主な能力
職務責任
2. Collection and update of domestic/foreign medical device regulatory certifications and related regulations and standards.
3. ISO13485 and GMP quality system audit related matters.
4. Matters related to domestic/foreign medical device clinical trials.
理想的な求人
2. More than 10 years of experience in domestic and foreign medical factories or enterprises and as a quality control department supervisor
3. Be familiar with various quality system audits and quality project improvement countermeasure effect tracking, etc.
4. Familiar with domestic/foreign medical device regulatory certification and related regulations and standards
5. Familiar with process sheets, quality reports, etc.
6. Cooperate with business trips
その他条件
学科:無制限
経歴:職務経験8年以上
出張・出向:出張あり(年間累積時間未定)
会社の福利厚生