Regulatory Affairs Associate

Contract: 12 months (renewable)Employment: Outsourced through ManpowerGroupJob Purpose:The purpose of the Affiliate Regulatory Affairs role is to execute the operational aspects of regulatory affairs for the marketing affiliate, including:License maintenance activities (e.g. Labelling changes, CMC Changes, Renewals)New registrations, line extensions and new indications.Tracking regulatory procedures and archiving correspondence in accordance with local regulations and quality system requirements.Provide operational excellence to successfully achieve Affiliate regulatory objectives.Facilitate and cultivate relationships with relevant external regulatory personnelRegulatory Plan ExecutionCollaborate with the implementation of the Regulatory Plan in alignment with affiliate business plans as well as with regulatory requirements.Support submission of high quality regulatory applications within planned timelines.Support dossier preparation of new applications to obtain marketing authorizations.Coordinate administrative tasks (i.e. translations, legalizations, etc.) to facilitate dossier preparation.Execute maintenance activities for marketing authorisations (timely submission of post approval maintenance activities like renewals, variations and periodic reports).Support Dossier assembly in compliance with local regulations and quality system requirements.Maintain awareness of current regulations and upcoming changes in the regulatory environment. Communicate changes to appropriate management and cross-functional experts as appropriate and implement locally. Regulatory ComplianceKeep internal Regulatory IT tools up to date and accurateEnsure that all products comply with local regulations and quality system requirements whichever is more stringent.Keep the regulatory archive complete and up-to-date and ensure that all current licenses and labels are readily availableSupport implementation of local quality system in line with the global quality system and local regulations.Support internal audits / assessments / self-inspections in collaboration with Regulatory Quality personnel.Raise awareness on compliance issues with leadership and relevant functions.LabellingPerform the function of Primary, Delegate or Alternate Affiliate Labelling Responsible Person (ALRP), ensuring that Product Information complies with local regulatory requirements and that updated Product Information is submitted, approved and implemented within the designated internal and/or MOH timelines.Follow global labelling procedures and document relevant exceptions in order to produce accurate and high quality Product Information which is in compliance with global core labelingEnsure the effective execution of eLabeling and the maintenance of correct Product Information on the eLabeling website.Process ImprovementSupport implementation of relevant internal regulatory initiatives.Personal and Professional DevelopmentKnowledge and understanding of local regulations and local, regional and global regulatory procedures.If available, attend external regulatory training or MoH meetings focusing on local regulationsMinimum Qualification Requirements:Bachelor's degree in pharmacy or equivalent in a relevant scientific subjectGood communication skills.Demonstrated good computer/IT skills.Good knowledge of written and spoken English.Previous experience will be highly regardedOther Information/Additional Preferences:Ability to adapt to difficult and different challenges.Team working skills with special focus on results.Time management skills.Good capability to establish positive networking both internally and externally