Head of Regulated Applications
作为新的监管应用程序负责人，你有独特的机会建立一个高性能组织，通过安全，合规和可扩展的应用服务实现数字化转型。承担对关键业务监管应用的总体责任。作为监管应用公司负责人，你将直接报告给全球 IT 负责人副总裁，并成为全球 IT 领导团队成员。你将建立和领导监管应用功能，并为支持研发和其他受管制业务领域的重要 GxP 应用程序战略，治理和生命周期管理负全部责任。在这个角色中，你将建立，领导和发展受监管的应用程序团队，培养合作，问责制和持续改进文化。你将定义并执行应用战略和路线图，确保业务优先事项，技术创新和法规要求之间的协调，并且将领导全球转型倡议，包括维瓦等企业平台，以确保从实施到可持续运营的成功过渡。你将拥有受监管应用组合，确保有效治理，合规性，验证，网络安全，风险管理和检查准备。你将与研究和开发，质量，企业架构，网络安全及外部供应商的高级利益相关者密切合作，不断提高业务能力和用户体验，同时监督供应商管理，外包服务，软件许可，服务性能和运营预算。经验丰富的应用专业人员具有经验证实领导经验。你在计算机科学，生命科学，工程，信息技术，商业或其他相关学科中获得有关大学学位，并带来药品，生物技术或医疗器械行业内领先应用管理经验证实的经验。你负责监管 GxP 应用程序，理想情况下可以与 Veeva 等平台或类似的 GxP 监管企业解决方案有经验。此外，你对应用程序生命周期管理，IT 治理，验证，合规，供应商管理，预算和服务提供具有强大的理解。个人来说，你具有积极主动性和决心推动创新的感觉。你在解决问题方面采取积极的方法，并将公司的支持率提高。
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As the new Head of Regulated Applications, you have a unique opportunity to build a high-performing organization that enables digital transformation through secure, compliant and scalable application services.
Assume overall responsibility for business-critical regulated applications
As Head of Regulated Applications, you will report directly to the VP, Head of Global IT and become a member of the Global IT Leadership Team. You will establish and lead the Regulated Applications function with end-to-end responsibility for the strategy, governance and lifecycle management of business-critical GxP applications supporting R&D and other regulated business areas. In this role, you will build, lead and develop the Regulated Applications team, fostering a culture of collaboration, accountability and continuous improvement. You will define and execute the application strategy and roadmap, ensuring alignment between business priorities, technology innovation and regulatory requirements, and you will lead global transformation initiatives, including enterprise platforms such as Veeva, ensuring successful transition from implementation into sustainable operations. You will own the regulated application portfolio, ensuring effective governance, compliance, validation, cybersecurity, risk management and inspection readiness. You will partner closely with senior stakeholders across R&D, Quality, Enterprise Architecture, Cyber Security and external vendors to continuously improve business capabilities and user experience, while also overseeing vendor management, outsourced services, software licensing, service performance and operational budgets.
Experienced Application Professional with proven leadership experience
You hold a relevant university degree within Computer Science, Life Science, Engineering, Information Technology, Business, or a related discipline, and bring proven experience leading application management within the pharmaceutical, biotechnology or medical device industry. You have responsibility for regulated GxP applications and ideally bring experience with platforms such as Veeva or similar GxP regulated enterprise solutions. Furthermore, you possess a strong understanding of application lifecycle management, IT governance, validation, compliance, vendor management, budgeting, and service delivery.
Personally, you are characterized by a keen sense of initiative and determination to drive innovation. Your proactive approach to problem-solving, coupled with exceptional communication skills, facilitates effective interactions with stakeholders at all levels and is skilled at translating complex technical topics into clear business value. Your self-driven nature manifests in a strong sense of urgency and determination to propel projects forward.
As a leader, you develop high-performing teams through empowerment, coaching, and clear direction. You are comfortable with hands-on leadership and operating across both business and technology domains. You foster a culture of accountability, innovation, and continuous improvement, and you are equally comfortable guiding teams through operational challenges and organizational change. You combine strategic vision with operational excellence, demonstrating the ability to translate complex business challenges into scalable digital solutions.
Play a pivotal role in a unique and exciting international growth journey
This is your opportunity to join Pharmacosmos at a time of strong ambition and continued investment and become part of a competent Global IT organization that supports the business in seizing opportunities to benefit more patients globally and address unmet medical needs. The recruitment process is carried out by Venaris Executive Search. The recruitment process is carried out by Venaris Executive Search (). For more information regarding the position, please reach out to Senior Executive Search Consultant, Lars Nordlund Bidstrup on +45 3123 3018. All requests will be handled confidentially. If this position is for you, do not hesitate to apply by uploading your CV - it is not necessary to include a cover letter.
About Pharmacosmos
Pharmacosmos A/S is a global leader in carbohydrate chemistry and innovative treatments for iron deficiency and iron deficiency anaemia. Building on our foundational expertise in carbohydrate chemistry and cell cycle biology, we develop innovative treatments for unmet patient needs, with a focus on iron metabolism and blood-related disorders. Founded in 1965 and headquartered in Denmark, our team is made up of more than 650 specialists across the UK, Ireland, the Nordics, Germany, Canada, and the USA. Learn more about Pharmacosmos at .
Originally posted on Himalayas