Head of Global Regulatory Operations

Posted 4 Days Ago
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2 Locations
In-Office
Expert/Leader
Healthtech • Manufacturing
The Role
Lead Global Regulatory Operations to define strategy, governance and capabilities for regulatory data, submissions, labelling and digital platforms. Drive transformation via AI, automation and data governance; ensure inspection readiness, deliver submission excellence, manage budgets, vendors and cross-functional stakeholder relationships while building a high-performing global team.
Summary Generated by Built In

Title:

Head of Global Regulatory Operations

Company:

Ipsen Innovation (SAS)


 

About Ipsen:

Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation.

 Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!

For more information, visit us at https://www.ipsen.com/ and follow our latest news on LinkedIn and Instagram.

Job Description:

The Head of Global Regulatory Operations provides enterprise leadership for Regulatory Operations across Global Regulatory Affairs (GRA), defining the long-term vision, operating model and capabilities required to enable Ipsen's global regulatory strategy. The role is accountable for ensuring world-class regulatory operations through excellence in regulatory data, digital platforms, submissions, labelling governance and operational execution.

As a member of the Global Regulatory Affairs Leadership Team, the VP partners across R&D, Quality, Medical, IT and Commercial functions to drive enterprise transformation, accelerate regulatory delivery and strengthen Ipsen's competitive advantage through innovation, digitalization and operational excellence.

The role is accountable for:

  • Defining and executing the Global Regulatory Operations strategy aligned with Ipsen's corporate and R&D objectives.
  • Leading the transformation of Regulatory Operations through digital innovation, AI, automation and data-driven decision making.
  • Building a high-performing global organization that delivers operational excellence, inspection readiness and sustainable business performance.
  • Providing enterprise governance for regulatory systems, regulatory data, submission management and global labelling.
  • Driving a culture of collaboration, accountability, innovation and continuous improvement.

Main Responsibilities & Technical Competencies

Enterprise Leadership & Strategy:

  • Define the strategic direction, operating model and long-term capability roadmap for Global Regulatory Operations, ensuring alignment with Global Regulatory Affairs, R&D 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.

Operational Excellence

  • Own enterprise performance across Regulatory Operations including regulatory data governance, publishing, submissions, labelling, regulatory systems and operational delivery.
  • Establish KPIs, governance and performance dashboards to continuously improve quality, compliance, productivity and customer experience.
  • Ensure inspection readiness and sustainable compliance with evolving global regulatory requirements.

Digital Transformation

  • Define and deliver the digital transformation strategy for Regulatory Operations, leveraging AI, automation, structured content management and emerging technologies to improve efficiency, scalability and regulatory effectiveness.
  • Partner with Digital & IT to modernize platforms, strengthen data governance and develop future-ready regulatory capabilities.

Labelling (CCDS, USPI and SmPC)

  • Lead global labelling governance ensuring consistency and compliance; implement digital tools for labelling lifecycle management; explore AI-driven solutions for signal detection and automated updates.

Regulatory Project Management

  • 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 Submission Excellence process & playbook, support IND Excellence project

Compliance

  • Support inspection readiness for audits of Global Regulatory Affairs
  • Organizes and ensures compliance to global standards & laws applicable to Global Regulatory Affairs, ensuring all systems are in compliance with GRA requirements.

Enterprise Governance

  • 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.

External Leadership

  • Build strategic partnerships with Health Authorities, industry associations, technology vendors and external partners to position Ipsen at the forefront of Regulatory Operations innovation.

Financial & Resource Management

  • Own the Global Regulatory Operations budget, vendor strategy and investment roadmap.
  • Optimize organizational resources and external partnerships to deliver sustainable operational performance.

Knowledge & Experience

Knowledge & Experience (essential):

  • Executive leadership experience within Research & 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 organisations through significant transformation and organisational change.
  • Deep expertise across regulatory submissions, regulatory data, publishing, labelling, regulatory information management and digital technologies.
  • Strong executive stakeholder management with demonstrated ability to influence senior leaders across R&D, Quality, Medical, Commercial and Digital.
  • Proven experience leading enterprise digital transformation, automation and AI-enabled initiatives.
  • Experience managing significant operational budgets, strategic vendors and outsourced partnerships.
  • Demonstrated ability to build inclusive, high-performing organisations and develop future leadership capability.

Knowledge & Experience (preferred):

  • At least 10 years’ experience managing a worldwide Regulatory team
  • At least 15 years’ experience in Pharmaceutical Industry (R&D or Pharmacovigilance), 5 years’ experience working in regulatory affairs, experience in managing complex regulatory submissions
  • Experience in Regulatory Tools Administration (mainly regulatory tracking database and EDMS)
  • High level knowledge in IT tools used for electronic dossier management and publishing: electronic document management systems, publishing suites, regulatory tracking systems
  • Experience in the Data management methodology implementation and Data integrity principles
  • Experience in the management of regulatory data and the Regulatory Data Governance to ensure availability, usability, integrity and security of high-quality data for RA community
  • Key business analyst skills
  • Fluent with the review regulatory processes
  • Demonstrable experience of leading successful engagement with key regulatory authorities
  • Proven track record in building and leading teams of skilled regulatory professionals to deliver business

Education / Certifications (essential):

  • Bachelor’s degree
  • Evidence of management/leadership education (MBA or executive training)

Education / Certifications (preferred):

  • Advanced degree preferred
  • Background in IT technologies or life sciences preferred

Language(s) (essential):

  • Good oral and written communication skills
  • Fluent English

Language(s) (preferred):

  • Fluent French (preferred)

Nous nous engageons à créer un lieu de travail où chacun se sent écouté, valorisé et soutenu, où nous incarnons « The Real Us*». La valeur que nous accordons aux différentes perspectives et expériences motive notre engagement en faveur de l'inclusion et de l'égalité des chances. Lorsque nous intégrons des modes de pensée diversifiés, nous prenons des décisions plus réfléchies et découvrons des solutions plus innovantes. Ensemble, nous nous efforçons de mieux comprendre les communautés que nous servons. Cela signifie que nous voulons également vous aider à donner le meilleur de vous-même lorsque vous postulez à un poste chez nous. Si vous avez besoin d'aménagements ou d'aide pendant le processus de candidature, veuillez en informer l'équipe de recrutement. Ces informations seront traitées avec soin et n'auront aucune incidence sur le résultat de votre candidature. *Soyons nous-même

Skills Required

  • Executive leadership experience within R&D in a global biopharmaceutical organization
  • Proven experience developing and executing global operational strategies supporting regulatory excellence
  • Demonstrated leadership of large, geographically dispersed organisations through transformation and change
  • Deep expertise across regulatory submissions, regulatory data, publishing, labelling and regulatory information management
  • Strong executive stakeholder management and ability to influence senior leaders across R&D, Quality, Medical, Commercial and Digital
  • Proven experience leading enterprise digital transformation, automation and AI-enabled initiatives
  • Experience managing significant operational budgets, strategic vendors and outsourced partnerships
  • Demonstrated ability to build inclusive, high-performing organisations and develop future leadership capability
  • Bachelor's degree
  • Evidence of management/leadership education (MBA or executive training)
  • Good oral and written communication skills; Fluent English
  • At least 10 years' experience managing a worldwide Regulatory team
  • At least 15 years' experience in the Pharmaceutical Industry; 5 years' experience working in regulatory affairs
  • Experience in Regulatory Tools Administration (regulatory tracking database and EDMS)
  • Knowledge of electronic dossier management, publishing suites and regulatory tracking systems
  • Experience implementing data management methodology and data integrity principles; Regulatory Data Governance experience
  • Key business analyst skills and familiarity with predictive analytics and dashboards
  • Advanced degree (preferred)
  • Background in IT technologies or life sciences (preferred)
  • Fluent French

Ipsen Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Ipsen and has not been reviewed or approved by Ipsen.

  • Healthcare Strength Health coverage is described as comprehensive, with broad medical, dental, and vision offerings. Company materials emphasize a wide-ranging package that supports overall wellbeing.
  • Retirement Support Retirement programs are highlighted with a competitive 401(k) match and access to an employee stock purchase plan. These elements are frequently cited as strengths in the package.
  • Parental & Family Support Family support includes paid parental leave and company-provided backup child and elder care. These programs complement core benefits and add practical day-to-day value.

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The Company
HQ: Boulogne-Billancourt
5,848 Employees

What We Do

Ipsen is a French leading global mid-size biopharmaceutical company headquartered in Paris, France focusing its efforts where unmet medical needs are greatest. Ipsen develops and commercializes innovative medicines in three key therapeutic areas - Oncology, Rare Disease and Neuroscience. We have over 5000 employees worldwide and our medicines are registered in more than 100 countries, with direct commercial presence in over 30 countries. Ipsen has 4 global R&D hubs and 3 pharmaceutical development centers around the world

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