דרושים » רפואה ופארמה » דרוש /ה רוקח /ת מתחום ה- Pharmacovigilance למשרת QPPV בחברת רגולציה מובילה

Requirements:
* BSc in Biomedical Engineering (or equivalent scientific degree).
* At least 3 years of experience in regulatory affairs in the medical devices industry.
*  English - Fluent reading and writing.
* Experience as a QA Engineer in a Medical Device company - big advantage.
* Ability to multi-tasking, prioritizing, accuracy and thoroughness.
* Ability to work under pressure and in tight schedules.

Requirements:
Education: o BSc in a scientific area, (Bio-medical or Quality Engineering - an advantage) or acknowledged regulatory course graduate Job skills: o 2-4 years medical device/pharmaceutical post market experience o Knowledge and experience with the following regulatory systems: EU / Canada /US - advantage to other regulation o Minimum 2 years management experience o Strong verbal and written communication skills o Good technology expertise is essential o Experience in front of the authorized authorities o Understanding of risk management disciplines Language skills English – very high level, verbal and written Other o Ability to work under pressure and in tight schedules o Ability to work in Multidisciplinary environment o Strong interpersonal skills and demonstrated ability to effectively communicate technical content o Strong attention to detail and accuracy oriented o Good analytical skills Other o Ability to work under pressure and in tight schedules o Ability to work in Multidisciplinary environment o Strong interpersonal skills and demonstrated ability to effectively communicate technical content o Strong attention to detail and accuracy oriented o Good analytical skills