Staff Engineer – Global Regulatory – Medical Devices

  • Company:
  • Location:
  • Salary:
    negotiable / month
  • Job type:
  • Posted:
    3 weeks ago
  • Category:
    Manufacturing/Industrial | Healthcare

Skill: regulatory submission , regulatory; Exp: 2-3 years; Job Snapshot Employee Type Full-Time Location Gurugram Job Type Engineering Experience Not Specified Date Posted 9/25/2018 Job ID 28174BR Job Description Working experience of Regulatory submissions such as FDA (IDE/510k/PMA) and EU (CE Technical file and dossier) Working experience with R&D teams in regulatory area Regulatory Submission knowledge of International is a plus Accountable for regulatory strategy and deliverables to support New Product development both domestically and internationally Interaction with cross functional business partners for regulatory guidance Proactively assess policies and emerging issues related to Medical Devices and work closely with divisions to develop and implement strategies to address the impact from regulatory perspective Good judgement with ability to make timely and sound decisions ,10-Aug-2018 Work From Home No Travel Percentage None

Drug Regulation


Experience: 2-3

Function: Biotech / Pharma / R&D