Empresa:

ALTEN Portugal

Descrição da Função

ALTEN Portugal, a leading force in the IT, Engineering and Life Sciences industries, is on the lookout for a vibrant and driven Mechanical Engineer to join our dynamic team.

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 Mechanical Engineer with a strong background in piping systems, utilities, and mechanical infrastructure projects within GMP-regulated environments.

This role requires solid technical knowledge in mechanical and utility systems, familiarity with regulatory compliance and the ability to translate complex engineering requirements into effective technical solutions.

Key Responsibilities:

Guideline Development:

• Participate in the planning, execution, and supervision of piping installation and modification projects (utilities, process lines, HVAC systems, etc.).
• Design, specify and select mechanical components and piping materials in accordance with GMP and project requirements.
• Perform technical evaluations and ensure compliance with relevant industry standards, guidelines, and safety regulations.
• Review and approve mechanical engineering documentation such as P&IDs, isometrics, equipment datasheets, and layout drawings.
• Collaborate with multidisciplinary teams (automation, electrical, validation, production) to ensure mechanical systems meet process needs.
• Support commissioning and qualification activities for new or modified mechanical systems.
• Coordinate preventive and corrective maintenance activities for mechanical installations and utilities (e.g., WFI systems, steam, compressed air, chilled water).
• Troubleshoot mechanical issues in equipment, piping, or utilities and implement technical solutions to ensure minimal production downtime.
• Ensure the reliability, integrity, and continuous improvement of critical mechanical assets.
• Prepare and maintain technical reports, maintenance logs, and work procedures in compliance with GMP documentation practices.
• Ensure that all activities are conducted in compliance with GMP, health & safety, and environmental regulations.

Experience & Qualifications:

Education:

• Bachelor's or Master's degree in Mechanical Engineering or a related field.

Experience:

• Minimum of 2 years of experience in mechanical engineering roles, preferably in the pharmaceutical or life sciences industry.
• Experience in piping design, specification, and installation for utility and process systems (e.g., WFI, clean steam, compressed air, HVAC, etc.).
• Previous involvement in equipment installation, commissioning, and qualification within GMP-regulated environments.
• Experience in reviewing and interpreting technical drawings (P&IDs, isometrics, general arrangements).
• Familiarity with managing or supporting multidisciplinary engineering projects.

Technical Skills:

• Solid understanding of mechanical systems, piping layout design, and construction methodologies.
• Knowledge of applicable mechanical codes and standards (e.g., ASME BPE, ISO, EN standards).
• Ability to use engineering software/tools for piping and mechanical design (e.g., AutoCAD, Plant 3D, SolidWorks).
• Strong analytical and troubleshooting skills related to mechanical installations.

Nice to Have:

• Familiarity with GMP requirements and engineering documentation in the pharmaceutical industry.
• Knowledge of qualification and validation processes (IQ/OQ) related to mechanical systems.
• Experience working in cleanroom or controlled environments.

Location: Loures, Lisboa, Portugal (100% on-site)

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 detailing your relevant experience and qualifications.

Observações

Lisboa (Portugal)