This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message
NextPharmaJob.com for pharmaceutical industry jobs
NonStop Recruitment
NextPharmaJob.com is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Home-based flexibility, RA Manager
Hampshire
Operations Manager - Supply Chain (Belgium)
Belgium
Operations Manager - Supply Chain (Switzerland)
Switzerland
Chef de Projet Clinique - Dispositfs Médicaux
France
Product Manager - Dental Materials- Europe
Switzerland
More...

To receive a FREE weekly email alert of all the latest pharmaceutical industry jobs added to our database enter your email address below.

Submit | Tell me more...

Sister sites:
Our sister site Our sister site
Partner sites:

At Burntsky Limited we work with a number of third parties in order to maximise the reach of the jobs posted with us including but not limited to:

JooblePartner Jooble
UK Jobs
Science Jobs

Job Details
This job has expired. Click here to view similar jobs.

Associate, Regulatory Projects - Medical Devices - Austria



Business Type: Medical Devices Company
Job Type: Medical Devices
Job Level: Experienced (non manager)
Position: Full Time
Location: Austria
Reference: MT - 62094 - 1
Closing Date: 24/07/19
Job Details:

Main Tasks

  • Lead, organize and support key regulatory projects / tasks and regulatory compliance initiatives
  • Support preparation of regulatory submissions, license renewals and registrations to international authorities
  • Organize and maintain regulatory documentation to meet regulatory requirements
  • Provide regulatory input to product development projects

Requirements

  • Education and/or experience equivalent to a Master''s degree, preferably in a legal, science or engineering discipline, with a health science or biomedical component e.g. HTA, public health, clinical research, regulatory affairs
  • At least 2 years medical device or regulatory affairs work experience is strongly preferred, graduates with any biomedical related experience e.g. in pharma industries, clinical research or health technology assessment are also welcome
  • Knowledge of the new Medical Device Regulation (EU) 2017/745 and project management skills is an advantage
  • Excellent English (spoken and written) is required, advanced German strongly preferred
  • Eager to learn, attention to detail, proven problem-solving & organizational skills, as well as a collaborative personality



Posted: 17/07/2019 | NPJ Ref: 238834
line graphic

Compatible with:

JobMate   Broadbean   Idibu

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing




Credit cards image