Post Market Surveillance Specialist - Med. Device

Post Market Surveillance Specialist - Medical Device

Are you looking for a chance to join a globally known Medical Device company?
Would you be excited to know that this role is actually a door opener for several departments within the Company?

My client is looking for an experienced Vigilance specialist with a strong background in the areas of Quality/ Regulatory Affairs to join their team now.
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 think that this sounds like you, get in touch and I will provide you further details!

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