Senior Project Engineer
La risorsa opererà all’interno dei Servizi Tecnici con riporto diretto all’Engineering Manager, occupandosi della gestione ed implementazione di progetti complessi all’interno dello Stabilimento di Paullo.
Responsabilità
* Develop engineering activities to identify, evaluate and propose reliable technical solutions in compliance with Quality and Safety standards, both independently and in collaboration with external consultancy firms.
* Develop technical and economic feasibility studies for assigned projects.
* Ensure correct development and management of engineering documentation through all project phases.
* Collaborate with all company functions involved to define project requirements, ensuring correct translation into technical specifications and relevant documentation.
* Manage assigned projects, ensuring delivery timelines and defined budget, monitoring progress and managing deviations or corrective actions.
* Manage supplier relationships for RFx, evaluate offer compliance, and align them technically to support the Purchasing Office with commercial negotiations.
* Coordinate construction activities directly or with the support of available resources (internal and external specialists), ensuring conformity to defined technical specifications and Safety and Quality standards.
* Maintain constant communication and updates with internal stakeholders and clients regarding project progress, organizing regular alignment and review meetings.
* Ensure correct delivery of assigned projects, planning and following directly commissioning, testing and startup phases of plants.
* Guarantee that plants are ready for use and that technical documentation is properly managed and archived in accordance with company procedures.
Requisiti
* Laurea quinquennale in Ingegneria Chimica.
* At least 8–10 years of experience managing complex projects in Chemical/Pharmaceutical or engineering services environments.
* Solid technical foundations.
* Knowledge of HSE regulations (Machinery Directive, PED, ATEX Directive, safety legislative Code 81/08).
* Knowledge of quality regulations (EU/FDA cGMP, Guidelines, Standards).
* Knowledge of commissioning procedures (FAT/SAT) and plant commissioning management.
* Proficiency in MS Office, including project management tools such as MS Project or MS Visio.
* Intermediate knowledge and familiarity with Autodesk AutoCAD or similar software.
* Good command of English.
* Ability to work autonomously while maintaining teamwork, coordinating multidisciplinary project teams.
* Practical, results‑oriented approach.
* Organizational discipline in documentation management.
* Project Management, Teamwork and strong communication skills.
Preferenze
* Previous experience in designing and installing plants in specialized contract manufacturing organizations (CDMO) producing Active Pharmaceutical Ingredients.
* Experience working closely with maintenance departments.
* Experience in plant/utilities qualification activities in API production environments.
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