招聘人数:若干
到岗时间:不限
年龄要求:不限
婚况要求:婚姻状况
1. Under limited supervision, perform responsibilities related to the Document Control and Change Control processes which support our diversified medical device product lines across multiple manufacturing facilities. This will include, but not limited to, the creation and maintenance of BOM, Item Masters, Documents, Change Orders and Quality System Documents.
2. Provide CTC project team support and guidance to make sure BOM, Item Masters, Documents, Change Orders and Quality System Documents are completeness and accuracy in accordance with CTC and GBU procedures.
3. Troubleshoot and resolve Agile problems for CTC,
4. Provide Agile Trainings to CTC.
5. Other tasks assigned by QMS manager
1. Has quality control knowledge
2. 5+ years working experience as document control, preferred in Medical Device industry.
3. Familiarity with various PC-Based viewing systems (WebView, Product View, Agile etc.). Proficient with Microsoft Office products (Word, Excel, Power Point, etc.).
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