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Quality Assurance Expert for Clinical Trials
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Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeAbout the TeamWe are a dynamic and highly professional team working at the forefront of pharmaceutical manufacturing. Our team consists of 40 skilled and motivated colleagues divided into 4 teams, all based in Site Bagsværd.We are committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve, and the...
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Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeAbout the RoleWe are seeking a highly skilled and experienced QA Specialist to join our team in Clinical Trials. As a member of our Quality Assurance department, you will play a crucial role in ensuring the quality and safety of products for clinical trials. In this dynamic environment, you will work closely with our team of experts to deliver best-in-class...
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Senior Clinical Project Lead
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Senior Clinical Project Lead
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Global Sourcing Professional
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Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeJob DescriptionWe are seeking a highly skilled Global Sourcing Professional to join our team. The successful candidate will be responsible for supporting the clinical outsourcing process for Clinical Pharmacology Trials. This includes interacting with internal and external stakeholders to manage requests for proposal to signed contracts.The ideal candidate...
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Senior Outsourcing Professional
17 hours ago
Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full timeAre you motivated by the opportunity of being part of an ambitious clinical outsourcing team? Do you understand the pharma business, have a strategic mind-set, strong communication skills, and an interest in working with suppliers in the clinical drug development space? Then please keep reading as you might be our new colleague. The position As a Senior...
Quality Assurance Professional for Clinical Trials
7 days ago
In this exciting position, you will have the opportunity to make a difference in the lives of people participating in clinical trials by ensuring safe and high-quality products manufactured in compliance with legislation. Your key responsibilities will include ensuring best-in-class quality assurance of API for clinical trials in phase I, II, and III testing, challenging and approving documents related to the development, manufacture, stability, and status assignment of internal and external produced API, and ensuring that our products used in clinical trials follow the information provided to Health Authorities worldwide.