Medical Director

Currently, we are looking for a new Medical Director who has a medical background, experience from conducting and designing pharmaceutical industry trials.

We are looking for a self-driven team-oriented colleague with the capability to lead cross-functional teams towards innovative solutions for delivering the highest standard clinical development trials for our drug candidates.

Barselsvikar til complaint investigation team

Find din indre detektiv frem, og bidrag til sikkerheden i behandling af patienter med blodkarsygdomme.

Du skal sætte dig ind i, hvad kunden har oplevet i de forskellige hændelser, undersøge returnerede produkter og lave risikoanalyse ud fra de informationer, du har tilgængelig.

Du får 11 søde, hjælpsomme og dygtige kollegaer er klar til at modtage dig i teamet.

Erfaren CAPA Specialist med stærkt kvalitetsmindset søges til Medico virksomhed

CAPA-processen er en vigtig hjørnesten i vores virksomhed. Vi søger derfor en rutineret kollega, der har tung erfaring med problemløsning omkring afvigelser i alle dele af QMS.

Du får ansvaret for at drive CAPA’er fra opstart til afslutning, ligesom du medvirker i planlægningen sammen med Procesejer, og faciliterer de forskellige trin i CAPA-processen. Du er ansvarlig for CAPA review og medvirker til at sikre kvalitet i de valgte løsninger.

Clinical Scientist

Join GE HealthCare to help develop our growing team in Clinical Development. This is your opportunity to become part of an innovative team where your work has a real impact on people’s lives around the world.

Our main responsibilities are to drive clinical strategies successfully, i.e., leading and maintaining products throughout their entire life cycle management.

We are an international team who values cultural and personal diversity in an informal, friendly, and respectful atmosphere.

Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)

At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.

The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.

You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.

Farmaceuter til Regulatory Affairs

Vi mangler hurtigst muligt 2 Regulatory Managers med interesse for og meget gerne erfaring med Regulatory Affairs. Stillingen byder på et bredt udvalg af opgaver, og du vil også få mulighed for at arbejde med marketing compliance.

Du skal bl.a. lave compliance review af marketingaktiviteter og -materialer for den farmaceutiske industri og anmeldelser til Etisk Nævn for Lægemiddelindustrien samt oversættelser af regulatoriske og medicinske dokumenter (dansk/engelsk).