ALTEN Portugal
, a leading force in the IT, Engineering and Life Sciences industries. We are currently seeking a dedicated and detail-oriented
Quality Assurance technician
specialized in
quality assurance systems, processes and compliance.
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 technician
, you will play a critical role in
ensuring that products meet quality and safety standards, conducting inspections and tests throughout the production process, identifying and documenting defects, supporting continuous improvement initiatives, and maintaining compliance with regulatory and company requirements.
Key Responsibilities:
* Conduct inspections on raw materials, in-process products, and finished goods to ensure compliance with quality standards.
* Document and report quality issues, non-conformances, and test results accurately and promptly.
* Assist in root cause analysis and corrective/preventive action (CAPA) implementation to address quality deviations.
* Ensure compliance with company policies, regulatory requirements, and industry best practices.
* Prepare, organize, and maintain quality documentation and records, ensuring version control and accessibility.
* Participate in external and internal audit preparations, ensuring that all processes, documentation, and records are audit-ready and compliant.
* Manage and maintain the Quality Management System (QMS), ensuring documentation, processes, and records are up-to-date, compliant, and effectively implemented.
Qualifications:
* Bachelor's degree in Pharmacy, or Life Sciences related field.
* Minimum of 2 years of hands-on experience in Quality Assurance within the pharmaceutical industry (preferential).
* Strong knowledge and practical experience with Good Manufacturing Practices (GMP) and regulatory requirements.
* Proven ability to conduct inspections, manage quality documentation, and support audit preparations.
* Experience in root cause analysis and implementation of corrective and preventive actions (CAPA).
* Excellent organizational skills with a focus on maintaining version control and audit-ready documentation.
* Strong attention to detail and commitment to compliance with industry best practices and company policies.
* Effective communication and teamwork skills, with the ability to collaborate across departments.
Location:
Hybrid; Vale de Cambra, Aveiro.
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.