Stagiaire CMC Regulatory Strategy
About this opportunity
Title:
Stagiaire CMC Regulatory Strategy
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:
Position Summary
Within the Global Regulatory CMC ( Chemistry , manufacturing and controls) team (belonging to Regulatory affairs , part of R&D organization) , the intern will contribute to the optimization, digitalization, and exploitation of regulatory data to support operational excellence, knowledge management, and submission readiness across the Regulatory CMC organization.
The intern will work on practical business projects covering data analytics and visualization, regulatory intelligence, process automation and digital knowledge management.
Key Responsibilities
1-Development of a Regulatory CMC Onboarding SharePoint Platform
Design and implement a dedicated SharePoint site to support onboarding of new Regulatory CMC team members.
Ensure the platform serves as a sustainable knowledge management repository for the team.
Continuously improve the SharePoint site based on user feedback and evolving business needs.
2-Development of Data Analytics and Performance Monitoring Tools
Analyze existing data sources from multiple regulatory systems and databases.
Design and implement data consolidation and visualization solutions using Power BI, advanced Excel, Power Query, Power Automate, and other digital tools.
Identify opportunities to improve data quality, reliability, accessibility, and reporting efficiency.
Explore opportunities to automate and improve the visualization of workload, capacity and resource forecasts.
Support the development of data-driven resource and capacity forecasting tools, using historical workload, project characteristics and activity assumptions to improve resource planning.
3-Regulatory Intelligence, AI and Predictive Analytics
Analyze historical Health Authority questions and regulatory requests across multiple products and regions.
Identify trends, recurring topics, and risk factors associated with regulatory submissions.
Explore the use of AI, machine learning and advanced analytics to identify patterns within regulatory data and knowledge repositories.
Propose predictive tools and methodologies to anticipate potential Health Authority questions during future submissions.
Contribute to the development of a regulatory knowledge repository to facilitate dossier preparation and regulatory strategy planning.
4-Digitalization and Process Improvement Initiatives
Support Regulatory CMC digital transformation projects, including the implementation and optimization of Veeva and other regulatory systems.
Identify automation opportunities to streamline regulatory processes and reduce manual work.
Contribute to continuous improvement initiatives focused on operational efficiency and knowledge management.
Assist the team in adopting new digital tools and best practices
Support good data governance practices, including data quality, consistency, traceability and appropriate use of regulatory information when developing digital solutions.
Candidate Profile
Final-year student pursuing a Master's degree or Engineering degree in Data Science, Business Intelligence, Computer Science, Bioinformatics, Statistics, Digital Transformation, or a related discipline.
Strong interest in data analytics, digital tools, and process optimization.
Advanced knowledge of Excel and Power BI.
Familiarity with Power Automate, VBA, Python, SharePoint development, or related technologies is highly desirable.
Interest in the pharmaceutical industry, regulatory affairs, and life sciences.
Experience or academic exposure to data modelling, data visualization, AI/machine learning or predictive analytics would be an advantage.
Strong analytical and problem-solving skills with the ability to transform complex data into actionable insights.
Excellent communication skills and fluency in English.
Curious, autonomous, proactive, and solution-oriented.
What the Intern Will Gain
Exposure to Regulatory CMC activities within a global pharmaceutical environment.
Hands-on experience in data analytics, business intelligence, knowledge management, and digital transformation.
Opportunity to contribute to strategic initiatives combining regulatory science, digital innovation, and operational excellence.
Experience working with cross-functional stakeholders across Regulatory, Quality, Pharmaceutical Development, and Digital functions.
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
Job details
How this role compares
Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.
We currently track 33 comparable Intern/Fellow/Postdoc Regulatory Affairs roles across 17 biopharma companies.
Salary context
None of this role's 33 tracked peers disclose a salary range yet.
Where these roles are based
Top locations among the 33 comparable roles
+ 9 more countries
Seniority mix
33 of 33 peers have a known seniority level
Therapeutic area mix
1 of 33 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.