ALTEN Portugal, a leading force in the IT, Engineering and Life Sciences industries. We are currently seeking dedicated and detail‐oriented PFMEA Engineer Support with holistic process know‐how, experienced in developing, reviewing, and analysing PFMEA (Process Failure Mode and Effects Analysis) within regulated manufacturing environments.ALTEN GroupWithin 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?This role as a PFMEA Engineer Support requires a strong understanding of process design and factory operations, and the ability to work cross‐functionally to identify, assess, and mitigate process risks in compliance with GMP and Quality Risk Management principles.Key Responsibilities:Development and Comprehensive Management of PFMEAs- Create preliminary versions of PFMEAs based on existing technical information. - Oversee the entire process through to the final version, ensuring alignment with internal standards and best practices in the pharmaceutical industry.Facilitation of teams and technical meetings:- Lead meetings with multidisciplinary teams (production, quality, engineering, validation). - Gather input, validate failure modes, and ensure technical consensus.Identification and management of corrective actions:- Identify critical failure modes. - Create action plans, monitor implementation, and ensure closure within deadlines.Production of formal documentation:- Meeting minutes, attendance lists, drafts, and final versions of PFMEA. - Follow-up reports and associated engineering documentation.Compliance with norms and standards:- Work in accordance with internal standards and recognized PFMEA methodologies. - Ensure traceability, documentary accuracy, and alignment with regulatory requirements (GMP, audits, compliance).Qualifications:- Degree in Engineering (Chemical, Mechanical, Industrial, or similar) - Strong understanding of manufacturing processes, process design, and factory operations in regulated environments - Proven experience in developing, reviewing, and analysing PFMEA (Process Failure Mode and Effects Analysis) - Knowledge of GMP environments and regulated industries - Experience working cross‐functionally with Process Engineering, Production, Quality, Validation, and Maintenance teamsLocation: Lisbon (Hybrid)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 projectsIf 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.