Identification de l’offre d’emploi R-501198 Date d’affichage 13 d’octubre 2024

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 function of this role is to combine knowledge of scientific, regulatory, and business to drive projects forward based on the overall global regulatory strategy to executable plans and the coordination of cross-functional team efforts.

The individual will serve as the primary project management point of contact and partner with the Consumables and Infusion System RA teams to ensure Regulatory functional plans are aligned with the IPD program objectives and commitments. The individual will work closely with other key cross-functional partners such as R&D, Commercial Marketing, Quality, Medical Affairs and Operations.

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.

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!

Our vision for Regulatory Affairs at BD

The Regulatory Affairs team is helping to ensure speed to market for BD’s innovative medical technologies by having an acutely patient-centric mindset.

Main responsibilities will include:

  • Translate regulatory requirements and strategy into an executable plan at a level of detail that allows teams to understand what is critical at any one time, proactively identify and mitigate risks, and exploit meaningful opportunities for acceleration.
  • Provide strong operational leadership to Regulatory and program teams, providing scenario and visualisation support driving rapid and informed decision making, challenging status quo and fostering impactful innovation
  • Participate to the review of process/product changes, labelling, claims, product complaints, A&Ps (Advertising & Promotional materials), etc., to determine the need for any regulatory activities and to ensure compliance to international requirements
  • Ensure coordination of critical regulatory information and team communications to ensure timely and accurate dissemination of the regulatory strategy and operational status throughout the team including co-development partners and/or other external partners, as required.
  • Drive process improvements and embed best practices from across programs and functions into supported teams.
  • Build value proposition through continuous refinement of delivery, prioritizing and focusing on areas of the highest impact and opportunity, and actively leading efforts to enable enhanced capabilities and impacts.
  • Support and facilitate activity, resource and cost planning across the R&D project portfolio, as required.
  • May attend to audits performed by internal and external authorities to represent RA positions and processes.
  • Drive regulatory affairs procedural updates, as needed, in collaboration with cross functional inputs.

About you

  • Degree or equivalent in engineering or scientific discipline, or equivalent proven experience.
  • Minimum of 5-7 years of experience in Medical Device Regulatory Affairs. Project Management experience required and knowledge of the regulatory framework pertaining to Medical Devices such as the MDD/MDR CE Marking
  • Knowledge of and experience in pre-market regulations including regulatory and risk management processes.
  • Good working knowledge of Design Control, Software Life Cycle, Risk Management, V&V processes
  • Solid knowledge and material experience in international registrations/approval process for medical devices
  • Strong knowledge in international standards and regulations including IEC 60601-1, IEC62304, IEC 62366 preferred.

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

Primary Work Location

GBR Winnersh - Eskdale Road

Additional Locations

IRL Limerick - Castletroy

Work Shift

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

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