Junior Q&V Engineer Porto

Junior Q&V Engineer
Porto
Porto, Porto District, Portugal

ALTEN Portugal
, a leading force in the IT, Engineering and Life Sciences industries. We are currently seeking a dedicated and
- oriented
Junior Q&V Engineer.

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
Junior Q&V Engineer
, you will support the execution of validation activities, ensuring compliance with industry standards, regulatory guidelines, and company quality systems. You will work alongside experienced engineers on projects involving equipment qualification, process validation, and continuous improvement initiatives.

Key Responsibilities:

• Assist in preparing and executing validation protocols (IQ, OQ, PQ) for pharmaceutical equipment and systems.
• Support risk assessments, data analysis, and technical documentation in line with GMP and regulatory requirements.
• Collaborate with
  - functional teams (Engineering, Manufacturing, Quality Assurance) to ensure successful project delivery.
• Troubleshoot equipment and process issues, providing technical input for resolution.
• Maintain accurate records, reports, and documentation to ensure compliance.
• Contribute to process improvements and efficiency initiatives.

Qualifications:

• Degree in
  Mechanical Engineering
  , Biomedical Engineering, Chemical Engineering, or a related technical discipline.
• 0–2 years' experience in validation, quality, or engineering within the pharmaceutical / medical device / biotech sector (internships and placements considered).
• Strong technical writing and documentation skills.
• Knowledge of GMP, FDA, and EU regulatory requirements (advantageous but not essential; training provided).
• Problem-solving mindset with attention to detail.
• Excellent communication and teamwork skills.

Location:
Porto, Portugal (Onsite).

Why Join Us?

• Possibility to work with
  - edge technology in the Life Sciences industry
• Collaborative and dynamic work environment
• Possibility to join a
  - 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.