Identification de l’offre d’emploi R-520293 Date d’affichage 10 de juliol 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
  • Glassdoor Reviews and Company Rating

Responsibilities

Job Description Summary

The Associate Director, Regulatory Affairs, Specimen Management (SM) reports directly to the Vice President, Regulatory Affairs, Specimen Management. This position is responsible for regulatory activities and personnel supporting the Specimen Acquisition (SA) business growth and sustaining agenda. The role includes responsibilities for directing and evolving the regulatory strategy for the SA Platform, interacting with regulatory authorities and Notified Bodies to ensure SA’s growth and continued right to operate, supporting SA New Product Development and sustaining efforts, identifying and championing innovative regulatory approaches, collaborating within the RA function and cross-functionally to drive success, and leading and inspiring a team of regulatory affairs associates. This role will directly engage with both the SM RA Leadership Team and the SA Platform Leadership Team.

Job Description

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.

We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a makerof possible with us.

BD’s Specimen Management Regulatory Affairs organization is the keystone of Specimen Management’s product registration efforts, connecting internal and external stakeholders to deliver safe, effective, and innovative diagnostic collection and care devices to patients and customers in alignment with business priorities and global regulations.

About the Role:

In this role you will lead regulatory strategies and ensure compliance, driving growth and innovation in our team.

Key responsibilities will include:

  • Leading BD’s Specimen Management Regulatory Affairs team for the Specimen Acquisition Platform.
  • Collaborating with SM business leaders and functions to drive initiatives and execution.
  • Aligning regulatory strategies with business plans to foster growth, innovation, and profitability.
  • Developing and implementing policies to ensure compliance with FDA, EU MDR, and international requirements.
  • Acting as the primary contact for regulatory agencies, providing documentation, and ensuring comprehensive review.
  • Leading regulatory audits and preparing regulatory records and documentation.
  • Advocating favorable regulations for timely patient access to products.
  • Driving SM RA strategies for New Product Development and sustaining efforts.
  • Building strong regulatory capabilities and leadership within the team.

About you:

You are a problem solver who excels in simplifying complex issues within broader business contexts, with a proven track record in regulatory submissions and negotiations. Your leadership encourages high-performing teams, embraces diverse perspectives, and uses innovative solutions to drive growth and compliance.

Education and experience required:

  • At least 10 years of experience in the IVD/medical device field with growing responsibility.
  • Minimum 3 years of management experience.
  • Proven success in developing systems for regulatory submissions and acquiring timely approvals.
  • Extensive knowledge of global regulatory strategies and experience with FDA Class I and II products.
  • Significant experience with EU MDR or equivalent experience and Notified Body engagements.
  • Demonstrated ability in regulatory advocacy, policy, and recruiting high-performance RA teams.
  • Success in large, matrix-managed organizations, partnering with MA, QA, and R&D.
  • Comprehensive knowledge of regulatory requirements in the U.S., EU, and other international markets.

Click on Apply if this sounds like you!

Why Join Us?

A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.

You will learn and work 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. And through the organization’s investment in BD University, you will continually level up your tech skills and expertise.

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.

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

Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to 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, and other legally-protected characteristics.

Required Skills

Optional Skills

.

Primary Work Location

USA NJ - Franklin Lakes

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 based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles.

Salary Range Information

$177,700.00 - $293,100.00 USD 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

Employer Matching

Tuition Reimbursement

Paid Time Off

Location

Collaborative Culture

Competitive Compensation

Awards &
Recognition

Travaillant dans

Franklin Lakes

Jetez un coup d'œil à la carte pour voir ce qui se trouve à proximité.

Ne manquez pas cette opportunité

Assurez-vous de voir passer l’emploi parfait pour vous dès qu’il sera affiché. Inscrivez-vous à notre service de notification d’offres d’emploi dès aujourd’hui.

Interessé(e) parRecherchez une catégorie et sélectionnez-la dans la liste des suggestions. Recherchez un lieu et sélectionnez-en un dans la liste des suggestions. Enfin, cliquez sur "Ajouter" pour créer votre alerte d'emploi.Recherchez une catégorie et sélectionnez-la dans la liste des suggestions. Recherchez un li

Joignez-vous à notre banque de talents

Joignez-vous à notre banque de talents

Téléchargez votre CV pour aider notre équipe de recrutement à identifier un poste à votre mesure. Si une occasion se présente, l’équipe communiquera avec vous.

AVIS DE FRAUDE DE BD

Nous vous invitons à prêter attention aux offres d’emploi potentiellement frauduleuses sur d’autres sites Web ou aux messages électroniques ou textuels de recrutement suspects qui tentent de recueillir vos renseignements confidentiels. Si vous craignez qu’une offre d’emploi chez BD, CareFusion ou C.R. Bard soit une escroquerie, nous vous invitons à vérifier son bien-fondé en recherchant l’offre sur la page des carrières ou à communiquer avec nous à l’adresse ASC.Americas@bd.com.