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.
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.
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--We are the makers of possible--
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.
--Why join us?--
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
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 CedexAdditional 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 AnnualSuccess 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.