(Sr.) RA Specialist - ¿Ü±¹°èÁ¦¾àȸ»ç

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  • • Gather documents to assist with submission preparation dossier compilation in collaboration with senior RA team member.
     • Maintain proper records in the Module Change Request and JDE system to comply with local and company regulatory and quality requirements.
     • Assist in the gathering of information and research required by RA team.
     • Assist in the gathering of information and research used to provide guidance and feedback to team on registration requirements for new and renewal registrations, product and process changes.
     • Other incidental duties assigned by Leadership


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- Bachelor's Degree in related field, min 5 years experience previous related experience Required or
 - Other: in Scientific discipline (e.g., medical, pharma, Biology, Microbiology, Chemistry) Experience in preparing domestic and international product submissions Preferred
 - Other: Coursework, seminars, and/or other formal government and/or trade association training Preferred



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