Identification de l’offre d’emploi R-511472 Date d’affichage 30 de març 2025

Faites partie de quelque chose de plus grand chez BD. Ici, vous nous aiderez à maintenir nos normes élevées d'un point de vue réglementaire à tous les niveaux, avec un accent particulier sur les soumissions. Cela exige une attention aiguë aux détails, d'excellentes compétences en communication et une passion pour continuer à apprendre et à mettre à jour vos connaissances, ce que nous vous aiderons à faire avec des opportunités d'apprentissage régulières. Ici, vous utiliserez vos connaissances approfondies des réglementations et des exigences de la FDA, du Canada et de l'ISO/MDD entourant les dispositifs médicaux pour atteindre finalement un objectif unique : faire progresser le monde de la santé™. Chez BD, vous pouvez faire une véritable différence d'une personne.

  • Job Type:
    Full-Time
  • Job Level:
    Entry to Senior
  • Travel:
    Varies
  • Salary:
    Competitive
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Responsibilities

Job Description Summary

Join our team as the RA Senior Manager for the Pre-fillable Syringes Platform in our global headquarter located in Grenoble. Lead regulatory activities for new product development, ensuring compliance and cross-functional collaboration. Work closely with R&D, Quality Engineering, and Medical Affairs to develop regulatory strategies and drive innovation. Apply now to make a significant impact on our new product developments!
Candidates should have a strong foundation in engineering or research and development, particularly in design control and regulatory standards.The perfect candidate would be someone who has experience as a Regulatory Affairs (RA) Specialist or Manager, or as an R&D Manager.

Job Description

About the Role: Reporting to the Sr. Director of Regulatory Affairs, you will lead the RA team for pre-fillable syringes new product development projects. Your main focus will be on regulatory activities, ensuring compliance with standards related to new product design.

Your Key Responsibilities:

  • Lead the RA team, ensuring effective cross-functional collaboration and support throughout product development, including design control.
  • Develop and implement regulatory strategies to ensure new products meet the latest regulatory requirements.
  • Review promotional materials and ensure alignment with regulatory requirements.
  • Educate cross-functional teams on EU and FDA requirements.
  • Manage registrations with Competent Authorities and develop response strategies for regulatory questions.

About You:

  • Experience in regulatory affairs and R&D within the pharmaceutical and medical device industries, with expertise in drug-device combination products.
  • Engineering or Expertise in R&D: Candidates should have a strong foundation in engineering or research and development, particularly in design control and regulatory standards.
  • Proven track record in regulatory standards, submission dossier preparation, and interactions with regulatory authorities.
  • Strong project management, negotiation, and communication skills.
  • Extensive knowledge of U.S. medical device regulations, Good Clinical Practice standards, Good Laboratory Practice regulations, and Quality System Regulation.

Click on apply if this sounds like you!

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

To learn more about BD visit: https://bd.com/careers

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--Why join us?--

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To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.

Become a maker of possible with us!

Required Skills

Optional Skills

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Primary Work Location

FRA Le Pont-de-Claix Cedex

Additional Locations

Work Shift

At BD, we are strongly committed to investing in our associates—their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You.

Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates’ progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. 

The salary or hourly rate offered to a successful candidate is determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location.

Salary Range Information

80 700,00 € - 145 300,00 € EUR Annual
Postuler

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

401(k)/
Retirement Plans

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Tuition Reimbursement

Paid Time Off

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Le Pont-de-Claix Cedex

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