Job

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  Vice President European Quality Assurance and Regulatory Affairs – Etac Group
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  Principal Compliance Professional, Global Pharmacovigilance & Clinical Development (GPCD) - ALK
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  Quality Assurance Director (Medical Devices) - Contura
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  Regulatory Affairs Manager - Contura
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  CMC Project Manager - Genmab
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  Principal Scientist - Symphogen
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  Team Lead /Clinical Project Lead (CPL) - Genmab
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  Trial Project Manager with NASH experience - Novo Nordisk
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  Hospital & Tender Manager - Orifarm
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  QA Manager - Ascendis Pharma
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  Ingeniør med håndværksmæssig uddannelse - Andreasen & Elmgaard A/S
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  Erfaren seniorkonsulent - Andreasen & Elmgaard A/S
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  Clinical Trial Manager - Genmab
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  Start-Up Lead - Genmab
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  Senior Specialist, Global Drug Safety & Pharmacovigilance Operations & Data Management - Genmab
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  Senior Regulatory Project Manager - Zealand Pharma
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  Manager - Automation & SCADA - ALK
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  Laboratory Technician - Zealand Pharma
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  Account Manager, Research & Safety Division - Thermo Fisher
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  Supply Chain Manager - mc2 therapeutics
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  Trial Start-up Manager specialised in start-up activities to prepare and improve our clinical trials - Novo Nordisk
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  Director Legal – Y-mAbs Therapeutical
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  Clinical Partnership & Vendor Manager - ALK
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  Channel Sales Manager - Flow Robotics
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  SAS Programmer - BioStata
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  Statistician - BioStata
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  Senior Regulatory Affairs Manager, CMC - Genmab
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  Senior Manager, Master Planner - Orphazyme
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  Global Head of QA - Orphazyme
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  Director of Quality Systems & Compliance - Orphazyme
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  Director of Quality Assurance Operations - Orphazyme
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  PostDoc, Computational Chemistry and Machine Learning - Zealand Pharma
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  Quality Assurance Manager, GMP - Genmab
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  Associated Director/Director of Global Clinical Drug Safety, Y-mAbs
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  Senior Scientist, Medicinal Chemistry - Zealand Pharma
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  Regulatory Manager – Thermo Fisher Scientific
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  HR Manager - Orphazyme