Role DescriptionThe Quality Specialist will be focused on managing the Complaint Handling and Corrective Action Preventive Action (CAPA) processes. This position requires the ability to drive improvement across multiple functional areas and locations. The Quality Specialist must be a good problem solver and relentless in ensuring the root cause of the problem is addressed. Good judgment skills are necessary to ensure the appropriate balance of quality, compliance, and business needs.
Responsibilities- Release/Rejection of the batches - Investigate complaints - Drawing, analyze and track CAPA's, reporting to clients if required - Performing internal audits - Plan and execute quality control activities - Suggest process improvements - Facility while ensuring compliance with all existing GMP and safety standards in the area of responsibility - Analyze change requests, review the class of change, determine the impact on the organization - Drafting and updating of quality agreements with customers and suppliers
Requirements- Master's degree or equivalent experience - A minimum of 3-5 years of experience in Quality in the pharmaceutical industry - Knowledge of GMP - Accuracy, tidiness, teamwork, eye for detail
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Windimi Post.
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