Vaga de Quality Associate II

The Quality Assurance Associate II (QAA II) is responsible for the oversight and implementation of the Marken Quality Management System (QMS), Marken Standard Operating Procedures (SOPs), processes and policies required to manage and control Marken?s Storage, Distribution and Transportation, Kit Production Facility. The QAA II also need to ensure compliance with applicable regional and local regulations and requirements, and customer requirements as appropriate, but not limited to: current Good Manufacturing Practice (GMP), Good Distribution Practices (GDP), Good Storage Practices (GSP), ISO 13485 and .. Implement, communicate and maintain company?s quality systems at the facility, in compliance with Marken?s Global Quality Management System (QMS) requirements. Interact with clients on Quality Assurance (QA)/ GxP related matters. Effectively interact with Marken Departments and stakeholders to maintain that all QA tasks are appropriately supported by QA. Oversee an internal audit schedule and perform internal audits including report preparation and assessment and tracking of associated corrective and preventive actions (CAPA). Perform audits of external service providers as part of the vendor selection process. Tracking and overseeing all commitments for actions or changes made by Marken from previous audits. Host client audits and regulatory inspections, manage the audit report responses and act as Marken?s main representative, including and preparing of appropriate materials required within those audits when applicable. Manage issues and CAPA plans, collate CAPA metrics, and identify and implement quality improvement initiatives. Oversee activities that conclude on the appropriate close-out of all CAPA entries. Identify relevant GxP/ Quality related training needs and deliver or make they are deliver where required. Manage the change control. Ensuring that the Marken Quality System and GxP Program are implemented and maintained. Assisting in the evaluation of Marken-designated vendors and/or out-sourced activities. Ensuring the accuracy and quality of records and documents. Monitor that training for all personnel is conducted and documented. Coordinating and promptly performing any recall activity. Participate actively in all the internal Quality and/ or designated meetings. Keep informed of regulatory changes in Country/Region and prompt updates to SOPs as needed.