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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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À̸ÞÀÏ: carly.lee@peoplework.co.kr******@*******.***
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