Skip to main content
Identification de l’offre d’emploi R-508900 Date d’affichage 02/05/2025

Job Description Summary

Working closely with the Senior International Regulatory Affairs Manager, the International Regulatory Affairs Specialist will be responsible for supporting international regulatory affairs registrations on medical devices and in vitro diagnostic devices across the globe.

Job Description

This position is responsible for the creation, identification, collection and entry of regulatory affairs information of medical devices.  Support related regulatory affairs activities for international regulatory submissions, execution and management of country registration request.  Requires strong organizational skills, communication and ability to manage multiple task. 

Essential Responsibilities:

  • Create, submit and maintain product registration request for submission
  • Review and approve documents required for submission
  • Maintain up to date metrics with product registration request and submission schedule
  • Track regulations applicable for medical devices in designated countries
  • Collaborate with regional RA teams, using internal systems as applicable, to obtain strategic alignment for submission and schedules for each country
  • Input and maintain data, including licesnse and registration records into internal regulatory databases
  • Ensure communications regarding request from platform RA teams and regional RA teams are responded to in a timely manner

Qualifications:

Educational Background: 

B.S. degree or higher in a technical discipline, preferably in computer science, engineering, bioengineering, biology, or chemistry.

Professional Experience: 

3-7 years Regulatory Affairs experience in medical device companies including international product registrations, new product development and sustaining engineering.

Knowledge and SkillsKnowledge

  • Working knowledge of 510(k) (for both medical devices), MDD 93/42/EEC, MDR 2017/745 and working knowledge of 21 CFR 820 -Quality System.

Skills

  • Proficient in using Microsoft Word, Excel and PowerPoint.
  • Proficient in English
  • Strong communication Skill, both oral and written
  • Strong project management skills
  • Must be able to handle multiple tasks and attention to detail.
  • Self-motivated, comfortable with working with people remotely

Organized, analytical think

Required Skills

Optional Skills

.

Primary Work Location

IND Bengaluru - Technology Campus

Additional Locations

Work Shift

Postuler

Working in

Bangalore

Take a look at the map to see what's nearby.

EXPLORE LOCATION

Recommend
to a friend

Approve
of CEO

"Purpose driven company where associates work every day to make healthcare better. A lot of great initiatives going on to make BD the best MedTech company in the world."
Anonymous, Franklin Lakes, NJ

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.

En cochant cette case, vous reconnaissez avoir lu notre politique de confidentialité et consentez à recevoir des communications électroniques de la part de BD.

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.