Empresa:

ALTEN Portugal

Descrição da Função

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

We are seeking a highly motivated Project Engineer to join our dynamic team, supporting the design, implementation, and optimization of pharmaceutical manufacturing facilities and systems. You will play a key role in developing engineering solutions, ensuring GMP compliance, and driving continuous improvement in facility performance.

Key Responsibilities:

• Lead the planning and enhancement of manufacturing plants and associated infrastructure for optimal functionality and efficiency.
• Develop and validate User Requirement Specifications (URS) to ensure installations are aligned with ergonomic and operational goals.
• Deliver innovative engineering strategies to support both new project developments and ongoing operations.
• Coordinate procurement efforts, including vendor selection, bid comparisons, and order processing.
• Generate and evaluate technical documentation throughout all project phases-from early concepts to detailed engineering.
• Monitor and control project scope, timelines, and financials to ensure successful and cost-effective execution.
• Supervise the delivery phases of projects, including construction oversight, systems integration, equipment startup, and validation.
• Collaborate closely with internal departments and third-party engineering firms to harmonize multi-disciplinary inputs.
• Promote adoption of emerging technologies and methods to improve performance and operational workflows.
• Uphold compliance with cGMP standards, corporate procedures, and EHS (Environmental, Health & Safety) policies.
• Assist with inspection readiness, staff training, and generation of technical reports and decisions.
• Report to senior management on project progress, emerging challenges, and risk mitigation strategies.

Qualifications:

• Degree in Engineering (Mechanical, Process, Chemical, or related discipline).
• Proven experience in pharmaceutical, biotechnology, or regulated manufacturing environments.
• Strong knowledge of GMP, validation, and commissioning practices.
• Excellent communication and project management skills.
• Ability to manage multiple priorities and collaborate across multidisciplinary teams

Location: Seixal, Portugal (Onsite).

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.

Observações

Setúbal (Portugal)