Product Surveillance Scientist in Neuchatel

Neuchatel, Neuenburg
Life Sciences
Barbara Sorce, Basel Professionals IT & Life Sciences
058 201 55 50
Jetzt bewerben


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: Neuchâtel, Switzerland

Contract: 1 year contract with possibility of extension

Department: Product Safety Surveillance

Start date: as soon as possible

Job Description :

Manages assigned passive safety & 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 era 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 liasing with the collection channel. 
•    Driving monthly reconciliation of all adverse events received from the post-marketing setting. 
•    Performing regular adverse event monitoring and ensuring timely medical assessment. 
•    Keeping working documents for operational activities up-to-date. 
•    Supporting in safety training for successful implementation of collection channel. 

Skills and Competencies : 

Must to have

•    3-yr experience in medical safety/pharmacovigilance as safety associate. 
•    Case processing, QC, reporting, tracking. 
•    Good knowledge in EU pharmacovigilance (GCP)
•    Experience in using Safety database (e.g. Argus)
•    Very detail-oriented. 
•    Excellent organization, communication, and inter-personal skills. 
•    Bsc in Life Science or equivalent acquired by trainings/experience. 

Good to have

•    Experience in developing/maintaining PV processes 
•    Good knowledge in Good Clinical Practices (GCP)

We are looking forward to receiving within your application:

  • your CV in English
  • latest Work Certificates
  • your Motivation Letter
  • the date of your availability

Apply now to be considered – Good to know you!

For more information and your application, please contact:

Mayank Chaubey

Consultant Healthcare and Life-sciences

Randstad professionals (SA)

Jetzt bewerben