Regulatory afairs associate
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Self-motivated Regulatory Affairs Associate holding 2.5 years of pharmaceutical industry work experience. Excellent project management abilities, including facilitation, organization and time management. Talented at providing regulatory leadership for new product development and change management activities. Highly successful at keeping on top of changes in requirements to maintain flawless compliance, and looking for a challenging new role. During my time in regulatory affairs, I have created dossiers for human pharmaceuticals, medical, and IVD medical devices, at times being the forefront of creating new procedures and workarounds for challenging submissions or during software crises. I pride myself on being a quick, conscientious learner; eager for learn something new while also continuing to develop skills I have already.
3 years experience in regulatory affairs - experience in medical devices, IVD, and Pharmaceutical drugs. Experience in whole of EU, America, Canada, and Switzerland.
Experience in leading teams, coordinating and working with different departments to meet deadlines. Being in charge o country portfolios and leading meetings to discuss work projections
Bachelors in biology masters in microbiology
