Quality Assurance Officer

ALTEN Portugal, a leading force in the IT, Engineering and Life Sciences industries. We are currently seeking a dedicated and detail-oriented Qualification Assurance Technician 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.

Key Responsibilities:

• Know-how in GMP for Drug Products
• Management of Product Quality Complaints
• Document Control and Governance
• Change Control Management
• Non-Conformance Handling and CAPA Implementation
• Supplier Performance Monitoring
• Quality Records Maintenance

Qualifications:

• Bachelor's degree in Life Sciences, Engineering, or related field
• 2+ years of experience in Quality Assurance or Quality Systems
• Knowledge of GMP and regulatory requirements (e.g., FDA, EMA)
• Experience with product quality complaints, CAPA, and change control
• Familiarity with document control and QMS tools
• Strong analytical, organizational, and communication skills
• Proficient in data analysis for management review support
• Experience with supplier monitoring and quality record management
• Ability to work effectively in multidisciplinary teams and collaborate on technical reviews without direct leadership responsibilities.
• Familiarity with industry standards and regulatory requirements is highly valued.

Location: Hybrid, Vale de Cambra.

Why Join Us?

• Possibility to work with cutting-edge technology in the Life Sciences industry
• Collaborative and dynamic work environment
• Possibility to join a top-leading company in the industry
• Continuous trainings
• Possibility 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 and cover letter detailing your relevant experience and qualifications.