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 for mindst 1 hjemmearbejdsdag om...
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. Lisbeth,...
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 kollegaer. Vi tilbyder alsidige opgaver, en...
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 high quality...
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.
Poor-quality translations may delay your time to market
Maria Brogaard is our state-authorised translator who has been with us for more than 15 years. Maria provides high-standard translations and proofreading of product information and all other documents in connection with regulatory procedures and pharmacovigilance in...
We now cover all areas within regulatory affairs
In February 2019 Susanne Thiilborg, Ph.D.Pharm., began a position as Regulatory Affairs Manager with Billev Pharma. Susanne has more than 20 years’ experience within analytical chemistry from the pharmaceutical company Lundbeck. Susanne accounts for all possibilities...
Promotions
We are happy to announce the promotion of Charlotte Lindorf Eriksen and Sana Iqbal from Officer to the position of Manager. Charlotte and Sana have been with us for 4 years and have both shown an impressive ability to upskill rapidly.