Job description
We offer a job as a Pharmacovigilance (PV) Consultant, in which you will:
– work in an international environment of pharmaceutical and medical device industry
– write and review pharmacovigilance-related documents (eg. PSUR, RMP, SOPs, PSMF)
– ensure compliance with safety-related marketing authorisation commitments and obligations
– monitor and interpret safety findings from literature
– manage and maintain pharmacovigilance databases
– provide input on safety for clinical development
– be mentored by Zwiers
– live up to the Zwiers “professional approach with a personal touch” spirit

You have:
– preferably, a PhD in Pharmacy, Medical Biology, Life Sciences
– minimal 2-3 years of experience in the pharmaceutical industry and PV
– knowledge of pharmacovigilance, pharmacovigilance systems and GVP modules
– eager to learn, develop and excel
– the ability to handle deadlines and changing priorities in a dynamic environment
– writing and reviewing skills (English)
– the ability to communicate effectively based on scientific knowlegde

Zwiers Regulatory Consultancy offers a fulltime job, but is willing to discuss a part time contract
Salary will depend on education, knowledge and experience

For further information you can contact Alex Zwiers, CEO, at tel. +31 (0) 610489150.
We look forward to your application. You can apply via email: