Pierre Fabre

Leader regulatory IS , Business administrator - CDI- M/F

Haute Garonne (31) Full time

Who we are ?

We are Pierre Fabre Laboratories, a global leader combining pharmaceutical expertise with dermo-cosmetics to support consumers and patients at every stage of their care journey.
Our portfolio includes several medical franchises and international brands such as Eau Thermale Avène, Ducray, A-Derma, Klorane, René Furterer, and Pierre Fabre Oral Care.
By joining us, you become part of a meaningful company where the human dimension is essential. You become a participant in the "We Care Movement," a movement that values excellence and innovation within passionate teams. Together, we push the boundaries of science to unite health and beauty for the benefit of all, because Every time we care for a single person, we make the whole world better.

Present in 120 countries with a team of over 10,000 employees, we are proud to create a scientific and human impact, today and tomorrow! If caring is at the heart of your values, join Pierre Fabre Laboratories and become a key player in the “We Care Movement".

Your mission

As a Regulatory Systems Leader / Business administrator (Toulouse (31), Boulogne (92) or Castres (81)) within our Worldwide Regulatory Affairs (WRA) organization, you will play a role in shaping the future of our Regulatory Information Systems. On a defined perimeter, you will drive the evolution, reliability, and performance of platforms such as RIM (Registration), Promomats, and other regulatory systems supporting business activities.
Your mission: make our regulatory teams more efficient, more connected, and fully empowered through modern, intuitive, and data‑driven systems.

You will join a collaborative, international, and forward‑thinking environment Business Administration team where innovation, and operational excellence are at the heart of everything we do.

Your role within a pioneering company in full expansion:

Your Key Responsibilities

  • Contributes to defining the strategy for regulatory systems.

    • Ensures alignment with regulatory requirements (in compliance with IS validation rules), business needs, and technological evolutions.
    • Conducts active monitoring of regulatory, technological, and methodological developments that may impact the scope.
  • Leads and oversees the implementation of the defined strategy and ensures its effective deployment across teams and projects.

    • Translates the strategy into operational actions within the relevant technical scopes, defining priorities, milestones, and roadmaps.
    • Coordinates internal and/or external technical and functional teams involved in execution, promoting communication and the sharing of best practices.
  • Provides technical expertise in a complex operational environment to support teams, secure technical decisions, and contribute to the overall performance of the company.

    • Supports teams in analysis, troubleshooting, and technical decision-making; performs complex analyses when required.
    • Contributes to operational risk management related to regulatory systems (obsolescence, end‑of‑life, critical dependencies, etc.).
    • Participates in the onboarding of new team members within the scope of expertise and provides back‑up support on other regulated system areas.
  • Ensures user support by strengthening adoption, understanding, and user satisfaction.

    • Works closely with project teams, business functions (e.g., R&D, Pharmacovigilance, Medical Affairs), DAIS, and any other internal or external stakeholders to ensure overall consistency and measure user satisfaction.

As a Business Administrator

  • User Support and Operational Management

    • Provides first- and second‑level support to users: incident resolution, user guidance, access management, data relevance and accessibility, compliance with administration processes and regulatory requirements.
    • Analyzes technical issues and their operational impact; provides expertise, recommendations, and solutions.
    • In coordination with DAIS and the wider WRA team, manages functional requests and incidents: requirement collection, impact analysis, solution proposal and implementation.
    • Leads or contributes to user training, ensures communication, and strengthens tool and process adoption.
  • Contribution to Releases and System Enhancements

    • Acts as an interface with DAIS and the vendor (e.g., Veeva) on technical topics related to system evolution.
    • Collects business needs, analyzes technical feasibility, and co‑builds solutions aligned with regulatory processes and applicable IS regulations.
    • Drafts technical requirement specifications, integrating business constraints and system capabilities.
    • Manages version upgrades.
    • Performs impact analyses.Defines and executes test plans.
    • Validates production deployment.
    • Ensures regular updates of documentation related to the scope.

This position is compatible with teleworking up to 2 days a week according to company rules.

We offer an attractive remuneration/benefits package: Incentives, profit-sharing, Pierre Fabre shareholding with matching contribution, health and provident insurance, 16 days of holidays (RTT) in addition to 25 days of personal holidays, public transport participation...

    Who you are ?

    Your skills at the service of innovative projects:

    You are a proactive, curious, and solution‑oriented professional with a solid experience in regulatory systems and digital transformation.

    You are comfortable navigating complex environments, engaging with diverse stakeholders, and keeping a global view while managing operational details.

    You’ll be a great match if you have:

    Education Level

    • Master’s degree (Bac +5). Dual background preferred: Pharmacist, Medical Doctor, or Scientist combined with an IT specialization.

    • Or equivalent relevant professional experience.

    Experience

    • At least 5 years of experience in Regulatory Affairs, and at least 5 years of experience in administering regulatory systems (RIM, Promomats, QMS, eCTD tools or similar).
      OR

    • At least 7 years of experience in either Regulatory Affairs or database/system administration, with occasional experience in the other area.

    • Experience in direct or indirect management, including project management, is required.

    Other

    • A strong sense of ownership and the ability to work both independently and collaboratively

    • Excellent communication skills, with the ability to simplify complex topics

    • A mindset oriented toward process optimization and operational excellence

    • A genuine interest in user experience and data integrity

    • A positive, team‑oriented attitude and a desire to make an impact

    • English : Fluent

    At Pierre Fabre Laboratories, we believe that our greatest asset is our people.

    We are committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant or employee based on race, color, religion, creed, national origin or ancestry, sex, sexual orientation, gender identity or expression, age, physical or mental disability, veteran or military status, genetic information, or any other legally recognized protected basis under federal, state, or local law. The information collected by this application is solely to determine suitability for employment, verify identify, and maintain employment statistics on applicants. Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act and certain state or local laws. Please inform the company’s personnel representative if you need assistance completing this application or to otherwise participate in the application process. Thus, we commit to considering all applications equally, without fail.