Our client, a leading manufacturing company currently have a requirement for a Quality Engineer based in the Midlands.
Duties/Responsibilities:
Co-ordinate the execution of the site FDA-readiness action plan(s) via project-management leadership and interaction with all functional areas.
Assist in identification of process / system improvements across the site, develop and execute plans to address same.
Provide Quality Engineering support (problem solving, trouble shooting, FMEA, improvement initiatives) to all functions across the site.
Provide quality leadership to key site initiatives e.g. 5S, Near Miss Program, CIPs etc.
Lead problem solving and driving continuous improvements by analysis of quality data.
Support all areas in identification and implementation of effective CAPAs.
Support FDA-readiness training and awareness activities.
Liaise with area owners to identify Quality system risks and co-ordinate improvement plans.
Demonstrate an understanding of the application of the Quality Policy through daily activities.
Maintain vigilance to ensure adherence to the Quality Policy and system procedures by promptly reporting noncompliance issues to management.
Bring potential product / process Quality issues to the attention of Quality Management.
Conduct business in a manner that will protect human health, safety and the environment by complying with all applicable EHS laws, as well as the company's Global & Technical Standards
Requirements
Biomedical/Scientific/Quality/Engineering discipline with 2 years in Quality, Technical, Regulatory or Manufacturing areas within the pharmaceutical or devices industry
To apply for this position please send your CV to xxxxxx@xxxxxxxxxxxxxxxxx.xx
Please note: Your CV will not be put forward to the company without your prior permission.
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