Quality Assurance Supervisor | Palhoça-SC

Important global chemical industry seeks a Quality Assurance Supervisor to lead and supervise activities related to the quality management system. The position will be responsible for ensuring compliance with internal standards, regulatory requirements, and good practices, as well as monitoring audits, document management, suppliers, non-conformities, and improvement plans. We are looking for an analytical, organized profile with leadership capacity and a focus on continuous improvement, who has experience in industrial environments and a strong orientation toward quality and compliance.

Responsibilities and assignments Implement and maintain Good Fractionation and Distribution Practices for Pharmaceutical Inputs (BPFD), providing tools for the monitoring and control of all processes and seeking constant process improvement Lead internal quality audit activities to certify process adequacy and evaluate compliance with regulatory standards Manage compliance with the Equipment Qualification and Calibration Schedule, including evaluation of the technical team and review of received reports with correct disposition Responsible for managing internal and external quality deviations, such as complaints, returns, and audit non-conformities Responsible for document control of the quality management system Represent the company before representative associations, participating in meetings and technical discussion forums, involving related areas when necessary and disseminating pertinent information internally Responsible for managing the qualification of national and international suppliers Supervise the improvement of the ANVISA Regulatory Framework, as defined in the Regulatory Agenda, preparing reports and bulletins sharing information and understandings of legislations and their impacts with the pertinent areas Define and manage area indicators, monitoring and proposing process improvement actions aiming to meet area/company goals Supervise the activities of the quality assurance team, ensuring that procedures and policies are followed.

Requirements and qualifications People Management: Lead the team to achieve area and business goals Negotiation Negotiate: actions and deadlines with areas Conflict management: Manage conflicts in the best possible way Project management: Perform management of improvement projects Verbal and written communication • Minimum of 5 years of experience • Completed degree in Farmácia; • Active CRF; • Desirable course/post-graduation in Quality Assurance in the Pharmaceutical Industry; • Experience in the Quality Assurance segment in the pharmaceutical, food, and industrial sectors; • Experience in People and process management. • Solid knowledge of current legislations and technical standards (national and international); • Office Package – Intermediate/advanced level • English – Advanced • Spanish desirable • Solid knowledge of quality tools