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6 jobannoncer matcher din søgning 6 jobannoncer fundet
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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.
Senior Regulatory Affairs Manager
This pivotal role will involve navigating the complex regulatory landscape associated with technologies for the production of hydrogen, its derivatives and other related technologies. This critical role will also involve ensuring compliance and strategically influencing regulatory development to support our mission.
The ideal candidate will have a deep understanding of energy regulations, a passion for sustainability, and the expertise to guide our company through the evolving regulatory environment.
Nordic Account Manager
In the exciting role as Nordic Account Manager, you will work with SSI Diagnosticas full product portfolio and sales towards the clinical and industrial segments in the Nordics.
You will work with a lot of talented and engaged colleagues and will be a key player in developing and grow the Danish market. You will be working closely together with other Nordic sales reps, customer service and relevant colleagues from our production and trade product partners.
Regulatory Affairs Clinical Specialist
Due to many activities in our exciting clinical development projects, we are seeking two new colleagues to our Regulatory Affairs function.
Your key responsibilities will be to contribute with regulatory expertise to global strategies and execution within your assigned project(s). You will be the regulatory responsible in the clinical trial teams and provide regulatory guidance and support for the planning, execution, and reporting of clinical trials worldwide.
Operatør/miljøassistent til EM (Miljømonitorering)
Vil du være med til at sikre, at miljøet i vores produktion følger krav og regler?
Process Technician for Research and Development
Do you become energized by doing something out of the ordinary and do you see yourself thrive in a start-up environment?
