Management produit

Informations sur l'entreprise

Nom de l'entreprise : SANOFI
Ville : Bridgewater, NJ 08807

Détails du contrat

Type de contrat : cdi
Type de métier : Regulatory Affairs
Date de publication: 16/06/2022

A propos du recruteur

La vocation de Sanofi est d’accompagner celles et ceux confrontés à des difficultés de santé. Entreprise biopharmaceutique mondiale spécialisée dans la santé humaine, nous prévenons les maladies avec nos vaccins et proposons des traitements innovants. Nous accompagnons tant ceux qui sont atteints de maladies rares, que les millions de personnes souffrant d’une maladie chronique. Sanofi et ses plus de 100 000 collaborateurs dans 100 pays transforment l’innovation scientifique en solutions de santé partout dans le monde. Sanofi, Empowering Life, donner toute sa force à la vie. Chez Sanofi, la diversité et l’inclusion sont au cœur de notre fonctionnement et sont intégrées à nos Valeurs fondamentales. Nous sommes conscients que pour exploiter véritablement la richesse que la diversité nous apporte, nous devons faire preuve d’inclusion et créer un environnement de travail où ces différences peuvent s’épanouir et être développées pour améliorer le quotidien de nos collègues, patients et clients. Nous respectons et valorisons la diversité de nos collaborateurs, leurs parcours et leurs expériences dans un objectif d’égalité des chances pour tous.

Description du poste

At Sanofi CHC, we have one shared purpose - we work passionately, every day, to ‘serve healthier, fuller lives. Our marketing philosophy is driven by this purpose and everything we do is centered around people – our consumers, our customers, healthcare professionals, and our employees – across the world. We are building brands that serve 1bn consumers worldwide, so that they can live healthier, fuller lives. In order to do this better than anybody else, we aspire to become the most consumer-centric Consumer Healthcare company. We want to be market shapers and achieve category leadership in the categories that we play in - delivered through strong global-local partnership. We are a people first business, placing consumers at the heart of everything we do through uncovering and activating deep consumer and shopper insights, for example. As a top 3 global CHC player, we want to raise the bar in terms of our strategic and operational capabilities to enable sustainable, above-market growth. In order to achieve this, we need strong talents that will help us shape the future of CHC while sharing our core values of courage, teamwork, respect, and integrity. We have recently announced an exciting journey to create a fully standalone CHC business (separating the Business Unit from our Pharma company heritage, processes etc.), as we target to create the best FAST MOVING CONSUMER HEALTH company, which will require us to retain, attract and grow the best leaders in our industry. JOB PURPOSE: The Regulatory Promotional & Excellence Lead is a leadership position. He/She will be accountable for fostering the promotional and non-promotional material process and for promoting of best-in-class practices, standards, processes and tools in order to ensure business value, competitive advantage and compliance through expertise and continuous process improvement vision for CHC GBU. Furthermore, He/She will work very closely with Marketing, Commercial to make the bridge between them and Science, Public Affairs, Global Regulatory Affairs, and Digital Media in order to constantly address the business needs, and to exceed business current and future needs. In addition the Regulatory Promotional & Excellence Lead will be a game changing in the promotional area and will be driving complex process improvement projects. Key responsibilities include: Promotional & non-Promotional activities: Building a governance structure on promotional processes and leading its implementation from Global to Local Benchmarking externally to continuously adapt the promotional process to the market needs and also in the perspective of new developments in the digital media area and in Science and Policy in the key countries in alignment and cooperation with the business and all other stakeholders Developing and training of capabilities how to best implement new trends and changes from the digital environment into the promotional materials Optimizing the review process within the DAM tool that vastly accelerates / simplifies the approval process by reducing touch points/ steps / manual interventions, especially for the digital media and ecommerce Training/communication of improved and aligned ways of working and process refinement Being the CHC point of contact in any Sanofi transversal activities related to promotional and non-promotional activities Representing CHC in the Promotional Excellence network within Sanofi and to any relevant committees Validating and consolidating of Regulatory Science and Policy initiatives for the CHC business in terms of promotional materials, including impact assessments, action plans and implementation for new and changing regulations in the company's areas of interest in close cooperation with other key functions Coordinating period reviews and communication of updates for respective global quality documents, providing input and guidance on local quality documents where needed Acting as the Promo Tool Key user for global functions Monitoring pertinent KPls for CHC in terms of Promotional Material Review process lnterfacing with the Claims Leads to foster the Claims validation process in line with the teams' expectations Monitoring and supporting the promotional and non-promotional audit plan (either internai or external) when CHC businesses are involved in interface with the Quality Group Act as CHC regulatory capability lead within the Regulatory academy to ensure regulatory capabilities are considred by the academy Projects Management: Collaborate across Quality & Excellence to define a portfolio of projects/initiatives that aligns with Science quality vision. Characterize risks, propose and drive improvement objectives Ensure timely completion of projects; support resolution of issues or escalation to meet projects objectives/timelines Communication of project progress to all stakeholders. Conduct lessons learned to improve future projects Lead Awareness and Training initiatives using innovative and creative solutions to embark, empower people KEY WORKING RELATIONSHIPS : Strong partnership with CHC Business Interfacing across Science Hub, Quality & Excellence Team, as well as other Global and local teams Transverse leadership role with internal (Global/Regional/Local) and external partners Qualifications & Experience Scientific/health related degree (e.g. MD, PhD, Pharm.D. Bio  engineer) 5-10 years of experience in the pharmaceutical/ consumer healthcare industry, in Regulatory Affairs (global, regional or local), R&D or related area is a nice to have Experience working in project management is a must Experience working in the area of promotional materials PMP certification is required Experience working in the area of digital media desirable Experience working in Consumer Healthcare organization desirable Additional Skills Project / program management Continuous improvement, analytical skills Team collaboration lnterpersonal communication Ability to work in a matrix organization Strong business and customer orientation High standards of integrity Networking Ability to operate successfully in various team capacities and multicultural environment Proficiency in essential regulation guidelines and governance policies and procedures applicable to Scientific Affairs Ability to manage and evaluate complex compliance issues Proficiency in MS Word, Excel, PowerPoint, planning and analytics skills with willingness to go beyond data Ability to deliver training to cross functional groups Language skills Fluent spoken and written English An Additional language is desirable Cultural traits / P2W Behavior Push to go beyond the level we have operated until now:constantly challenge the status quo focusing on the priorities that will deliver the best outcomes and letting go what won’t: be intolerant to mediocracy, believe we can and must do better and aim at higher but never at the expenses of our values and judgment Put the interest of the organization ahead of own of those of his her team :consider both short and long term impact of decisions ; puts collective and global goals above individual or local goals; share resources and capabilities with those with the greatest need and impact; enable decision making at appropriate level Act in the interest of our patients and customers:actively engage with customers to know their current and future needs; brings an external perspective into decisions Take action and don’t wait to be told what to do:take smart and informed best bets with the information at hand and anticipate the consequences of her/his actions; use personal judgement and others’ advice to make bold and impactful decisions which move us forward Role model our 4 values: teamwork, integrity, respect, courage Required Leadership Competencies Build networks to obtain cooperation without relying on authority; strong sensitivity in a multicultural/multinational environment; collaboration skills working across functions and geography, being able to navigate in communication based on your interlocutors Strategic Thinking - ability to evaluate relevant areas of operation, formulate objectives and set priorities in a contextually relevant way, and develop plans consistent with long-term organizational interests Business Acumen – Ability to effectively use specific indicators to fully understand and improve business results Judgement- The ability to draw logical conclusions based on acquired information and analytical rigor in problem-solving, the ability to make effective decisions even when information is ambiguous or incomplete Interpersonal relationships - treating others with courtesy, sensitivity, and respect. Personal Leadership - Personal leadership translates into courage, choice, and commitment through the pursuit of excellence, trust, and accountability.  Ability to put patient, stakeholder, and organizational interests above personal interests Drive -Takes the lead and initiates activities with a high degree of passion and commitment as well as the drive, desire and need to achieve challenging goals, to improve performance or to meet personal standards of excellence Learning Agility – Ability to navigate first time/unfamiliar situations effectively by extrapolating from other areas of expertise and knowledge. Ability to continuously improve and develop self As a healthcare company and a vaccine manufacturer, Sanofi has an important responsibility to protect individual and public health. All US based roles require individuals to be fully vaccinated against COVID-19 as part of your job responsibilities. According to the CDC, an individual is considered to be “fully vaccinated” fourteen (14) days after receiving (a) the second dose of the Moderna or Pfizer vaccine, or (b) the single dose of the J&J vaccine. Fully vaccinated, for new Sanofi employees, is to be fully vaccinated 14 DAYS PRIOR TO START DATE. Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. #GD-SA#LI-SA

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