDTM/ADaM datasets according to existing specifications (including running and resolving P21 compliance checks) is must.</li>
  <li>Ability to work according to existing specifications.</li>
  <li>Demonstrate an understanding of processes associated with clinical trials and statistics.</li>
  <li>Demonstrate interpersonal skills necessary for effective teamwork.</li>
  <li>Demonstrate ability to organize multiple work assignments and establish priorities.</li>
  <li>Demonstrate critical thinking skills beyond simply following directions or specifications</li>
 </ul>
</div>

Stats Programmer (Vaccine)

You need 10+ years in digital product delivery, preferably in biopharma, Agile experience, strong financial acumen, and the ability to lead cross-functional teams and initiatives effectively.

You will lead a diverse team, develop digital product strategies, oversee product delivery, facilitate Agile processes, measure business impact, and drive user adoption and satisfaction.

Software Engineering

Product

Lyon

<div><div><div><div><p><i>Le contenu du poste est libell&eacute; en anglais car il n&eacute;cessite de nombreuses interactions avec nos filiales &agrave; l&rsquo;international, l'anglais &eacute;tant la langue de travail.</i></p></div><p></p><div><p><i><br>
This job</i><i> </i><i>offer</i><i> is </i><i>accessible</i><i> to all, regardless of gender.</i></p></div><p></p><p><b>
Job title</b>:<i> </i><i>Product Line </i><i>Owner</i><i> Launch Engine</i></p></div><div><ul><li><i>
Location</i><i>: Lyon</i></li></ul></div><p></p><div><div><div><h1 class="jobSectionHeader"><b><i>
About the job</i></b></h1></div></div><p></p><div><div><p><br>
At Sanofi, we&rsquo;re committed to transform the practice of medicine through break-through science. Within Sanofi, Manufacturing &amp; Supply (M&amp;S) is the bridge between Science and Patients, ensuring all patients get their dose reliably, that new medicines are launched faster to cover unmet needs and that they can be delivered affordably across the globe. At Sanofi we are convinced that Manufacturing is, and must in the future increasingly be, a competitive advantage and that digital unlocks every next step in that journey. Join our Digital M&amp;S Accelerator team as Product Line Owner and you can help make it happen.</p></div><p></p><div><p><br>
Your job? As Product Line Owner for Launch Engine, you will join a dynamic team committed to solve Sanofi M&amp;S most challenging opportunities with digital capabilities while spearheading Sanofi&rsquo;s digital transformation. This leadership role involves developing digital product strategies, ensuring successful delivery through Agile methodologies, and driving business impact. You will play a critical role to ensure that we build a great team of highly talented and motivated Product Owners, in a fun and high intensity culture while executing on a robust strategy and roadmap to deliver high value across our portfolio of Digital Products.</p></div><p></p><div><p><br>
Sanofi Manufacturing &amp; Supply is the most extraordinary playground you can imagine. The world of drug development and advanced manufacturing with opportunities for real-world AI is one of the most fascinating places to be in digital today and biomanufacturing puts an additional twist of challenge working with biological living processes and saving people&rsquo;s lives.</p></div><p></p><div><p><br>
You will deliver capabilities to our 12 blockbuster Launch teams and 40 factories spread across five continents, working across both R&amp;D and M&amp;S. You will work with real-time IOT data from hundreds of manufacturing lines with leading edge production and laboratory equipment. You will help secure one of the strongest new treatment pipelines in the biopharma industry. And you will serve thousands of extraordinary scientists, process engineers, manufacturing engineers, manufacturing operators and quality experts who are convinced that digital is the path to become a best-in-class organization.</p></div><p></p><div><p><br>
We have established the Digital M&amp;S Accelerator as a dedicated agile organization to deliver High Value Digital Products focused primarily on accelerating launches and creating best in class digitalized factories we call Lighthouses. The ambition is first to secure the pipeline of new treatment launches, successfully launching yearly 3 to 5 new blockbuster medicines (peak yearly revenue of 1 billion euros) where delays have multi-million euros impact and second to deliver manufacturing performance driving cost of goods reduction of more than 500 million euros over the next five years.</p></div><p></p><div><p><br>
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?</p></div><p></p><div><h1 class="jobSectionHeader"><b><i><br>
About Growing with us</i></b></h1></div><p></p><div><p>
In this role you will own and deliver a portfolio of new innovative Digital Products. Your key objective is to secure the successful launches of Sanofi&rsquo;s pipeline by providing digital capabilities to ensure right-first-time operations and agility in accelerating launches.</p></div><p></p><div><p><br>
You will be empowered to build digital capabilities that disrupt current manufacturing and new medicine launch practices. You will be expected not just to enable but to modernize, automate or eliminate activities not creating value by leveraging digital, data and AI technologies:</p></div><div><ul><li>
Recruit, lead, develop and support a diverse and talented team of Product Owners in partnership with the P&amp;C function</li><li>
Collaborate with Global R&amp;D/M&amp;S leaders and Digital M&amp;S MSAT &amp; Engineering Product Line to co-develop digital product strategies and roadmaps</li><li>
Own the vision and communications of the Products roadmap and expected outcomes</li><li>
Ensure seamless integration of Accelerator Products in the broader ecosystem of R&amp;D and M&amp;S digital capabilities</li><li>
Lead cross-functional teams, including product owners, software engineers, data engineers, data scientists, UX/UI experts, and analysts</li><li>
Oversee digital product delivery from inception to launch and continuous improvement, ensuring alignment with R&amp;D and M&amp;S's strategic objectives and achievement of outcomes</li><li>
Facilitate Agile development processes to deliver high-quality capabilities fast. Act as a mediator between stakeholders, users, and technology teams</li><li>
Deliver Products that are easy to adopt and use, contribute to roll-out across launch teams and factories and constantly advocate for improved usage and user satisfaction</li><li>
Measure and report the business impact of digital products to executives</li><li>
Inspire the team, raise the ambition and bring a unique vision and perspective for what is possible</li></ul></div></div><p></p><div><div><h1 class="jobSectionHeader"><b><i>
About you</i></b></h1></div><div><p><br>
<br>
<b>Experience:</b></p></div><div><ul><li>
10+ years of experience working in Digital Product delivery as a product owner, product line owner or product manager, preferably with experience in CMC, industrial development or manufacturing</li><li>
Experience in a biopharma or biotech company is a strong plus</li><li>
Experience with Agile and Digital transformation in complex, international environments</li></ul></div><p></p><div><p><b>
Soft skills</b>:</p></div><div><ul><li>
Excellent influencing, communication &amp; presenting skills, including with executive stakeholders</li><li>
Proven business sense, strong financial acumen, ability to take decisions, think strategically and partner with business/other teams</li><li>
Proven ability to lead strategic Digital initiatives at scale, translating business requirements into technology-driven innovation and solution design while delivering multiple transformative digital products in parallel</li><li>
Expertise in leading cross-functional teams to create Digital strategies and implementation roadmaps. Distinctive focus on solution objectives and application of product methodologies (design thinking, iteration, fast fail, etc.)</li><li>
Solid knowledge and experience of Lean &amp; Agile practices, UX/UI and Application Design &amp; Integration</li><li>
Curiosity, creativity, sense of detail, first principles and &ldquo;get things done&rdquo; mindset</li></ul></div></div><p></p><div><div><p><b><br>
Technical skills</b>:</p></div><div><ul><li>
Solid knowledge of Lean or Agile practices, User Experience &amp; Application Design</li><li>
Knowledge of biopharma process engineering is a strong plus</li></ul></div><p></p><div><p><b>
Education:</b></p></div><div><ul><li>
Master&rsquo;s degree in computer science or equivalent scientific field, with 5+ years of experience in product management, preferably in healthcare or biotech</li></ul></div><p></p><div><h1 class="jobSectionHeader"><b><i><br>
Why choose us?</i></b></h1></div><p></p><div><p><br>
We provide a highly collaborative environment, with an opportunity to work with a world class team. You will be able to:</p></div><div><ul><li>
Learn what it takes to make a service with a truly global reach</li><li>
Be part of an organization that values diversity, inclusion, and the richness of different backgrounds and experiences</li><li>
Engage in meaningful work that combines the challenges of the medical, pharma, environmental matters and technical fields, offering abundant opportunities for professional growth and impact</li><li>
Contribute to a company that is not only a leader in healthcare but also a pioneer in digital transformation, shaping the future of global health</li></ul></div></div></div></div><p></p><div><div><p><b>
Pursue</b> <i>Progress</i>. <b>Discover </b><i>Extraordinary</i>.</p></div></div><p></p><div><p>
Progress doesn&rsquo;t happen without people &ndash; people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let&rsquo;s pursue progress. And let&rsquo;s discover extraordinary together.</p></div><p></p><div><p><br>
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.</p></div><div><p><br>
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!</p><p></p><div><p><b>
#LI-FRA</b></p></div><div><p><b>
#LI-Hybrid</b></p></div></div></div>

Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec nos filiales à l’international, l'anglais étant la langue de travail.
This job offer is accessible to all, regardless of gender.
Job title: Product Line Owner Launch Engine
Location: Lyon
About the job
At Sanofi, we’re committed to transform the practice of medicine through break-through science. Within Sanofi, Manufacturing & Supply (M&S) is the bridge between Science and Patients, ensuring all patients get their dose reliably, that new medicines are launched faster to cover unmet needs and that they can be delivered affordably across the globe. At Sanofi we are convinced that Manufacturing is, and must in the future increasingly be, a competitive advantage and that digital unlocks every next step in that journey. Join our Digital M&S Accelerator team as Product Line Owner and you can help make it happen.
Your job? As Product Line Owner for Launch Engine, you will join a dynamic team committed to solve Sanofi M&S most challenging opportunities with digital capabilities while spearheading Sanofi’s digital transformation. This leadership role involves developing digital product strategies, ensuring successful delivery through Agile methodologies, and driving business impact. You will play a critical role to ensure that we build a great team of highly talented and motivated Product Owners, in a fun and high intensity culture while executing on a robust strategy and roadmap to deliver high value across our portfolio of Digital Products.
Sanofi Manufacturing & Supply is the most extraordinary playground you can imagine. The world of drug development and advanced manufacturing with opportunities for real-world AI is one of the most fascinating places to be in digital today and biomanufacturing puts an additional twist of challenge working with biological living processes and saving people’s lives.
You will deliver capabilities to our 12 blockbuster Launch teams and 40 factories spread across five continents, working across both R&D and M&S. You will work with real-time IOT data from hundreds of manufacturing lines with leading edge production and laboratory equipment. You will help secure one of the strongest new treatment pipelines in the biopharma industry. And you will serve thousands of extraordinary scientists, process engineers, manufacturing engineers, manufacturing operators and quality experts who are convinced that digital is the path to become a best-in-class organization.
We have established the Digital M&S Accelerator as a dedicated agile organization to deliver High Value Digital Products focused primarily on accelerating launches and creating best in class digitalized factories we call Lighthouses. The ambition is first to secure the pipeline of new treatment launches, successfully launching yearly 3 to 5 new blockbuster medicines (peak yearly revenue of 1 billion euros) where delays have multi-million euros impact and second to deliver manufacturing performance driving cost of goods reduction of more than 500 million euros over the next five years.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
About Growing with us
In this role you will own and deliver a portfolio of new innovative Digital Products. Your key objective is to secure the successful launches of Sanofi’s pipeline by providing digital capabilities to ensure right-first-time operations and agility in accelerating launches.
You will be empowered to build digital capabilities that disrupt current manufacturing and new medicine launch practices. You will be expected not just to enable but to modernize, automate or eliminate activities not creating value by leveraging digital, data and AI technologies:
Recruit, lead, develop and support a diverse and talented team of Product Owners in partnership with the P&C function
Collaborate with Global R&D/M&S leaders and Digital M&S MSAT & Engineering Product Line to co-develop digital product strategies and roadmaps
Own the vision and communications of the Products roadmap and expected outcomes
Ensure seamless integration of Accelerator Products in the broader ecosystem of R&D and M&S digital capabilities
Lead cross-functional teams, including product owners, software engineers, data engineers, data scientists, UX/UI experts, and analysts
Oversee digital product delivery from inception to launch and continuous improvement, ensuring alignment with R&D and M&S's strategic objectives and achievement of outcomes
Facilitate Agile development processes to deliver high-quality capabilities fast. Act as a mediator between stakeholders, users, and technology teams
Deliver Products that are easy to adopt and use, contribute to roll-out across launch teams and factories and constantly advocate for improved usage and user satisfaction
Measure and report the business impact of digital products to executives
Inspire the team, raise the ambition and bring a unique vision and perspective for what is possible
About you

Experience:
10+ years of experience working in Digital Product delivery as a product owner, product line owner or product manager, preferably with experience in CMC, industrial development or manufacturing
Experience in a biopharma or biotech company is a strong plus
Experience with Agile and Digital transformation in complex, international environments
Soft skills:
Excellent influencing, communication & presenting skills, including with executive stakeholders
Proven business sense, strong financial acumen, ability to take decisions, think strategically and partner with business/other teams
Proven ability to lead strategic Digital initiatives at scale, translating business requirements into technology-driven innovation and solution design while delivering multiple transformative digital products in parallel
Expertise in leading cross-functional teams to create Digital strategies and implementation roadmaps. Distinctive focus on solution objectives and application of product methodologies (design thinking, iteration, fast fail, etc.)
Solid knowledge and experience of Lean & Agile practices, UX/UI and Application Design & Integration
Curiosity, creativity, sense of detail, first principles and “get things done” mindset
Technical skills:
Solid knowledge of Lean or Agile practices, User Experience & Application Design
Knowledge of biopharma process engineering is a strong plus
Education:
Master’s degree in computer science or equivalent scientific field, with 5+ years of experience in product management, preferably in healthcare or biotech
Why choose us?
We provide a highly collaborative environment, with an opportunity to work with a world class team. You will be able to:
Learn what it takes to make a service with a truly global reach
Be part of an organization that values diversity, inclusion, and the richness of different backgrounds and experiences
Engage in meaningful work that combines the challenges of the medical, pharma, environmental matters and technical fields, offering abundant opportunities for professional growth and impact
Contribute to a company that is not only a leader in healthcare but also a pioneer in digital transformation, shaping the future of global health
Pursue Progress. Discover Extraordinary.
Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary 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, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
#LI-FRA
#LI-Hybrid

Digital Product Line Owner - Sanofi

Digital Product Line Owner

You need 2-6 years of graphic design experience, strong skills in Adobe suite, excellent communication, and a background in healthcare/science. Must manage time well and follow brand guidelines.

You will design various educational and promotional materials, collaborate with teams, manage project timelines, provide technical support, and stay updated on design technologies and best practices.

Healthcare

Design

<div><p><b>Our Team:</b></p><p><i>
Brief introduction of the department, team, purpose, and missions. Highlight what is unique to your team.</i></p><p>
Sanofi Business Operations: Medical &amp; Commercial (SBO: M&amp;C) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&amp;D, Data &amp; Digital functions. SBO strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally.</p><p></p><p><b><br>
Main responsibilities:</b></p><p><i>
The overall purpose and main responsibilities are listed below:</i></p><p><i>
Design and produce creative deliverables like medical training and educational videos, quarterly insight videos, explainer videos, infographic animation, video publication articles, video editing, sound editing, removing background noise from audio clips, promotional videos, animated icons, PowerPoint slide decks, scientific posters, redrawing scientific images, interactive PPTs, Infographics, newsletters, e-mailers, flyers, brochures, handouts and e-learning modules as per the provided guidelines and specifications</i></p><br>
<p></p><ul><li>
People: (1) Maintain effective relationships with Content Enhancement team and Scientific Writers in SBO (and globally stakeholders, based on the project requirement) with an end objective to ensure preparing in scientific communication materials are developed to meet stakeholder requirements.</li><li>
Performance: (1) Work on business-critical deliverables, primarily on publication materials (medical training and educational videos, quarterly insight videos, explainer videos, infographic animation, video publication articles, video editing, sound editing, removing background noise from audio clips, promotional videos, and animated icons) following the provided guidelines (2) Extend support to work on digital and interactive deliverables (e-learning modules, scientific posters, newsletters, annual reports, e-mailers, patient education materials and other deliverables) based on the need.</li><li>
Process: (1) Collaborate primarily with other graphic designers and SBO Scientific Writers to understand better on received project specific requirements and deliver the received requests on agreed time with good quality (2) Provide technical support and guidance to other graphic designers, when needed (3) Proactively communicating and flagging issues to Team Lead on project timelines, any issues with the inputs received from Scientific Writers (4) Prioritize and manage assigned projects; adhering to the defined quality and delivering on time following the provided specifications from the stakeholder (5)Designing and setting up new templates adhering to brand guidelines and manage the continuity (6) Actively participate in team meetings and provide suggestions based on the need for the team (7) Sharing best practices or any new learnings to the team (8) Showing flexibility to meet project demands to deliver the output on-time. (9) Upskill to enhance the content enhancement deliverables (10) Indulge in self-learning in order to keep yourself updated with the latest developments in technologies required for the execution of work</li></ul><p></p><p><br>
About you</p><p></p><ul><li><b><br>
Experience</b>: <i>&gt;2 to &lt;=6 years of experience in graphic design, video creation, and new media</i></li></ul><p><i>
Desirable experience in pharmaceuticals / healthcare industry and scientific context mediation</i></p><ul><li><b>
Soft skills</b>: <i>Stakeholder management; communication skills; and ability to work independently and within a team environment</i></li><li><b>
Technical skills</b>:</li><li><i>
Must have strong hands-on experience with Adobe After Effects, Adobe Premiere Pro, Adobe Photoshop, Adobe Illustrator, Adobe InDesign and Microsoft PowerPoint.</i></li><li><i>
Ability to translate complex information in to video or other allied easy ways to communicate visually</i></li><li><i>
Ability to think creatively, aesthetically, independently and having good knowledge on all the graphic and current design trends</i></li><li><i>
Experience / knowledge following brand guidelines while working on deliverables and preparing templates</i></li><li><i>
Strong organizational and time management skills to effectively manage completing work activities.</i></li><li><i>
Good communication skills both verbal and written.</i></li><li><i>
Should be able to communicate clearly and effectively</i></li><li><b>
Education</b>: <i>Graduate or postgraduate in any stream. Primarily in graphic design or art with focus on visualization of scientific content</i></li><li><b>
Languages</b>: <i>Excellent knowledge of English language (spoken and written)</i></li></ul></div>

Our Team:
Brief introduction of the department, team, purpose, and missions. Highlight what is unique to your team.
Sanofi Business Operations: Medical & Commercial (SBO: M&C) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. SBO strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally.
Main responsibilities:
The overall purpose and main responsibilities are listed below:
Design and produce creative deliverables like medical training and educational videos, quarterly insight videos, explainer videos, infographic animation, video publication articles, video editing, sound editing, removing background noise from audio clips, promotional videos, animated icons, PowerPoint slide decks, scientific posters, redrawing scientific images, interactive PPTs, Infographics, newsletters, e-mailers, flyers, brochures, handouts and e-learning modules as per the provided guidelines and specifications

People: (1) Maintain effective relationships with Content Enhancement team and Scientific Writers in SBO (and globally stakeholders, based on the project requirement) with an end objective to ensure preparing in scientific communication materials are developed to meet stakeholder requirements.
Performance: (1) Work on business-critical deliverables, primarily on publication materials (medical training and educational videos, quarterly insight videos, explainer videos, infographic animation, video publication articles, video editing, sound editing, removing background noise from audio clips, promotional videos, and animated icons) following the provided guidelines (2) Extend support to work on digital and interactive deliverables (e-learning modules, scientific posters, newsletters, annual reports, e-mailers, patient education materials and other deliverables) based on the need.
Process: (1) Collaborate primarily with other graphic designers and SBO Scientific Writers to understand better on received project specific requirements and deliver the received requests on agreed time with good quality (2) Provide technical support and guidance to other graphic designers, when needed (3) Proactively communicating and flagging issues to Team Lead on project timelines, any issues with the inputs received from Scientific Writers (4) Prioritize and manage assigned projects; adhering to the defined quality and delivering on time following the provided specifications from the stakeholder (5)Designing and setting up new templates adhering to brand guidelines and manage the continuity (6) Actively participate in team meetings and provide suggestions based on the need for the team (7) Sharing best practices or any new learnings to the team (8) Showing flexibility to meet project demands to deliver the output on-time. (9) Upskill to enhance the content enhancement deliverables (10) Indulge in self-learning in order to keep yourself updated with the latest developments in technologies required for the execution of work
About you
Experience: >2 to <=6 years of experience in graphic design, video creation, and new media
Desirable experience in pharmaceuticals / healthcare industry and scientific context mediation
Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment
Technical skills:
Must have strong hands-on experience with Adobe After Effects, Adobe Premiere Pro, Adobe Photoshop, Adobe Illustrator, Adobe InDesign and Microsoft PowerPoint.
Ability to translate complex information in to video or other allied easy ways to communicate visually
Ability to think creatively, aesthetically, independently and having good knowledge on all the graphic and current design trends
Experience / knowledge following brand guidelines while working on deliverables and preparing templates
Strong organizational and time management skills to effectively manage completing work activities.
Good communication skills both verbal and written.
Should be able to communicate clearly and effectively
Education: Graduate or postgraduate in any stream. Primarily in graphic design or art with focus on visualization of scientific content
Languages: Excellent knowledge of English language (spoken and written)

Graphic Designer - Sanofi

Graphic Designer

You need 5+ years in pharmacovigilance, strong leadership in global teams, CHC experience, operational excellence, regulatory knowledge, and a higher degree in business or law.

You will develop and manage Pharmacovigilance Agreements, lead projects, foster partnerships, support licensing strategies, and drive collaboration across stakeholders to ensure effective PV processes.

Legal

<div><p><b>Job title:</b> Pharmacovigilance Agreements Expert</p><p></p><p><b>
Location: </b>Hyderabad</p><p><b>
% of travel expected: </b>Travel required as per business need</p><p><b>
Job type:</b> Permanent and Full time</p><p></p><p><b>
About the job</b></p><p></p><p><b>
Our Team:</b></p><p>
At Sanofi Consumer Healthcare, we have one overarching mission - to work passionately, challenging ourselves and our industry every day, to build a healthier future by helping people, help themselves, bringing &ldquo;Health in Your Hands&rdquo;. Our teams are building trusted &amp; loved brands that connect with hundreds of millions of consumers worldwide, enabling better self-care for individuals and communities, while also contributing to a healthier planet. To fulfil this mission, we are embarking our consumers, our customers, healthcare professionals, and our employees in this journey because this is what will make us become the &ldquo;Best Fast-Moving Consumer Healthcare (FMCH) Company In &amp; For the World&rdquo;. We strive to act as a force for good by integrating sustainability along our business and employees&rsquo; mission and operate responsibly from both a social and environmental point of view. To achieve this, we need strong talent who will help us shape the future of our Consumer Healthcare business and challenge our industry. At Sanofi Consumer Healthcare, we aspire to create a work environment where people can thrive, grow, and be at their best every day. Our priority is working with integrity to improve the health and well-being of people and communities where we operate, working towards making a positive impact in the world. Our Team: The Global Regulatory Strategy &amp; Science Partner Markets Team is a diverse and inclusive team striving to Build a culture of excellence by: Driving operational effectiveness for regulatory processes Enabling strategic decision making on global regulatory strategy portfolio Bridging regulatory portfolio activities with brand needs Monitoring regulatory performance and budget Ensuring operational excellence and ensuring continuous improvement in Partner Markets (G2) for Science Creating value through a best in class CoE structure, processes and talented resources The CHC Science Center of Excellence (CoE) is an internal resource organization based in India and is set-up to centralize processes and activities to run and support Science Customer functions. The CoE strives to be a partner for strategic and tactical deliveries for CHC Science globally to sustain world-class performance and value.</p><p></p><p><b>
Main </b><b>responsibilities:</b></p><p></p><p><b>
Position Overview:</b></p><p></p><p>
Within the CHC &ndash; Consumer Safety organization, under the direction of the Global Science CoE Lead, the Pharmacovigilance (PV) Agreements Expert will be responsible for management of PV Agreements for CHC products, manages PVA development- planning, execution, maintenance, life cycle management and termination (when applicable) of PVAs and associated deliverables and supports strategy setting, with input as necessary from line management, and supports inspection readiness in relation to PV Agreements.</p><p></p><p><b>
Key </b><b>Responsibilities:</b></p><p>
Develop Pharmacovigilance Agreements (PVA) and support the PVA processes across the CHC organization in liaison with all the stakeholders as follows:</p><ul><li>
Provide guidance to and/or may lead/co-lead projects; develops and manages plans to achieve objectives that relates to business partnerships</li><li>
Consolidate partnerships to promote awareness and understanding of PV Licensing processes and deliverables to ensure effective collaboration with key internal/external interfaces (Regulatory, Business Development, Legal, Contractual Partner, etc).</li><li>
Take informal leadership role during team meetings to facilitate agreements and move toward goals; take responsibility for a portion of the team's deliverables; may lead operational team(s).</li><li>
Support the development of PV Licensing strategies.</li><li>
Actively participate in periodic operational staff meetings to share best practice and foster continuous improvement.</li><li>
In collaboration with the CHC organization functional lines and subject matter experts, drive and implement relevant planning, execution, and governance strategies associated with PV Licensing arrangements enacted in the organization.</li><li>
Support the alignment with CHC Business Development goals as it relates to the overall delivery of quality PV Licensing agreement deliverables.</li><li>
Build strong relationships with relevant customers and stakeholders to drive collaborative partnership with PV Licensing team across the organization when impacting CHC products.</li></ul><p></p><p><b>
About you</b></p><p></p><p><b>
Experience:</b> Experience in consumer healthcare, pharmaceuticals, or related industries, ideally 5+ years in pharmacovigilance or drug safety. Previous experience in driving operational excellence, tracking of KPIs and continuous improvement of processes and performance.</p><p><b><br>
Soft skills:</b> Experience in a CHC product and strategic development environment is essential. Previous experience leading a global organization including management of large multi-country budgets is essential. Significant leadership experience in managing multi-functional teams is required. Ability to work collaboratively in a cross-functional team environment.</p><p><b><br>
Technical skills: </b>Ability to implement strategic efficiency and develop a strategic vision. Ability to evaluate transversal impact on business decision. Ability to provide the strategic vision and leadership to develop and drive strategic CHC sourcing related initiatives with clear objectives through the entire organization. Good knowledge on end-to-end Vendor and contract Management. Experience in building a functional capability from the ground-up highly valued. Proficient in International Regulations, Guidelines, Good Practices pertaining to the pharmaceutical industry standard and practices for medical and Pharmacovigilance.</p><p><b><br>
Education:</b> Higher University level degree (L.L.B, JD, MBA) is mandatory. Basic education in Medical Science stream.</p><p><b><br>
Languages:</b> Excellent knowledge of English language (spoken and written)</p><p></p><p><b>
Pursue progress, discover extraordinary</b></p><p>
Better is out there. Better medications, better outcomes, better science. But progress doesn&rsquo;t happen without people &ndash; people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let&rsquo;s be those people.</p><p>
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.</p><p>
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!</p></div>

Job title: Pharmacovigilance Agreements Expert
Location: Hyderabad
% of travel expected: Travel required as per business need
Job type: Permanent and Full time
About the job
Our Team:
At Sanofi Consumer Healthcare, we have one overarching mission - to work passionately, challenging ourselves and our industry every day, to build a healthier future by helping people, help themselves, bringing “Health in Your Hands”. Our teams are building trusted & loved brands that connect with hundreds of millions of consumers worldwide, enabling better self-care for individuals and communities, while also contributing to a healthier planet. To fulfil this mission, we are embarking our consumers, our customers, healthcare professionals, and our employees in this journey because this is what will make us become the “Best Fast-Moving Consumer Healthcare (FMCH) Company In & For the World”. We strive to act as a force for good by integrating sustainability along our business and employees’ mission and operate responsibly from both a social and environmental point of view. To achieve this, we need strong talent who will help us shape the future of our Consumer Healthcare business and challenge our industry. At Sanofi Consumer Healthcare, we aspire to create a work environment where people can thrive, grow, and be at their best every day. Our priority is working with integrity to improve the health and well-being of people and communities where we operate, working towards making a positive impact in the world. Our Team: The Global Regulatory Strategy & Science Partner Markets Team is a diverse and inclusive team striving to Build a culture of excellence by: Driving operational effectiveness for regulatory processes Enabling strategic decision making on global regulatory strategy portfolio Bridging regulatory portfolio activities with brand needs Monitoring regulatory performance and budget Ensuring operational excellence and ensuring continuous improvement in Partner Markets (G2) for Science Creating value through a best in class CoE structure, processes and talented resources The CHC Science Center of Excellence (CoE) is an internal resource organization based in India and is set-up to centralize processes and activities to run and support Science Customer functions. The CoE strives to be a partner for strategic and tactical deliveries for CHC Science globally to sustain world-class performance and value.
Main responsibilities:
Position Overview:
Within the CHC – Consumer Safety organization, under the direction of the Global Science CoE Lead, the Pharmacovigilance (PV) Agreements Expert will be responsible for management of PV Agreements for CHC products, manages PVA development- planning, execution, maintenance, life cycle management and termination (when applicable) of PVAs and associated deliverables and supports strategy setting, with input as necessary from line management, and supports inspection readiness in relation to PV Agreements.
Key Responsibilities:
Develop Pharmacovigilance Agreements (PVA) and support the PVA processes across the CHC organization in liaison with all the stakeholders as follows:
Provide guidance to and/or may lead/co-lead projects; develops and manages plans to achieve objectives that relates to business partnerships
Consolidate partnerships to promote awareness and understanding of PV Licensing processes and deliverables to ensure effective collaboration with key internal/external interfaces (Regulatory, Business Development, Legal, Contractual Partner, etc).
Take informal leadership role during team meetings to facilitate agreements and move toward goals; take responsibility for a portion of the team's deliverables; may lead operational team(s).
Support the development of PV Licensing strategies.
Actively participate in periodic operational staff meetings to share best practice and foster continuous improvement.
In collaboration with the CHC organization functional lines and subject matter experts, drive and implement relevant planning, execution, and governance strategies associated with PV Licensing arrangements enacted in the organization.
Support the alignment with CHC Business Development goals as it relates to the overall delivery of quality PV Licensing agreement deliverables.
Build strong relationships with relevant customers and stakeholders to drive collaborative partnership with PV Licensing team across the organization when impacting CHC products.
About you
Experience: Experience in consumer healthcare, pharmaceuticals, or related industries, ideally 5+ years in pharmacovigilance or drug safety. Previous experience in driving operational excellence, tracking of KPIs and continuous improvement of processes and performance.
Soft skills: Experience in a CHC product and strategic development environment is essential. Previous experience leading a global organization including management of large multi-country budgets is essential. Significant leadership experience in managing multi-functional teams is required. Ability to work collaboratively in a cross-functional team environment.
Technical skills: Ability to implement strategic efficiency and develop a strategic vision. Ability to evaluate transversal impact on business decision. Ability to provide the strategic vision and leadership to develop and drive strategic CHC sourcing related initiatives with clear objectives through the entire organization. Good knowledge on end-to-end Vendor and contract Management. Experience in building a functional capability from the ground-up highly valued. Proficient in International Regulations, Guidelines, Good Practices pertaining to the pharmaceutical industry standard and practices for medical and Pharmacovigilance.
Education: Higher University level degree (L.L.B, JD, MBA) is mandatory. Basic education in Medical Science stream.
Languages: Excellent knowledge of English language (spoken and written)
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

PVA Expert - Sanofi

PVA Expert

You should have 6+ years in pharmacovigilance, strong global PV knowledge, excellent English, project management skills, and experience with eDMS. A Master's in life sciences is required.

You will coordinate and publish PV regulatory submissions, ensure document quality, train staff on eDMS, manage safety report requests, and liaise with stakeholders for compliance and support.

<div><div><p><b>Job title:</b> Pharmacovigilance Publishing Expert</p></div><div><ul><li><p><b><br>
Location: </b>Hyderabad</p></li></ul></div><div><ul><li><p><b>
% of travel expected: </b>Travel required as per business need</p></li></ul></div><div><ul><li><p><b>
Job type: </b>Permanent and Full time</p></li></ul></div><div><p><b><br>
About the job</b></p></div><p></p><div><p><b><br>
Our Team:</b></p></div><div><p>
At Sanofi Consumer Healthcare, we have one overarching mission - to work passionately, challenging ourselves and our industry every day, to build a healthier future by helping people, help themselves, bringing &ldquo;Health in Your Hands&rdquo;. Our teams are building trusted &amp; loved brands that connect with hundreds of millions of consumers worldwide, enabling better self-care for individuals and communities, while also contributing to a healthier planet. To fulfil this mission, we are embarking our consumers, our customers, healthcare professionals, and our employees in this journey because this is what will make us become the &ldquo;Best Fast-Moving Consumer Healthcare (FMCH) Company In &amp; For the World&rdquo;. We strive to act as a force for good by integrating sustainability along our business and employees&rsquo; mission and operate responsibly from both a social and environmental point of view. To achieve this, we need strong talent who will help us shape the future of our Consumer Healthcare business and challenge our industry. At Sanofi Consumer Healthcare, we aspire to create a work environment where people can thrive, grow, and be at their best every day. Our priority is working with integrity to improve the health and well-being of people and communities where we operate, working towards making a positive impact in the world. Our Team: The Global Regulatory Strategy &amp; Science Partner Markets Team is a diverse and inclusive team striving to Build a culture of excellence by: Driving operational effectiveness for regulatory processes Enabling strategic decision making on global regulatory strategy portfolio Bridging regulatory portfolio activities with brand needs Monitoring regulatory performance and budget Ensuring operational excellence and ensuring continuous improvement in Partner Markets (G2) for Science Creating value through a best in class CoE structure, processes and talented resources The CHC Science Center of Excellence (CoE) is an internal resource organization based in India and is set-up to centralize processes and activities to run and support Science Customer functions. The CoE strives to be a partner for strategic and tactical deliveries for CHC Science globally to sustain world-class performance and value.</p></div><div><p><b><br>
Main responsibilities:</b></p></div><div><p><b><br>
Position Overview:</b></p></div><div><p>
Within the CHC &ndash; Consumer Safety organization, under the direction of the Global Science CoE Lead, the Pharmacovigilance (PV) Publishing Expert will be responsible for distribution of Periodic Safety Reports (PSRs) and will be the process owner for PV Publishing activity in the Company, accountable for distribution of PV reports to countries.</p></div><div><p>
PV Publishing Expert is responsible for providing the strategic vision, planning and oversight on publishing of all CHC PV regulatory documents. This position maintains oversight and responsibility for global publishing vendors.</p></div><div><p><b><br>
Key Responsibilities:</b></p></div><div><ul><li><p>
Responsible for electronic compliant published reports for submission to regulatory agencies and ensure smooth functioning of electronic document management system (eDMS) and publishing systems.</p></li></ul></div><div><ul><li><p>
Responsible for coordination, publishing, and tracking of PV Regulatory submissions. Accountable for submissions packages to be delivered in a timely manner.</p></li></ul></div><div><ul><li><p>
Responsible for delivering on-time published reports in required format and ensure high quality standards of documents by providing necessary quality checks.</p></li></ul></div><div><ul><li><p>
To improve and reinforce standards, procedures and systems in line with changes in the regulatory environment and best industry practices.</p></li></ul></div><div><ul><li><p>
To train, mentor, provide user support to PV personnel/collaborators in the use of eDMS and advanced features of MS (Microsoft) Word.</p></li></ul></div><div><ul><li><p>
Responsible to manage adhoc safety report requests.</p></li></ul></div><div><ul><li><p>
Liaise with RMP (Risk Management Plan) unit and regulatory unit to ensure the required templates and data are uploaded into eDMS and published.</p></li></ul></div><div><ul><li><p>
Provide training and mentoring support to vendor personnel on document management and report publishing activities for PSRs and adhoc safety reports.</p></li></ul></div><div><ul><li><p>
Provide input and feedback on PSR authoring, formatting, and submission readiness at vendor oversight meetings.</p></li></ul></div><div><ul><li><p>
Provide Veeva Vault and publishing support for GPV Regulatory Response Documents, and other adhoc safety reports for submission. Support the review, approval and notification process of reports published in Veeva Vault.</p></li></ul></div><div><ul><li><p>
Ensure successful publishing and submission of Global PSMF in collaboration with QPPV Coordinators.</p></li></ul></div><div><ul><li><p>
Act as subject matter expert for the enhancement or implementation of new eDMS and Publishing tools, quality documents, on template management activities.</p></li></ul></div><div><ul><li><p>
Lead PV special projects related to publishing and document management.</p></li></ul></div><div><ul><li><p>
Liaise with PSR stakeholders to ensure tasks and deliverables meet Regulatory requirements and are in accordance with the QDs.</p></li></ul></div><div><ul><li><p>
This role will be the key contact point for countries and regions for all topics related to PSR distributions.</p></li></ul></div><div><ul><li><p>
This position requires multiple interfaces with partners and customers within and outside of the Company this includes Regulatory, digital and PV.</p></li></ul></div><div><ul><li><p>
Work closely with CHC PSR team members.</p></li></ul></div><div><p><b><br>
About you</b></p></div><div><p><b><br>
Experience: </b>Experience in consumer healthcare, pharmaceuticals, or related industries, ideally 6+ years in pharmacovigilance or drug safety. It requires experience in managing complex issues in a global environment. Strong knowledge of global PV regulations and guidelines (e.g., FDA, EMA, ICH). Proven track record of mentoring a team of PV professionals.</p></div><div><p><b><br>
Soft skills: </b>Stakeholder management, project management, communication and interpersonal skills, strategic thinking and ability to work independently and within a team environment. Strong analytical and problem-solving skills. Ability to work collaboratively in a cross-functional team environment.</p></div><div><p><b><br>
Technical skills:</b> Experience with electronic Document Management Systems and electronic Report Publishing Systems. Advanced working knowledge of MSWord Templates, Adobe Acrobat, and Excel functions. Technical expertise to determine best practice solutions for eDMS system activities and change controls. Develop training material and perform eDMS training for users across the PV Organization. Basic knowledge of PV/safety database and Sales generation software (MARCO). Knowledge of submission-related activities in accordance with Regulatory guidelines. Ability to write/update/contribute to quality documents/job aids/WINs and developing training material to perform training to PV. Ability to manage and lead transversal meetings and small to moderate size groups and take appropriate decisions.</p></div><div><p><b><br>
Education:</b> Master's degree in life sciences or a related field is typically required. Relevant fields include, but are not limited to: Pharmacy, Medicine (Allopathic Medicine only &ndash; no alternative medicine), Biochemistry, Biophysics, Microbiology, Biotechnology.</p></div><div><p><b><br>
Languages:</b> Excellent knowledge of English language (spoken and written)</p></div><div><p><b><br>
Pursue progress, discover extraordinary</b></p></div><div><p>
Better is out there. Better medications, better outcomes, better science. But progress doesn&rsquo;t happen without people &ndash; people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let&rsquo;s be those people.</p></div><div><p>
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.</p></div><div><p><br>
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!</p></div></div><p></p>

Job title: Pharmacovigilance Publishing Expert
Location: Hyderabad
% of travel expected: Travel required as per business need
Job type: Permanent and Full time
About the job
Our Team:
At Sanofi Consumer Healthcare, we have one overarching mission - to work passionately, challenging ourselves and our industry every day, to build a healthier future by helping people, help themselves, bringing “Health in Your Hands”. Our teams are building trusted & loved brands that connect with hundreds of millions of consumers worldwide, enabling better self-care for individuals and communities, while also contributing to a healthier planet. To fulfil this mission, we are embarking our consumers, our customers, healthcare professionals, and our employees in this journey because this is what will make us become the “Best Fast-Moving Consumer Healthcare (FMCH) Company In & For the World”. We strive to act as a force for good by integrating sustainability along our business and employees’ mission and operate responsibly from both a social and environmental point of view. To achieve this, we need strong talent who will help us shape the future of our Consumer Healthcare business and challenge our industry. At Sanofi Consumer Healthcare, we aspire to create a work environment where people can thrive, grow, and be at their best every day. Our priority is working with integrity to improve the health and well-being of people and communities where we operate, working towards making a positive impact in the world. Our Team: The Global Regulatory Strategy & Science Partner Markets Team is a diverse and inclusive team striving to Build a culture of excellence by: Driving operational effectiveness for regulatory processes Enabling strategic decision making on global regulatory strategy portfolio Bridging regulatory portfolio activities with brand needs Monitoring regulatory performance and budget Ensuring operational excellence and ensuring continuous improvement in Partner Markets (G2) for Science Creating value through a best in class CoE structure, processes and talented resources The CHC Science Center of Excellence (CoE) is an internal resource organization based in India and is set-up to centralize processes and activities to run and support Science Customer functions. The CoE strives to be a partner for strategic and tactical deliveries for CHC Science globally to sustain world-class performance and value.
Main responsibilities:
Position Overview:
Within the CHC – Consumer Safety organization, under the direction of the Global Science CoE Lead, the Pharmacovigilance (PV) Publishing Expert will be responsible for distribution of Periodic Safety Reports (PSRs) and will be the process owner for PV Publishing activity in the Company, accountable for distribution of PV reports to countries.
PV Publishing Expert is responsible for providing the strategic vision, planning and oversight on publishing of all CHC PV regulatory documents. This position maintains oversight and responsibility for global publishing vendors.
Key Responsibilities:
Responsible for electronic compliant published reports for submission to regulatory agencies and ensure smooth functioning of electronic document management system (eDMS) and publishing systems.
Responsible for coordination, publishing, and tracking of PV Regulatory submissions. Accountable for submissions packages to be delivered in a timely manner.
Responsible for delivering on-time published reports in required format and ensure high quality standards of documents by providing necessary quality checks.
To improve and reinforce standards, procedures and systems in line with changes in the regulatory environment and best industry practices.
To train, mentor, provide user support to PV personnel/collaborators in the use of eDMS and advanced features of MS (Microsoft) Word.
Responsible to manage adhoc safety report requests.
Liaise with RMP (Risk Management Plan) unit and regulatory unit to ensure the required templates and data are uploaded into eDMS and published.
Provide training and mentoring support to vendor personnel on document management and report publishing activities for PSRs and adhoc safety reports.
Provide input and feedback on PSR authoring, formatting, and submission readiness at vendor oversight meetings.
Provide Veeva Vault and publishing support for GPV Regulatory Response Documents, and other adhoc safety reports for submission. Support the review, approval and notification process of reports published in Veeva Vault.
Ensure successful publishing and submission of Global PSMF in collaboration with QPPV Coordinators.
Act as subject matter expert for the enhancement or implementation of new eDMS and Publishing tools, quality documents, on template management activities.
Lead PV special projects related to publishing and document management.
Liaise with PSR stakeholders to ensure tasks and deliverables meet Regulatory requirements and are in accordance with the QDs.
This role will be the key contact point for countries and regions for all topics related to PSR distributions.
This position requires multiple interfaces with partners and customers within and outside of the Company this includes Regulatory, digital and PV.
Work closely with CHC PSR team members.
About you
Experience: Experience in consumer healthcare, pharmaceuticals, or related industries, ideally 6+ years in pharmacovigilance or drug safety. It requires experience in managing complex issues in a global environment. Strong knowledge of global PV regulations and guidelines (e.g., FDA, EMA, ICH). Proven track record of mentoring a team of PV professionals.
Soft skills: Stakeholder management, project management, communication and interpersonal skills, strategic thinking and ability to work independently and within a team environment. Strong analytical and problem-solving skills. Ability to work collaboratively in a cross-functional team environment.
Technical skills: Experience with electronic Document Management Systems and electronic Report Publishing Systems. Advanced working knowledge of MSWord Templates, Adobe Acrobat, and Excel functions. Technical expertise to determine best practice solutions for eDMS system activities and change controls. Develop training material and perform eDMS training for users across the PV Organization. Basic knowledge of PV/safety database and Sales generation software (MARCO). Knowledge of submission-related activities in accordance with Regulatory guidelines. Ability to write/update/contribute to quality documents/job aids/WINs and developing training material to perform training to PV. Ability to manage and lead transversal meetings and small to moderate size groups and take appropriate decisions.
Education: Master's degree in life sciences or a related field is typically required. Relevant fields include, but are not limited to: Pharmacy, Medicine (Allopathic Medicine only – no alternative medicine), Biochemistry, Biophysics, Microbiology, Biotechnology.
Languages: Excellent knowledge of English language (spoken and written)
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Sanofi

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