Medical device registration and regulatory affairs

The ideal candidate will have experience in the medical devices industry and a deep understanding of regulatory affairs and compliance.

Responsibilities include:

  • Assist in coordinating/preparing and reviewing regulatory submissions for Delta’s products and following up on customs clearance whenever needed.
  • Keep track of the progress of regulatory submissions to Complete regulatory submission forms within the assigned time frame.
  • Handling all medical device related communications
  • Coordinating the paperwork between suppliers and EDA
  • Ensuring compliance with all necessary regulations
  • Maintain adequate records for suppliers documents.

 


 Bachelor's Degree in Pharmaceutical Sciences/ Vet./ Science.Experience in Medical Devices is a must2-5 years of experience in a similar positionV. Good command of English language written & spokenProficiency in MS Office: Word, Excel, PowerPoint Work conditions: Location: Mokattam, CairoWorking days: From Sunday to ThursdayWorking hours: from 09:30AM to 05:00PM  
Post date: Today
Publisher: Wuzzuf .com
Post date: Today
Publisher: Wuzzuf .com