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Se dine JobagenterSafety Medical Writer in Global Safety, (1-year parental leave cover)
Are you interested in working in drug safety and pharmacovigilance and helping to ensure the safe and effective use of medicines? Would you like to join a Safety Medical Writing team responsible for preparing medical documents for all Ferring products to ensure patient safety?
Our team is a dynamic group of six talented individuals with diverse experiences and skills. Collectively, we possess expertise in medical communication and writing. We strive for simplicity and efficiency in our processes and collaboration with stakeholders across the global Ferring organisation.
(Senior) Director, Biotherapeutic Screening
Would you like to lead a department deeply involved in building our early research portfolio of monoclonal antibodies and other biotherapeutic modalities?
You can look forward to working at our state-of-the-art International PharmaScience Center (IPC) in Copenhagen, where we have invested in the newest laboratory technology, including laboratory automation, high-content imaging, and advanced flow cytometers.
Experienced Laboratory Technician
Are you skilled in cell biology techniques and like to use a large variety of laboratory methods? Would you like to apply your skills across different therapy areas including Reproductive Medicine, Uro-Oncology and Gastroenterology?
In this role you will be challenged with new assays where you can apply your skills and experience and – more importantly – where you will be trusted and empowered to find solutions. Your ideas are welcomed and if you need help, you are surrounded by experienced and highly skilled colleagues who are eager to support you.
Global Regulatory Affairs Manager
Do you want to spend your workdays in a multicultural corporate environment where you can continuously develop your skills and help find innovative solutions to regulatory challenges?
Your new team will be Global Regulatory Affairs CMC Biologics, responsible for all regulatory CMC activities during development, registration, and approval, as well as CMC lifecycle activities for products within our portfolio.
As a Global Regulatory Affairs Manager, you will be responsible for CMC activities related to the life cycle management of products within our Biologics portfolio.
Bioanalytikere til Steno Diabetes Center Copenhagen
Er forskning, udvikling og ny teknologi dit interesseområde?
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Det er en god idé, at du opretter et CV, så virksomheden let og med det samme får en god forståelse af dig og din profil.
Det er en god idé, at du sætter dit CV online, så virksomheden let og med det samme får en god forståelse af dig og din profil.
Det er en god idé, at du opdaterer dit CV, så virksomheden let og med det samme får en god forståelse af dig og din profil.