Medical Device Regulatory Specialist

Il y a 7 heures

Flemish Brabant, Flanders, Belgique Michael Page Temps plein
pWat: /p pFrequentie: Dagelijks Wekelijks /p pOur client is an international healthcare organisation active in the medical device industry. The company develops and distributes products that support healthcare professionals and patient care across several international markets. /p pTo strengthen its Regulatory Affairs team, the organisation is looking for a Regulatory Affairs Specialist who will work closely with Quality, Clinical Affairs and other international stakeholders. /p h3Medical Device Regulatory Specialist /h3 pAs a Regulatory Affairs Specialist, Medical Devices your responsibilities are: /p ul liCoordinate medical device registrations across assigned international markets /li liPrepare, review and submit regulatory documentation with internal and external stakeholders /li liSupport regulatory compliance and manage changes throughout the product lifecycle /li liReview marketing materials and assess their regulatory implications /li liMonitor regulatory developments and communicate relevant updates internally /li liAct as a contact for manufacturers, distributors and competent authorities /li /ul h3Profiel /h3 pA successful 'Regulatory Affairs Specialist, Medical Devices' should have: /p ul liBachelor's or master's degree in Life Sciences, Biomedical Sciences, Pharmacy, Regulatory Affairs or a related field /li liBetween 1 and 3 years of Regulatory Affairs experience within medical devices /li liGood knowledge of MDR, product registrations and regulatory documentation /li liProactive and organised, with strong analytical and communication skills /li liComfortable working with international teams and different stakeholders /li /ul h3Aanbod /h3 pOur customer offers you: /p ul liA permanent contract with a competitive salary package /li liAttractive extra-legal benefits /li liInternational exposure within the medical device industry /li liStructured onboarding and development opportunities /li liThe possibility to build a long-term career in Regulatory Affairs /li /ul