SPECIALIST REGULATORY COMPLIANCE EMEA (M/W/D)

Abbott Medical is looking for a Specialist Regulatory Compliance EMEA (m/w/d) based in Eschborn near Frankfurt/ Main or other Abbott Medical sites in Europe PURPOSE OF THE JOB The Specialist Regulatory Compliance supports EMEA across the cardiovascular und neuromodulation divisions to comply with regulatory requirements of the MDD, MDR, national legislation in EU and non-EU countries, Switzerland, United Kingdom, Middle East and Africa.
ROLES & RESPONSIBILITIES Support EMEA countries in understanding and knowledge of the medical device legislation (MDD, MDR, national legislation in EU and non-EU countries, Switzerland, United Kingdom, Middle East and Africa) Support countries in the relationship to Competent Authorities, e.
.
support Competent Authorities requests for Vigilance Reports or Field Actions.
Support countries in Post-Market Surveillance activities, e.
.
Product Experience Reporting, Field action coordination and execution.
Support Stop Shipments in EMEA countries.
Create Training Material and conduct training as appropriate Create and generate reports, as required for FSCAs and monthly regulatory reports to monitor regulatory compliance.
Support Quality Audits in the countries.
Support EU and CH Authorized Representative and the Person Responsible for Regulatory Compliance.
Support Verification activities as required for Economic Operators according to the MDR and the CH MedDo.
Support MDR and CH MedDo projects, e.
.
Eudamed, Swissmedic Data Base Support Tender upon request from Regulatory Affairs EMEA EDUCATION & COMPETENCIES Knowledge and experience in medical device legislation (MDD, MDR, national legislation) Knowledge and experience in post market surveillance Experience in cooperation with Competent Authorities Technical, natural science, medical background or adequate experience Able to cooperate with local teams as well as with the US based manufacturer Familiar with Microsoft Office and willingness to work with other databases Willingness to meet documentation and follow-up obligations in all areas.
Fluent in English ABOUT ABBOTT \u00A0 Abbott is a global health care leader, creating breakthrough science to improve people\us health.
\u00A0 We\ure always looking towards the future, anticipating changes in medical science and technology.
u00A0 \u00A0 \u00A0 W ORKING AT ABBOTT \u00A0 \u00A0 At Abbott, you can do work that matters and help people to live a healthier and full life, grow your career, and learn, be your true self.
You will have access to.
u00A0 \u00A0 Career development with an international company where you can grow the career you dream \u00A0 of \u00A0 An attractive benefits package A company r ecognized as a great place to work in dozens of countries around the world \u00A0 and \u00A0 named one of the most admired companies in the world by Fortune.
u00A0 \u00A0 A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
u00A0 \u00A0 A challenging position in a fast-growing crisis independent industry To become part of a dynamic, highly educated, highly skilled, and motivated team Flat hierarchies, open appreciative mentality, and efficient, constructive lines of communication Multi-national environment, where we foster the development of our talents within the enterprise \u00A0 Follow your career aspirations to Abbott for diverse opportunities with a company that \u00A0 can help you \u00A0 build your future \u00A0 and live your best life.
Abbott is an Equal Opportunity Employer, committed to employee diversity.
\u00A0 \u00A0 We ask for \u00A0 your \u00A0 understanding that we only consider online applications via our online application portal.
Applications by email or post cannot be processed.
Original documents will not be returned.
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