跳至主要内容
两名身穿白色实验室外套的女性一起看着电脑屏幕

Africa Partner Markets Regulatory Lead - French Speaker

Mégrine, 突尼斯
开罗, 埃及
Permanent 发布日期 Aug. 19, 2024
立即申请

JOB PURPOSE

The Africa Partner Markets Regulatory Lead will:

  • manage and coordinate the regulatory activities in the G2 Norwest Africa markets.
  • ensure the regulatory compliance and data needs including regulatory quality compliance, regulatory database updates and maintenance, etc.  
  • support the portfolio approach for Science value creation ensuring clear priorities are defined and delivered within the areas of responsibilities.
  • ensure the vision for the country activities are delivered within timelines agreed.
  • Lead the oversight on the G2 Norwest Africa Partners.

KEY RESULTS/ACCOUNTABILITIES

Examples of Regulatory Activities:

  • Ensuring compliance of the existing CHC portfolio, effective and timely approval of all marketing authorizations, maintenance, provide appropriate input on the development of new products and shape the regulatory environment in the markets in scope through close collaboration and interaction with the Partner/s.
  • Ensure advice and input is provided to local business strategies with regards to regulatory feasibility, requirements, and timelines.
  • Ensure high quality submissions within timelines agreed with Science counterparts, business and/or health authorities
  • Foster an environment/culture of learning and sharing of best practice within the team.
  • Optimize on cross-functional support within the organization, ensuring effective communication with Science counterparts, key stakeholders like marketing and business teams to deliver on all priorities.
  • Foster a close and collaborative relationship with the Partners with regular updates on submissions and regulatory strategic plans.

Examples of regulatory compliance activities:

  • Ensure product packaging and associated information are updated, timely implemented and maintained in accordance with the current product licenses.
  • Ensure that Marketing Authorizations are updated in line with Company Core Safety Information according to Corporate requirements
  • Ensure compliance and training to all mandatory SOPs is completed
  • Ensure quality and compliance of local regulatory activities in line with corporate policies, national regulations. Ensure maintenance of regulatory databases.
  • Work closely with the Partner to actively follow the development and emergence of new regulatory requirements and assess their impact on the existing products and in development.
  • Review and approve promotional and non-promotional materials ensuring their compliance with local regulations, code of conduct and internal guidelines. Coordinate review with the responsible functions in the country. Ensures consistency and conformity to the various published guidelines – Opella., Legislation, and Industry code, as applicable.
  • Liaison with local manufacturing facility & the partner in connection with all aspects that affect the dossier held by the relevant Regulatory Authorities. 

Examples of Health Authority Interactions activities:

  • Support the Partner on any company and local regulatory authorities’ inspections.
  • Build good relationship (directly or via the Partner), making Opella. a recognized partner with the agencies
  • Develop and facilitate relations with key regulatory authorities and decision-makers at a market level when relevant; discuss and challenge issues and negotiate solutions in the best interests of the company, in partnership with the Partner.

Examples of Regulatory Environment influence activities

  • In markets where applicable, support the Partner in shaping the Regulatory environment through active contribution in Zone industry associations and in collaboration with Public & Government Affairs

Examples of Portfolio Management activities:

  • Support the management of the local maintenance activities and ensure compliance of the marketed product portfolio in the countries in scope.
  • Support development of the Local Regulatory strategies for geographical extensions
  • Manage the preparation of local dossiers for the products under development and territory extensions in collaboration with the Partner
  • Support development of local strategies and preparation of local OTC switches
  • Ensure that best efforts are provided to get timely approvals of dossiers and all risk mitigation plans are in place to avoid any undue risk to business, in partnership with relevant stakeholders.

Examples of Drug Development activities:

  • Give Input to Global teams for drug development with regards to local needs (labelling, clinical trials), with support from the Partner, when relevant

Examples Risk Management activities:

  • Co-ordinate the local health authority approval and implementation of risk management plans and educational material, in strong collaboration with the Partner
  • Ensure public availability of current approved product information for risk minimization (SmPC, educational material, PIL, compendia) is done when relevant

Examples of Portfolio Optimization activities:

  • Provide RA input to product portfolio optimization and product pruning and give RA input to global product portfolio optimization strategies and constantly and proactively engage with Has through the Partner when relevant

Examples of Regulatory Database Management activities:

  • Lead the compliance of the regulatory registration database.
  • Ensure regular tracking and closure of submissions in global databases.

KEY WORKING RELATIONSHIPS

Science stakeholders, Business, marketing, external partners

SKILLS, EXPERIENCE & KNOWLEDGE REQUIREMENTS

Education

  • Degree in Pharmacy or Science Degree or relevant Academic qualification is desirable.
  • Current and valid certification in line with the local regulations, an advantage.

Required knowledge and/or experience

  • Extensive experience in Regulatory Affairs, with a minimum of 5 years’ experience
  • Working experience in the French Africa Zone particularly in a North African area.
  • Good understanding of the consumer healthcare and pharmaceutical industry, drug development environment, and R&D processes and objectives
  • Knowledge of the local Consumer Health environment (regulatory, Zoneal Industry Associations, Public & Government affairs).
  • Demonstrated success in partnering and influencing across a matrix environment with exceptional executive communication skills

Language skills

  • Fluent spoken and written French and English (mandatory)
  • An Additional language is desirable

Cultural traits

  • 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

  • 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 economic, financial, market, stakeholder, and industry-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
  • Team Leadership – Ability to build cohesive, high-performance teams that take accountability and achieve required results
  • Interpersonal relationships - treating others with courtesy, sensitivity, and respect.
  • Change Leadership - The ability to demonstrate support and drive for innovation and organizational transformation
  • 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.

追寻 发展探索 菲凡

进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。

在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。

观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!

立即申请
  • 您还没有查看任何职位。

  • 您还没有保存任何职位。

白板上的男人指着演示文稿并看着同事

查看所有职

我们的产品设计师负责帮助人们提高免疫力,物流专家负责将药物送到需要的人手中,而数据分析师则借助先进的技术改善人们的生活。在医疗健康领域,每一次进步都离不开所有人的努力。您可以自由选择自己的职业发展道路。Gig零工项目将帮助您尝试更多岗位,个性化指导将为您挖掘自己从未被发现的优势。加入我们,开启菲凡的职业发展之路。您到底可以走多远?让我们拭目以待!

体验可能性

  • Ama

    Ama puts her project management techniques and ServiceNow knowledge to use to help advance Sanofi’s Digital Data operating model. Learn how our team connects data and AI to do what’s never been done before.

    了解更多
  • Cambridge Crossing

    We're bringing together 2,500 people from across our organization — R&D, Medical, Commercial and Global colleagues all working to realize the power of collaboration.

    了解更多
  • Innovation in Action

    Our flexible lab of the future will transform how we conduct research, while our innovation center will be fully integrated with existing R&D locations.

    了解更多
  • Sanofi’s AI Centre of Excellence in Toronto

    The Centre is focused on using leading technologies to develop world-class data and artificial intelligence (AI) products to create value for the health sector.

    了解更多
  • Sanofi Canada's Philanthropic Efforts

    By chasing the miracles of science to improve people’s lives, we surprise ourselves with what we can achieve. Our team is humbled by the impact our efforts make.

    了解更多
  • Sustainable and Green

    Our new facility was built to minimize the environmental impact — helping protect our planet and people. Using resources efficiently, we're providing greener, healthier workspaces.

    了解更多
  • 您保存的职位

    了解更多
  • 我们的办公地点

    我们的员工遍布60多个国家/地区。他们勠力同心,携手共创医疗健康领域的美好未来。无论您在哪里工作,我们的专家都会指导您推动职业发展,您也将能够运用先进的科学技术,取得意义非凡的重大突破。

    了解更多
  • 勇敢追梦,奔赴美好未来

    想要改变自己的生活,乃至改变全球数百万人的生活,该怎么做?加入我们,开启职业新篇章,然后在我们的保驾护航中展翅高飞,并向优秀的人求教,为这份事业做出切实的贡献。

    了解更多
  • 您和我们相互依存,共同成长

    我们精心打造薪酬体系,为您的身心健康、财务健康与社交健康提供全面保障。我们有着海纳百川的包容性团队文化,无论您在哪个岗位,都能展翅高飞。

    了解更多
  • 心怀梦想,成就一番事业

    我们希望您以饱满的热情投入到自己的工作岗位中,给全球数百万人带来美好生活。您的职业发展道路由您自己来掌控。您只管制定目标,我们会提供充足的培训机会和支持,让您得偿所愿。

    了解更多
  • 我们的人与文化

    我们是首个建立多元化、公平性和包容性(DE&I)委员会的制药企业。我们还建立了“菲常联盟”,为每位员工提供发声的平台。您的声音是我们建设未来道路的重要基石。

    了解更多
  • 我们的故事

    我们关注每一个员工的声音。因为,我们的未来取决于所有员工的付出与努力。正因为他们的助力,我们才能追求远大的理想。

    了解更多
  • 为什么选择我们?

    我们为您提供各种工具、支持和培训机会,帮助您实现自己的目标。我们也希望您充分发挥潜力,帮助我们实现目标:将新药研发到临床治疗的时间减半。

    了解更多