Regulatory Affairs Expert

il y a 2 jours


Paris, France Qonto Temps plein

**Our mission**? Making day-to-day banking easier for SMEs and freelancers thanks to an online business account that's combined with invoicing, bookkeeping and spend management tools. Thanks to its innovative product, highly reactive 24/7 customer support and clear pricing, Qonto has become the leader in its market.

**Our journey**: Founded by Alexandre and Steve in July 2017, Qonto has rapidly gained trust, serving over 500,000 customers. Thanks to our wonderful team of 1,600+ Qontoers, we also made it to the LinkedIn Top Companies French ranking

**Our values**:
**Customer focus |** Prioritize customers in everything you do

**Ownership |** Own your part, get things done

**Teamwork |** Make (team)work easy

**Mastery |** Continuously raise the bar

**Integrity |** Always do what’s right, and respect people

**Our beliefs**: At Qonto, we're committed to fostering a welcoming environment where everyone can thrive. We prioritize evaluating applicants based solely on skills and potential, ensuring diversity with 50% international team members, 44% women, and 20% parents. Join us in building a workplace that celebrates diversity and individuality.

Discover the steps we took to create a discrimination-free hiring process.

Join Qonto as a **Regulatory Affairs Expert** and play a **pivotal role in managing our relationships with Supervisory Authorities and providing regulatory advice.** Your expertise will ensure Qonto's compliance and support our expansion into new markets, working closely with your manager Alexandre, to achieve our strategic goals.

‍‍ **As a Regulatory Affairs Expert at Qonto, you will**:

- **Manage the relationship with Qonto’s supervisory authorities**, such as the ACPR or the Banque de France, you will ensure that Qonto provides accurate, precise, and consistent information to our Supervisors.
- **Coordinate internal responses to regulatory inquiries**, liaising with other Qonto departments such as Risk & Compliance, Finance, Operations, and many others.
- **Actively participate in projects led by Qonto’s Strategy, Product, & Growth** to advise on the prudential requirements, and act as a solution-oriented stakeholder.
- **Be ready to tackle new internal projects** in line with Qonto’s overall growth and strategic priorities.

**What you can expect**:

- Join a dynamic Regulatory team of 10 professionals within the Risk & Compliance department.
- **Enter a fast-paced Fintech environment** at Qonto, where innovation and agility drive our success.
- Become one of the **key experts in Qonto's second line of defense** to support teams on international projects involving supervisory authorities, as the role evolves.

**Your Future Manager**

Your manager will be Alexandre, our Head of Regulatory.
- **His path?** Has a variety of experience in banking regulation, compliance, and engagement with public authorities.
- **What he can bring to the team?** Alexandre created the Regulatory team at Qonto from scratch. His scope not only includes France but also our international markets (Italy, Spain, and Germany). He is our DPO and the one in direct connection with Qonto’s supervisors (ACPR, CNIL, branch supervisors)

**About You**:

- **At least 4 years of experience in a licensed institution or a supervisory authority**, working in direct contact with supervising authorities.
- Ability to **adapt and simplify complex juridical information** for diverse audiences.
- **Strong communication skills in both French and English**:

- **Attention to detail** and at ease with communicating regulatory constraints & risks, including to senior management.
- Good mastery of the regulatory topics related to regulatory analysis (CRR2/CRR3)

**Perks**

A tailor-made and dynamic career track. An inclusive work environment. And so much more to help you succeed.
- Offices in Paris, Berlin, Milan, Barcelona, and Belgrade;
- Competitive salary package;
- A meal voucher;
- Public transportation reimbursement (part or global);
- A great health insurance (depending on the country);
- Employee well-being initiatives: access to Moka Care to take care of your mental health and great offers for sports and wellness activities;
- A progressive disability and parenthood policy (1 in 6 of Qonto employees is a parent) and childcare benefits with selected partners;
- Monthly team events.

**Our hiring process**:

- Interviews with your Talent Acquisition Manager and future managers
- A remote exercise to demonstrate your skills and give you a taste of what working at Qonto could be like

We will send you an **interview guide** so you can best prepare yourself.

On average, our process lasts **20 working days** and offers usually follow within **48 hours**

To learn more about us:
Qonto's Blog | Les Échos I L'Usine Digitale | Courrier Cadres


  • Regulatory Affairs Assistant

    il y a 2 semaines


    Paris, Île-de-France Scienta Temps plein

    We are partnered with a Global Consumer Health Business, looking for a Regulatory Affairs Assistant for their International Regulatory Affairs Team.ResponsibilitiesPrepare and compile documentation for product registrations, renewals, and variations.Coordinate submissions with local authorities and track progress.Manage administrative tasks such as...


  • Paris, France KGR Temps plein

    We are recruiting a Regulatory Affairs Specialistfor a global not-for-profit organization in Paris. Your tasks: - Coordinate with the team to plan, organize and submit regulatory submissions to national Health Authorities - Address regulatory queries from notifying bodies, Health Authorities and distributors and maintain regulatory approvals - Ensure that...

  • Regulatory Affairs Officer

    il y a 2 semaines


    Paris, France Excelya Temps plein

    **About the Job** Join Excelya as a **Regulatory Affairs Officer** specializing in **Medical Devices**, where **Audacity, Care, and Energy** define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. This role is an exciting opportunity to...


  • Paris, France Bolt Technology Temps plein

    We are looking for a **Vice President of Global Regulatory Affairs & Public Policy** to join Bolt's team and lead all of our regulatory and policy efforts. You will be in charge of a team of over 40 regulatory and policy professionals, guiding them and the company on all regulatory and policy matters, and liaising closely with senior management. In this...


  • Paris 1er, France BIORASI LLC Temps plein

    **We are Growing**! Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization, and we are unlike any CRO you’ve ever heard of. Biorasi is looking for top...

  • Regulatory Affairs Specialist

    il y a 2 semaines


    Paris, France Anderson RH Temps plein

    Excellent knowledge of EU regulatory medical device guidelines - Previous global experience within the pharmaceutical/medical device industry within Regulatory Affairs - Excellent written and verbal communication skills in English To strengthen our RA team based in Paris, we are seeking a Global Regulatory Affairs Specialist. This role is full time,...


  • Paris, France JM Huber Corporation Temps plein

    **Summary**: **Key Responsibilities**: - Develop, implement, and manage regulatory strategies to ensure compliance with applicable regulations and standards. - Monitor changes in relevant regulatory environments, interpret new and existing regulations, and communicate potential impacts to key stakeholders. - Provide expert guidance on regulatory matters...


  • Paris, France Nanobiotix Temps plein

    Nanobiotix is happy to welcome a CMC manager, regulatory affairs to provide valuable support to our mission to advance groundbreaking nanomedicine solutions. At the forefront of pioneering nanomedicine approaches that could redefine cancer treatment, our team at Nanobiotix is dedicated to creating innovative solutions to impact countless lives across the...

  • Biocidal Team Leader

    il y a 2 semaines


    Paris, France Staphyt Group Temps plein

    At Staphyt, our Regulatory Affairs Division helps clients navigate complex regulatory environments and successfully bring their chemical or biological substances and products to market. We support projects across Plant Protection & Nutrition, Biocides and REACh sectors. Skills, experience and geographical coverage are three essential assets of our team to...

  • Regulatory Affairs Manager

    il y a 2 semaines


    Paris, France elemed Temps plein

    OverviewTitle: Senior Consultant – Device Regulatory Documentation & ComplianceLocation: Paris (3 days onsite - 2 WFH)The CompanyWe believe great work happens when brilliant minds come together with a shared purpose. This biopharma company is known for its dedication to employee happiness, its collaborative environment, and its passion for bringing...