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Weekendarbejde i Miljølaboratorium

Eurofins Miljø i Vejen søger nye kolleger over 18 år til weekendarbejde i laboratoriet. Vi søger dig, der studerer naturvidenskab eller er uddannet laborant, og som har har interesse for at arbejde i et laboratorium, hvor fleksibilitet, alsidighed og troværdighed er i højsædet.

Dine primære arbejdsopgaver vil være vedligehold af udstyr, fejlfinding og opsætning af prøver på GC-MS + GC-MS/MS og LC-MS/MS.

Project Leader – process/hydrogen safety

Do you want to apply your skills to promote a fast and safe transition of the energy and transportation sectors away from carbon-based fuels?

You will be leading diverse teams of experts to deliver state-of-the-art results to our partners in the hydrogen sector, working on some of our largest fire safety projects.

We have great offices and facilities, and you get good staffing conditions, such as pension scheme, dental insurance, and health insurance. We have an active staff and art association, and our chefs cook delicious food for us daily.

Battery specialist

Do you want to apply your skills to promote a fast and safe transition of the energy and transportation sectors away from carbon-based fuels? Do you have experience working with or developing battery technologies?

As our new Battery Fire Specialist, you will provide expertise on Li-ion batteries and other upcoming technologies to the team. You will be part of projects performing risk analyses, battery fire tests, and fire safety design for clients and in R&D contexts.

Senior Technical Writer - Regulatory (CMC)

You will join the Technical Writing team within Global Regulatory Affairs. We are responsible for global regulatory CMC writing of regulatory documents in applications for new approvals, worldwide market expansions, and product lifecycle activities. We work with a variety of pharmaceutical products, including small molecules, peptides, biologicals, recombinant products, and gene therapy.

Stepping into an informal and collaborative environment, you will have close interfaces with many different disciplines, including Global Pharmaceutical R&D, manufacturing sites, Product Supply, Quality Assurance, Ferring affiliates, and development sites around the world.

Senior Clinical Scientist

Do you want to:

• Execute clinical evaluation and documentation activities, including clinical input to PMCF and PMS.
• Provide clinical support to global registrations.
• Support and drive ad hoc clinical activities and problem solving

The main responsibilities of our Clinical Development team are to drive the clinical strategies to ensure timely execution on clinical deliverables to support regulatory submissions and commercial strategies.