Je waarborgt dat onderzoeksprojecten naar klinische productontwikkeling , zoals vaccins tegen bijvoorbeeld Covid-19, hand- voet en mondziekte en gonorroe, voldoen aan de farmaceutische wet- en regelgeving.
Do you have strong affinity with data management and data analysis, and would you like to play a key role in late stage process development projects? In this Associate Scientist role you will be responsible for data verification and translating
these data into reportable formats and historical data mining. Interested? Apply now!
As a Laboratorium LIMS configurator you are responsible for translating documents, like stability plans, specification sheets and sample plans to clear eLIMS Master Data and configurations.
Are you a motivated candidate with strong experience in Sample management within the pharmaceutical industry? In this role as a Sample Managment Specialist (COVID-19) you will use your expertise to support the manufacturing of biopharmaceutical products including the COVID-19 vaccine. Apply now!
Are you skilled with Separations and Chemical & Physical techniques and would you like fill in a challenging position in the pharmaceutical industry? In this role as a Separations & Chemistry Specialist (COVID-19) you will use your expertise to support the manufacturing of biopharmaceutical products including the COVID-19 vaccine. Apply now!
Do you want to manage stability studies within a big pharmaceutical company? As a Stability Scientist it is your reponsibility to coordinate stability studies of novel vaccines during clinical development. Keep reading to find out more!
Are you a motivated hbo candidate with up to date knowledge of GMP regulations and would you like to gain Quality Assurance experience? In this role as a QA Support Officer you are responsible for Batch documentation review and you provide advice to departments regarding GMP aspects. Interested? Apply now!
Jouw kennis over (bio)analytische chemie pas je toe om de kwaliteit binnen de Bioassay afdeling te monitoren en te verbeteren. Je behandelt complexe deviaties, events en
change controls. Je werkt aan verbeterprojecten en schakelt hiervoor
veel met verschillende afdelingen in de organisatie. Geïnteresseerd
geraakt? Solliciteer direct!
Are you a communicative person with excellent project management skills who would like to gain experience in regulatory affairs? Then, this position as a Regulatory Affairs Assistant might be interesting for you! In this role, you will ensure compliance with local regulatory requirements, the national and international guidelines, and the company policies for an internal project.