
Industrial Maintenance & Reliability Engineer
- Loures, Lisboa
- Permanente
- Horário completo
- Develop and implement asset management strategies for critical equipment, including PMP, critical spare part identification, and optimization of spare part inventories. Ensure up-to-date and accurate equipment BOM;
- Lead troubleshooting efforts for equipment malfunctions; perform Root Cause Analysis (RCA) and implement effective Corrective and Preventive Actions (CAPA) to minimize downtime;
- Integrate and maintain maintenance activities within the Computerized Maintenance Management System (CMMS), preferably SAP PM, ensuring proper documentation and workflow alignment;
- Support drug product manufacturing operations, providing technical expertise to ensure equipment reliability in a GMP-regulated environment (experience in pharmaceutical or biotech operations is strongly preferred);
- Apply Reliability engineering methodologies, including RBI (Risk-Based Inspection), RCM (Reliability-Centered Maintenance), and SIL (Safety Integrity Level);
- Use data-driven decision-making to analyze equipment performance trends, conduct lifecycle assessments, and propose overhaul or replacement strategies for underperforming assets;
- Define, monitor, and continuously improve Key Performance Indicators (KPIs) for maintenance and reliability, aligned with operational excellence targets;
- Propose and implement innovative solutions to increase equipment performance, reduce maintenance burden, and support overall manufacturing efficiency;
- Apply condition-based maintenance (CBM) techniques, including vibration analysis, thermography, and Non-Destructive Testing (NDT) for piping and welding assessments;
- Ensure maintenance activities comply with local legislation, including DL 191/2019 and DL 50/2005 (Portugal-specific if applicable).
- Bachelor’s or Master’s Degree in Mechanical, Industrial, or Electrical Engineering (or related field);
- 3–7 years of experience in pharmaceutical or highly regulated manufacturing environments;
- Proficiency in SAP PM, CMMS systems, and Microsoft Office suite; experience with data visualization tools (e.g. Power BI) is a plus;
- Strong understanding of pharmaceutical regulatory requirements (e.g., FDA, EMA), validation processes, and documentation;
- Excellent communication and teamwork skills with the ability to collaborate across functions including Quality, Manufacturing, and Engineering;
- Certifications in maintenance or reliability (e.g., CMRP, Six Sigma, PMP) are a plus;
- Actively participate in internal and external audits, as well as regular client visits, representing the maintenance and reliability function and ensuring availability of technical documentation and compliance evidence;
- Fluency in Portuguese and English is mandatory, both written and spoken, to ensure effective communication in a global, regulated environment.