Empresa:

ALTEN Portugal

Descrição da Função

ALTEN Portugal, a leading force in the IT, Engineering and Life Sciences industries, is on the lookout for Junior Consultants 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?

Internship Overview

As a Junior Intern, you will support project teams within the areas of Commissioning, Qualification & Validation (CQV), Quality Assurance (QA), and Computer System Validation (CSV). This role offers valuable exposure to pharmaceutical industry standards and Good Manufacturing Practices (GMP), in a challenging and supportive environment.

You will contribute to regulated pharmaceutical projects involving system and equipment validation, documentation review, and compliance activities, under the guidance of senior consultants.

Profile Requirements:

• Recently completed a Master's degree in Pharmaceutical Sciences, Pharmaceutical Engineering, or Chemical Engineering
• Interest in working within GMP environments, particularly in CQV, QA, or CSV domains
• Strong motivation to learn and grow in the pharmaceutical consulting industry
• Good level of English (written and spoken)
• Eligible for an IEFP internship

What We Offer:

• 6-month internship (IEFP) in a recognized international consultancy
• Hands-on experience in real pharmaceutical industry projects
• Mentorship and support from experienced professionals
• Opportunity to develop core competencies in validation, QA, and regulatory compliance
• Collaborative, innovative, and inclusive work environment

Location: Lisbon, Portugal (100% on-site)

If you're looking to launch your career in the pharmaceutical industry and are passionate about quality and validation, we'd love to hear from you!

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.

Observações

Lisboa (Portugal)