关键能力
工作职责
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.
理想人选
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
其他条件
科系:不拘
年資:8年以上工作经验
出差外派:需出差,一年累积时间未定
公司福利