Vi søger medarbejder til Pharmacovigilance – Stillingen er besat

Har du lyst til at arbejde i et specialiseret konsulentfirma hvor du får mulighed for at dygtiggøre dig? Har du lyst til at yde en god service til vores kunder? Er du træt af at sidde i møder? Vil du hellere bare lave dine opgaver? Har du mod på at blive oplært til Deputy QPPV? Så søger vi en medarbejder til vores Pharmacovigilance team. Du kan læse mere om stillingen her:


Billev Pharma experiences increasing demand for our Pharmacovigilance services and our team working with Pharmacovigilance is growing

Lisbeth Bonde Jensen, M.Sc. Pharmacy and Pg. Diploma in Pharmacovigilance, has been with us since April 2016. Lisbeth has more than 10 years of experience with Pharmacovigilance from the pharmaceutical industry.

Are you interested in working with our highly skilled and specialised Pharmacovigilance team? Then contact us at

We value our old and new clients

And have assisted some of our old clients with regulatory affairs and pharmacovigilance since Billev Pharma was founded in 1978 – some on a daily basis and others when they need our help.

With the growth of the company we continue to build relationships with new clients. We offer a wide range of services and in first half year of 2017, we have worked on assignments, such as:

·       Upgrading of quality management system to GMP standard

·       Assuming temporary responsible person/quality responsible for two companies holding GDP authorisation

·       Translating product information for both generics and brand leaders

·       Writing the quality part for a veterinary medicinal product to be submitted in the centralised procedure

·       Writing and/or compiling 3 human DCPs.