Analyze your CV for Executive - Regulatory Affairs at Shelys Pharmaceuticals Ltd

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About this job

Job DescriptionDesired ProfileEducation: Bachelor of PharmacyExperience: 0 – 4 yearsGood knowledge of Microsoft office and databasesReporting LineTo Head – Quality AssuranceDuties & responsibilities  Preparation of product registration dossiers for Tanzania and various other countries as per registration guidelinesReview of queries from regulatory agencies and ensure timely response to itTimely submissions of Amendments/Variations/annual updates, Technical Data Package/Open Parts of DMFs responses to regulatory agenciesTo maintain regulatory database, registrations, and compliance with proceduresSound knowledge on WHO, ICH, TFDA and other regulatory guidelinesResponsible for checking of artworks as per the guidelinesPreparation of technical file for tenders (Product Permission, CPPs, FSCs, Product License and other relates documents) as per business planAny other responsibilities given by the Head of the Department / ManagementInterested candidates have to send their application letters, updated CV (including three referees), copies of academic certificates and daytime telephone contact to the undersigned through the address and or email below.The Senior Human Resources ManagerShelys Pharmaceuticals LtdNew Bagamoyo Rd, MwengeP.O.Box 32781Dar es Salaaminfo@tz.betashelys.comImportant Note: Women and persons with disability are particularly encouraged to apply.Applications to reach us on or before 28.02.2018; only shortlisted candidates will be contacted.