Die Stelle Regulatory Affairs Manager (f/m/x) Medical Devices bietet folgende Benefits:
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We have revolutionized allergy diagnostics and have been operating successfully in more than 90 countries with our diagnostic products and patented technologies. Our products help clarifying allergies in a single step - for humans and animals alike. Allergies are diagnosed in a highly specific manner so that patients receive help by their specialist in no time. We increase quality of life, enable personalized treatment, advance research and relieve our health system.
Taking Ownership for the Post Market Surveillance System by establishing, maintaining, and continuously improving the Post-Market Surveillance (PMS) system in accordance with IVDR requirements (e.g., PMS plans, PMS reports, PSURs)
Set up and own a state-of-the-art Compliance Management System to ensure continued compliance with all relevant global standards
Preparing, reviewing, and maintaining SOPs, work instructions, and templates to ensure efficient and compliant regulatory processes
Acting as liaison to other departments with focus on collaboration with clinical on activities to ensure an up to date performance evaluation for all our devices
Support in preparing technical documents to support country-specific regulatory submissions of registration documents and maintaining, reviewing and updating regulatory submissions and documents
Evaluating regulatory impact for CAPAs, changes, and deviations, and providing strategic regulatory input
Assisting in responses to regulatory authorities, notified bodies and authorized representatives questions within assigned timelines
Supporting internal and external audits and inspections