Join the Japanese branch of Werfen, a global leader in IVD (in vitro diagnostics), as you engage in regulatory affairs and quality assurance for medical devices. Your role will have a focus on regulatory applications (70%) and quality assurance (30%). For RA, you will be responsible for product registration, preparation and submission of application documents, license registration, maintenance, health insurance, import-related tasks, and internal checks of promotional materials. For QA, your responsibilities will include documenting and revising management systems, acceptance testing, internal and external audit responses, and safety information reporting. With new products slated for market entry, you will leverage your expertise while collaborating with other departments and global teams.
The above information is a public job ad. This job ad is neither an offer nor a contract.
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