ALTEN Portugal
, a leading force in the IT, Engineering and Life Sciences industries. We are currently seeking a dedicated and detail-oriented
Qualification and Validation Enginee
r with hands-on experience in
executing IQ/PQ protocols, reviewing and approving technical documentation
, and ensuring
equipment and process compliance within GMP-regulated environments.
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
Qualification and Validation Engineer
, you will play a critical role in
monitoring and reviewing equipment qualification and validation activities
,
ensuring full compliance with IOPQ protocols
, technical specifications, regulatory standards, and applicable
GMP legislation
.
Key Responsibilities:
* Support the equipment supplier in the external IOPQ protocol and approve the documentation
* Perform and execute internal IOPQ protocol
* Create and update internal documentation,
such as SOP's, Master lists, reports, assessment reports and others
* Perform calibration tests:
temperature, pressure, speed, conductivity and others
* Perform validation tests:
HDS, HPS, Mappings, Smoke tests, Environmental Tests, Distribution Studies and others
Qualifications:
* Bachelor's degree
in Engineering, Pharmaceutical Engineering, Industrial Engineering, or a related technical field.
* Minimum of 1–2 years of experience in equipment qualification, validation activities, or GMP-regulated engineering projects
, including reviewing technical documentation and supporting IOPQ execution.
* Strong analytical and problem-solving skills,
with attention to technical details and documentation accuracy.
* 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: Sintra,
Lisbon (Portugal)
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.