Your scope of work:Regulatory Information & Management System RIMs:Manage Affiliate regulatory activities on relevant Roche systems : RIMs, SERT, GPRS-PID, IP, CRDB.Ensure RIM system compliance with regards to dates tracking, archival and content management.Manage product information updates with respect to Roche and local regulatory requirements and for Roche databasesEnsure that complete records/files of all product dossiers and updates submitted and approved by the regulatory authorities are maintained and archived properly on RIM and internal databases.Other :Support on life-cycle maintenance/updating of registered products for any changes/updates other registration activities as required.Coordinate cross-functional collaboration with Marketing associates on promotional material submission processes. Serve as a key liaison between Regulatory partners, Marketing Associates , and Finance departments to facilitate smooth regulatory interactions.Any other duties that may be assigned from time to time as required by the business.Ensure timely preparation, submission of regulatory dossiers and related documentations: New Marketing authorization,variations and renewals to the local HA.Who you are:You have a Degree in PharmacyYour have Knowledge in pharmaceutical regulations and local requirementsYou have tenacious attention to detail and consistency, especially with respect to data, style, format, and layout and ability to format technical documents using electronic toolsYou have the skills for collaboration and the ability to interface effectively with colleagues You have ability to work in fast-paced teamsYou have logical thinking and/or process analyst mentalityYou are fluent in English & French
Secteur d'activité:
Services
Type de poste:
CDD Ou Mission
Niveau d'études:
Doctorat
Années d'experience:
Débutant / Junior
Catégories:
Santé, Médical, Pharmacie
Publiée le:
29-06-2025 à 12:24:14
