Technician II, Quality in Carrigtohill at Stryker Corporation

发布日期: 9/15/2019

职位快速浏览

职位描述

Be a Subject Matter Expert with regard to Acceptable Quality Standards for products and processes.

Ensure Regulatory compliance in area to cGMP’s of all medical device regulatory agencies (e.g. FDA and TUV)

Represent QA as the first point of contact for daily line support issues.

Troubleshoot product and process related issues and identifies root cause.

Work with QE’s and product teams to identify areas for risk reduction and error proofing processes and work on implementation of these.

Drive Defect awareness training with product builders with the assistance of the manufacturing trainer.

MRB: Provide input into the disposition for any non-conforming product and identify appropriate corrective action with other support team members.

Perform internal quality audits.

Trending and analysis of key Quality metrics.

Responsible for the timely analysis of customer complaints to acceptable Quality Standards supporting Divisional and Operational goals and objectives.

Complete investigation and analysis of customer complaints.

Maintain systems for the receipt and recording of customer complaints

Assist in the preparation of periodic reports

All other duties as assigned.

Work From Home: No

Travel Percentage: None

欢迎加入人才网络

加入我们的人才网络可助力您的职位搜索和申请流程。无论您是选择申请职位还是只留下个人信息,我们都期待着与您保持联系。

加入我们的团队