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Ipsen Global

Global biopharma focused on specialty care

Vice President, Head of Global Regulatory Operations

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeNo salary listedIn-person

About the Job

Requirements

  • Executive leadership experience within Research and Development in a complex, global biopharmaceutical organization.
  • Proven experience developing and executing global operational strategies that support business growth and regulatory excellence.
  • Demonstrated leadership of large global, geographically dispersed organizations through significant transformation and organizational change.
  • Deep expertise across regulatory submissions, regulatory data, publishing, labelling, regulatory information management, and digital technologies.
  • Strong executive stakeholder management and demonstrated ability to influence senior leaders across Research and Development, Quality, Medical, Commercial, and Digital.
  • Proven experience leading enterprise digital transformation, automation, and artificial-intelligence-enabled initiatives.
  • Experience managing significant operational budgets, strategic vendors, and outsourced partnerships.
  • Demonstrated ability to build inclusive, high-performing organizations and develop future leadership capability.
  • At least 10 years’ experience managing a worldwide Regulatory team.
  • At least 15 years’ experience in the pharmaceutical industry (Research and Development or Pharmacovigilance), 5 years’ experience working in regulatory affairs, and experience managing complex regulatory submissions.
  • Experience in Regulatory Tools Administration, mainly regulatory tracking databases and electronic document management systems.
  • High-level knowledge of information technology tools used for electronic dossier management and publishing, including electronic document management systems, publishing suites, and regulatory tracking systems.
  • Experience implementing data management methodologies and applying data integrity principles.
  • Experience managing regulatory data and Regulatory Data Governance to ensure availability, usability, integrity, and security of high-quality data for the Regulatory Affairs community.
  • Key business analyst skills.
  • Fluency with regulatory review processes.
  • Demonstrable experience leading successful engagement with key regulatory authorities.
  • Proven track record of building and leading teams of skilled regulatory professionals to deliver business results.
  • A bachelor's degree is required.
  • Evidence of management or leadership education, such as an MBA or executive training, is required.
  • Good oral and written communication skills.
  • Fluent English.

Responsibilities

  • Define the strategic direction, operating model, and long-term capability roadmap for Global Regulatory Operations, aligning it with Global Regulatory Affairs, Research and Development strategy, and future business priorities.
  • Lead a global leadership team, building organizational capability, succession plans, and an inclusive, high-performing culture.
  • Represent Regulatory Operations within executive governance forums and influence enterprise decision-making.
  • Own enterprise performance across Regulatory Operations, including regulatory data governance, publishing, submissions, labelling, regulatory systems, and operational delivery.
  • Establish key performance indicators, governance, and performance dashboards to continuously improve quality, compliance, productivity, and customer experience.
  • Ensure inspection readiness and sustainable compliance with evolving global regulatory requirements.
  • Define and deliver the digital transformation strategy for Regulatory Operations, leveraging artificial intelligence, automation, structured content management, and emerging technologies to improve efficiency, scalability, and regulatory effectiveness.
  • Partner with Digital and Information Technology to modernize platforms, strengthen data governance, and develop future-ready regulatory capabilities.
  • Lead global labelling governance to ensure consistency and compliance; implement digital tools for labelling lifecycle management; explore artificial-intelligence-driven solutions for signal detection and automated updates.
  • Provide strategic oversight for major submissions and regulatory milestones.
  • Develop project dashboards and predictive analytics for risk management.
  • Champion agile methodologies for faster delivery under submission excellence.
  • Own and improve the Submission Excellence process and playbook, and support the IND Excellence project.
  • Support inspection readiness for audits of Global Regulatory Affairs.
  • Organize and ensure compliance with global standards and laws applicable to Global Regulatory Affairs, ensuring all systems comply with Global Regulatory Affairs requirements.
  • Establish enterprise governance for Regulatory Operations, ensuring clear decision-making, accountability, risk management, and cross-functional alignment.
  • Sponsor business process harmonization and continuous improvement initiatives across the regulatory value chain.
  • Build strategic partnerships with health authorities, industry associations, technology vendors, and external partners to position the organization at the forefront of Regulatory Operations innovation.
  • Own the Global Regulatory Operations budget, vendor strategy, and investment roadmap.
  • Optimize organizational resources and external partnerships to deliver sustainable operational performance.

Desired Qualifications

  • An advanced degree is preferred.
  • A background in information technology or life sciences is preferred.
  • Fluent French is preferred.

About the Company

Ipsen Global

Global biopharma focused on specialty care

Ipsen is a global biopharmaceutical company that concentrates on specialty care, developing and marketing medicines for oncology, neuroscience, and rare diseases. Its products work by treating specific high-need conditions, ranging from historical diarrhea treatment Smecta to modern targeted therapies in cancer and neurological disorders. The company differentiates itself through a focused portfolio in niche therapeutic areas, growth via strategic acquisitions, and a long-standing family heritage that shaped its international expansion and IPO-driven capital for expansion. Its goal is to address unmet medical needs worldwide by providing effective therapies for patients with serious or rare conditions.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Boulogne-Billancourt, France
Founded
2005

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