Technician II, Quality de Carrigtohill em Stryker Corporation

Data de Postagem: 9/15/2019

Resumo do Emprego

Descrição do Emprego

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

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