Description
nOur German client – family-owned company – attractive location in the South of Germany – specializes in developing, manufacturing, and marketing advanced medical devices, including innovative surgical technologies. With a global presence, they operate through their own affiliates and a network of distributors. The following vacancy needs to be filled as soon as possible:nn
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- nLead and support the registration and approval processes for all medical devices outside the EU.nn
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- nCollaborate effectively with distribution partners, service providers, and regulatory authorities.nn
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- nAssess international approval requirements, and prepare and review regulatory documentation with internal specialists.nn
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- nManage regulatory projects, ensuring timely adherence to deadlines and schedules.nn
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- nUniversity degree and initial professional experience in the field of international medical device approvalsnn
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- nGood understanding of technology and complex interrelationshipsnn
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- nInterest in working with international legal requirements and regulationsnn
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- nGood problem-solving and communication skillsnn
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- nIntercultural competence and very good command of spoken and written Englishnn
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- nFlexible working hoursnn
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- nInduction programme and on-demand trainingnn
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- nFamily-friendly work environmentnn
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- nOccupational health and safety managementnn
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- nOccupational pension plannn
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- nSecure job in a modern companynn
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