Provide Quality Engineering skills for the Complaint Quality System and Process Improvements
Quality Engineering Complaint management and provide complaint trending analyses to support improvement of products manufactured in the facility. Maintain knowledge of product quality controls and failure modes. Evaluate complaint samples. Initiate and perform investigations, maintain & follow up on Quality Corrective Action Plans. Provide Progress Reports and trending to show product quality levels and respond to regulatory requests. Contribute to the continued adherence to regulations including cGMPs, GHTF & ISO standards. Support improvement efforts within the complaint handling process. May perform audits, support global complaint community initiatives, lead project/investigation teams and provide representation of the site's complaint investigations during internal or external audits. May perform other duties as requested by management
Posting Dates: 11/20/16 - 11/29/16
Work Schedule: 1st shift EEO Statement The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Minimum requirements B.S in Sciences and 2 years in QA cGMP manufacturing role that included investigations / CAPA
A little about us:
As the global leader in eye care, Alcon develops and manufactures innovative medicines and devices to serve the full life cycle of eye care needs.