Our highly valued colleague Majbritt Eichmeier Hansen has been with us since March 2011 so this year we are celebrating her 10 years anniversary. Majbritt began her career in Regulatory Affairs, today she specialises in Pharmacovigilance. In 2015 Majbritt was
Promotion
We are happy to announce the promotion of Katrine Schuster Ovesen from Officer to the position of Regulatory Affairs Manager. Katrine has been with us for 6 years, starting as a student worker. She has shown an impressive ability to
Our RA team is growing and continues to in 2021…
Anne Ravnholdt Høcker joined Billev Pharma’s RA team in September. Anne has more than 20 years’ experience with writing and reviewing analytical and pharmaceutical documentation for MAAs and variations. Anne had a strong wish to work part-time but at the
Extension of our RA team with an experienced Regulatory CMC specialist
Karina Rebild joined Billev Pharma as a Regulatory CMC Specialist in August. With her more than 30 years’ experience – including sterile production and regulatory lifecycle management – she brings valuable knowledge to our RA team, which currently counts 15
Vi søger erfaren RA specialist – Stillingen er besat
Vi søger specialist til vores RA team, som hurtigt vil kunne arbejde selvstændigt med opgaverne. Har du flere års erfaring med registrering? Søger du nye udfordringer? Ved du en masse om vedligeholdelse af registreringer for humane lægemidler herunder udarbejdelse af
Konsulenter i en Coronatid
Corona betød en stor omvæltning for manges arbejdsliv. Men ikke for vores, for vi fortsatte bare det, som vi havde gjort siden vi overtog Billev Pharma i 2015, men nu i meget højere grad. Vores medarbejdere havde i forvejen mulighed
Our team has extensive experience
As of January 2020, Susanne Thiilborg and Bo Kreilgaard will hold the position of Senior Regulatory Affairs Manager and Lisbeth Bonde Jensen now holds the position of Senior Pharmacovigilance Manager. Lisbeth is also QPPV for one of our major accounts.
Vi søger erfaren Regulatory Affairs Manager – Stillingen er besat
Vi søger en erfaren Regulatory Affairs Manager, som hurtigt vil kunne arbejde selvstændigt med opgaverne. Ved du en masse om CTD, eCTD og mere specifikt om et eller flere af modulerne 1-3? Du skal indgå i et team med dygtige
Our regulatory team
As of January 2020, Karen Jensen will hold the position as Head of Regulatory Affairs and Charlotte Munk Ejlersen now holds the position as Senior Regulatory Affairs Manager. Karen and Charlotte, together with the rest of our regulatory team, achieve
We hope to meet you
29-31 January we are attending first the Pharmacovigilance Conference and then the Regulatory Affairs Conference arranged by Medicines for Europe at the Hilton Hotel, Amsterdam.