Job ID R-507484 Date posted January 12, 2025

Be part of something bigger at BD. Here, you’ll help us maintain our high standards from a regulatory perspective at all levels, with a keen focus on submissions. It requires acute attention to detail, excellent communication skills and a passion to keep learning and updating your knowledge, which we’ll help you do with regular learning opportunities. Here, you’ll use your in-depth knowledge of FDA, Canadian and ISO/MDD regulations and requirements surrounding medical devices to ultimately achieve a singular goal: advancing the world of health™. At BD, you can make a true difference of one.

  • Job Type:
    Full-Time
  • Job Level:
    Entry to Senior
  • Travel:
    Varies
  • Salary:
    Competitive
  • Glassdoor Reviews and Company Rating

Responsibilities

Job Description Summary

Au sein du site du Pont-de-Claix (38)/Eybens (38), vous intégrerez le service Affaires Réglementaires Business Solutions MDS/MMS EMEA, en charge pour la région EMEA des activités réglementaires relatives aux produits du Business Medication and Delivery Solutions et du Business Medication Management Solutions, intégrant le plus gros portefeuille produits de BD.

Job Description

Mission

Description de la mission principale :

  • Création d’un outil PowerBI pour visualiser et consolider l’ensemble des travaux et activités de l’équipe Réglementaire Business Solutions.
  • Evaluation de l’étiquetage pour l’ensemble des produits du portefeuille MDS et MMS au niveau MDD et MDR, consolidée avec les activités CRAF (Change Request Approval Form)
  • Support des demandes clients pour les produits des gammes MDS et MMS

Missions secondaires en fonction de la charge de travail :

- Participations aux activités de marquage CE MDR et mise à jour de la documentation technique.

- Revue réglementaire des documents promotionnels avant leur diffusion en Europe.

Votre Profil

Formation : Etudiant en Master avec une spécialisation Affaires Réglementaires ou industrie des produits de santé

Aptitudes :

- Excellent niveau d’anglais à l'écrit et à l'oral impératif (communication exclusivement en anglais)

- Rigueur et organisation

- Maitrise des outils informatiques

- Aisance relationnelle en réunions

- Connaissances élémentaires sur le cycle de vie d’un produit, MDR, ISO13485

Required Skills

Optional Skills

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Primary Work Location

FRA Grenoble

Additional Locations

Work Shift

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Success Profile

What makes a successful Regulatory Affairs Professional at BD? Check out the top traits we’re looking for and see if you have the right mix.

  • Analytical
  • Collaborative
  • Communicator
  • Persuasive
  • Problem-solver
  • Skilled presenter

Advancing the world of health™

BD is one of the largest global medical technology companies in the world and is advancing the world of health™ by improving medical discovery, diagnostics and the delivery of care. BD helps customers enhance outcomes, lower costs, increase efficiencies, improve safety and expand access to health care.

At BD, we are committed to global inclusion and diversity. Increased inclusion and diversity drives innovation, allows us to better understand patient and customer needs, and ultimately makes BD the best possible place for all associates to thrive.


Brian Carney
Staff Regulatory Affairs Specialist

I love working with high powered leaders on a day to day basis who are respectful to my opinion and who I was never exposed to in my past job.


Robin Cassell
Global Regulatory Operations Labeling Specialist

I have been trusted in my ability to lead exciting and challenging projects with excellent upper management support. This in-turn has allowed me to grow and expand my regulatory knowledge that I believe will lay as a foundation to build my Regulatory career on.


Nikita A Mahendra Kumar
Senior Regulatory Affairs Specialist

BENEFITS

Healthcare

Healthcare FSA

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Retirement Plans

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Paid Time Off

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