Requirements
Bachelor’s degree in Pharmacy, Chemistry, or a related field.Minimum 10 years of experience in Quality Assurance within the pharmaceutical industry with Strong understanding of cGMP, regulatory compliance, and quality management principles and expertise in validation activities for both sterile and non-sterile operations.Experience in managing teams and leading audits, strong experience in managing diverse customer requirements, technology transfer projects, and setting timely communication with customers.Excellent English, analytical, problem-solving, and communication skills.Proven ability to lead diverse teams across multiple geographical regions.Solid background in new product project management, technology transfer, and product launches in compliance with EU standards.
Description
Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.Job Summary:We are seeking a passionate and talented Quality Assurance Section Head to join our dynamic team. The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry. Key Responsibilities:Lead the Quality Assurance department to ensure compliance with regulatory standards and the implementation of quality management systems.Develop, review, and approve quality policies, procedures, and specifications, as well as monitor their implementation to ensure adherence to cGMP and other applicable guidelines.Conduct audits and assessments of manufacturing processes, quality systems, and documentation to ensure compliance and identify areas for improvement.Manage and coordinate CAPA (Corrective and Preventive Action) processes, ensuring timely and effective resolutions to quality issues.Lead team training initiatives to enhance staff understanding of quality assurance practices, cGMP, and regulatory requirements.