Product Surveillance Scientist in Neuchatel

Filipa Lessa, Basel Professionals Health Care & Life Sciences
jetzt bewerben

job details

Neuchatel, Neuenburg
Life Sciences
Filipa Lessa, Basel Professionals Health Care & Life Sciences
058 201 55 50
jetzt bewerben


                                                Job Description                                                                                                                                                                                                                                                                                                                                           



Our client, a leading international tobacco company, with seven of world’s top 15 brands, including the world’s number one brand is looking for a


Product Surveillance Scientist



Location: Neuchatel area, Switzerland Contract:1 year with possibility of extension

Start date: asap


Manages assigned safety and surveillance activities occurring in post-market setting for all applicable reduced-risk products. Leveraging well-established standards, methods and knowledge acquired in the highly regulated drug/medical device environment to the new area of tobacco product assessment requires agility, dealing with ambiguity and learning on the fly skills.


  • Ensuring the collection of adverse events throughout the different collection channels
  • Validating and ensuring the timely transfer of each adverse event to the case processing team and managing the documentation
  • Acting as a key player for any adverse event case clarification needed for case processing and liaising with the collection channel
  • Driving monthly reconciliation of all adverse events received from the post-market setting
  • Performing regular adverse event monitoring and ensuring timely medical assessment
  • Keeping working documents for operational activities up-to-date
  • Organizing and conducting safety training for successful implementation of collection channel


  • 3-years experience in medical safety/ pharmacovigilance as safety associate
  • Good knowledge in EU pharmacovigilance (GVP)
  • Experience in using a Safety database (e.g. Argus)
  • Very detail-oriented
  • Excellent organization, communication, and inter-personal skills
  • Bsc in Life Science or equivalent acquired by training/experience
  • Experience in developing/maintaining PV processes and good knowledge in Good Clinical Pratices (GCP) would be beneficial


We are looking forward to receiving within your application:

  • your CV in English
  • latest Work Certificates
  • your Motivation Letter 
  • ID/passport copy
  • Copy of Work Permit



For more information and your application, please contact:    

Filipa Lessa Professionals Life Sciences Recruiter

Randstad (Suisse) SA T: +41 58 201 55 60