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
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.
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 an environment where
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 and reviews the relevant
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
We started 2019 by welcoming 3 new employees in our Billev Pharma team
Trine Lorentzen, M.Sc. Pharm., filled the recently established post as QA Manager. Trine has several years of solid experience with Good Distribution Practice (GDP) and the function as Responsible Person. Are you facing an inspection? Are you struggling to keep
Could you use a helping hand in your regulatory department, or do you lack the specialised staff in-house to handle European procedures?
In June 2018 Karen Jensen, M.Sc. Pharm., joined our regulatory team. Karen and our regulatory team can assist you with both European and national initial MAAs or maintenance activities. Karen is a generous co-worker and has more than 16 years
Anniversaries in 2018
In 2018 we celebrated Billev Pharma’s 40 years anniversary and also 3 times 10th anniversaries. Mette Skaarup Pedersen has been with us since 2008. Mette’s key area is proofreading and translation. Mette is highly respected among our clients for her