position Regulartory Specialist
level 과장급
location 서울
compensation 협의가능
firm 외국계 Medical Device
summary
responsibilities -Prepare submissions for the new product registration -Perform regulatory assessments with relevant functions on international standards and Korea national deviations -Interface with local and global regulations to implement appropriate regulatory strategies - Develop and keep a good/strong relationship with the regulatory authorities, legislators and trade associations
requirements -Bachelor’s degree in Electronics Engineering / Biomedical Engineering -At least 3 years experience for product registrations & regulatory audits -Total Quality Management(TQM) administration experience -Good verbal and written English communication skills
status filled
posted on 2013-09-26
   

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