ALTEN Portugal, a leading force in the IT, Engineering and Life Sciences industries, is on the lookout for a vibrant and driven Quality Assurance Officer to join our dynamic team in the Life Sciences division.
ALTEN Group Within 30 years, ALTEN has become leader in both outsourced Engineering and IT Enterprise Services. ALTEN, composed of 54,000 employees (88% engineers), carries out complex and highly technical projects throughout the value chain of 6,500 clients, the most prestigious companies in all sectors of industry, services and telecommunications. We work with key actors in the Aeronautics & Space, Defense & Naval, Security, Automotive, Rail, Energy, Life Sciences, Finance, Retail, Telecommunications and Services sectors.
Do you want to work in exciting projects at renowned clients? At ALTEN we believe that knowing and meeting the expectations of our consultants is a key factor in our success. Our consultants make the difference. Do you want to make the difference too?
As a Quality Assurance Officer, you will be responsible for managing and supporting key quality system processes, including product quality complaints, document control, change management, non-conformance and CAPA handling, supplier monitoring, and quality records maintenance. You will also contribute to data collection and analysis to support management reviews, ensuring compliance with regulatory standards and driving continuous improvement across the organization.
Key Responsibilities: Know-how in GDP for Drug ProductsManagement of Product Quality ComplaintsDocument Control and GovernanceChange Control ManagementNon-Conformance Handling and CAPA ImplementationSupplier Performance MonitoringQuality Records MaintenanceData Collection and Analysis for Management Review Qualifications: Bachelor's degree in Life Sciences, Engineering, or related field2+ years of experience in Quality Assurance or Quality SystemsKnowledge of GMP and regulatory requirements (e.g., FDA, EMA)Experience with product quality complaints, CAPA, and change controlFamiliarity with document control and QMS toolsStrong analytical, organizational, and communication skillsProficient in data analysis for management review supportExperience with supplier monitoring and quality record management Location: Lisbon, Portugal (Onsite)
Why Join Us? Possibility to work with cutting-edge technology in the Life Sciences industryCollaborative and dynamic work environmentPossibility to join a top-leading company in the industryContinuous trainingsPossibility to join different and interesting projects If you want to embrace in a new and challenging opportunity and are excited about the opportunity to contribute to our team, we want to hear from you! Please submit your resume detailing your relevant experience and qualifications.