Vigilance - Medical Device Global Company

Vigilance - Medical Device Global Company

Medical technologies save lives, improve health and contribute to sustainable healthcare. One of the world's major players in this field is looking for an experienced Quality/Regulatory specialist to join an expanding team and to enjoy the benefits of a growing company by having the advantage of career progression sooner than usual.

It is an extraordinary opportunity to join this worldwide known organsiation and to specialise in different product areas you are passionate about. This role will give you the chance to progress into a team leader positions or into Sales, if this is what drives you. The company is massively growing and it is an exciting time to join, you will actively participate in the succes of the products and you will make yourself visible in the market.

If you believe that you want to have a greta impact on people's lives and improoving general health is one of your passions, do not hesitate to contact me!

Basic Requirements:

* Completed Bachelor's degree in natural sciences, engineering, and clinical OR medical advanced degree
* Experience within the Medical Device industry with a Quality/ Regulatory Affairs background
* Analytical knowledge to understand and solve issues
* Good command of English and German
* Post Marketing Surveillance experience is an advantage

For a confidential discussion about this role and to take a positive step to your next role call me and I will be happy to discuss further details with you or anyone from your network, whom you recommend.
You can contact me at Reka Peterfi: +41 435 080 817, extension: 3344 or email me your CV in Word format: R.Peterfi@nonstop-pharma.com.
Nonstop is one of the largest and fastest growing specialized life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licenses across Europe. Please visit our website for a full list of the niche markets we cover.

Pharmacovigilance, drug safety, adverse reaction, traditional medicine, signal, side effect, risk management, prescription-event monitoring, Pharmacoepidemiology, efficacy, ICH, drug alerts, counterfeit medicine, clinical, case-control study, adverse reaction/event, ADR, UMC, ICSR, case management, PSUR, Drug safety associate, PV associate, Safety Leader, drug safety officer, Pharmacovigilance/Drug Safety Associates or Officers, Pharmacovigilance/Drug Safety Managers, Pharmacovigilance/Drug Safety Directors, Head of Pharmacovigilance/Drug Safety, Pharmacovigilance/Drug Safety Physicians, Pharmacovigilance/Drug Safety Auditors, Pharmacovigilance Quality Assurance or Compliance, Pharmacovigilance/Drug Safety Systems Specialist, ArisG/Argus Experts, Qualified Persons for Pharmacovigilance/QPPV, Pharmacovigilance/Drug Safety Medical Writers