Vacatures 1 tot 10 van 53
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Grafton Recruitment - Amsterdam
years of experience. Has drug safety experience in a post-marketing environment.Possesses comprehensive knowledge of EU safety regulations and Good Pharmacovigilance Practices.Is an effective communicator with strong attention to- Volledige vacature bekijken
Internship Drug Product Development and Delivery
Randstad Nederland - Leiden
Do you want to develop yourself at one of the largest organizations dedicated to bringing substantial innovation to global health? Then this is your chance! Johnson & Johnson is a global Healthcare company, full of entreprene- Volledige vacature bekijken
Luba - Amsterdam
Over het werkAls operator speel je een cruciale rol in het productieproces van bloedplasma en gerelateerde producten. Je voert verschillende productiehandelingen uit volgens strikte kwaliteitsnormen en gestandaardiseerde proc- Volledige vacature bekijken
Iqvia via Talent - Zwolle
is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policiesMarken via Talent - Lijnden
SOP’s (if necessary)Compliance with and work according to MARKEN policies as well as applicable MARKEN quality standardsCompliance with all health policies and safety -conscious work, treatment of all substances with relevantSenior Programming Associate / Programming Manager
Genmab via Tables - Utrecht
Drug Safety , Medical, Clinical Pharmacology and Biomarker functions by developing and writing corresponding SAS or other programs.Responsibilities/tasks - including but not limited to:Reviews CRFs for adequacy andIqvia via Talent - Nijmegen
is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policiesIqvia via Talent - Groningen
is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policiesIqvia via Talent - Breda
expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under theIqvia via Talent - Tiel
expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under theTechnical Transfer Project Manager
Thermo Fisher Scientific via Talent - Tilburg
knowledge of Good Manufacturing Practices and Food and Drug Administration (FDA) compliance knowledge. Effective social skills, and the ability to collaborate with influence and empower cross-functional team members. Ability to meetKelly Services via Talent - Amsterdam
microbial based production of recombinant proteins, vaccines and live microbials as drug substance and drug product. We are currently looking for a: Technician (Downstream Processing / mRNA) Benefits Employment: A challenging and