Reliability Engineer
Listed on 2026-08-22
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Engineering
Maintenance Technician / Mechanic, Quality Engineering, Process Engineer
Industry: Global Pharmaceutical Manufacturing
Company: EFOR
Duration: 12-month project (extension possible)
Employment Type: Full-time (W2) or C2C Contractor
About the OpportunityEFOR is seeking, for one of our major client, an experienced Reliability Engineer to support a large-scale Asset Reliability Optimization Program at a leading global pharmaceutical manufacturing site.
This role offers the opportunity to drive reliability improvements across manufacturing equipment, utilities, instrumentation, and facility systems by optimizing maintenance strategies, reducing recurring failures, and improving overall asset performance.
Key Responsibilities- Review and optimize preventive maintenance (PM) strategies, frequencies, job plans, and maintenance tasks.
- Analyze equipment failures, downtime, maintenance history, costs, and performance trends.
- Perform equipment criticality assessments and reliability risk evaluations.
- Lead or support Root Cause Analysis (RCA) using methodologies such as FMEA, 5 Whys, and Fishbone.
- Develop practical corrective actions to improve equipment reliability.
- Recommend optimized PM programs, spare parts strategies, and asset lifecycle improvements.
- Support CMMS data quality, maintenance master data, and preventive maintenance programs.
- Collaborate with Maintenance, Engineering, Operations, Quality, Calibration, and Instrumentation teams.
- Prepare reliability KPIs, technical recommendations, and progress reports.
- Experience in Reliability Engineering, Maintenance Engineering, Maintenance Optimization, or Asset Management.
- Experience with in pharmaceutical, biotech, vaccine, or other GMP-regulated manufacturing environments.
- Strong knowledge of preventive and corrective maintenance, reliability engineering, asset criticality, maintenance planning, and equipment performance analysis.
- Experience performing Root Cause Analysis (RCA), FMEA, 5 Whys, Fishbone, or similar methodologies.
- Familiarity with GMP documentation, Change Control, Deviations, and Data Integrity requirements.
- Experience with SAP PM, Maximo, Blue Mountain RAM, or other CMMS/EAM platforms.
- Knowledge of pharmaceutical manufacturing equipment, utilities, HVAC, instrumentation, automation, or facility infrastructure.
- Experience supporting maintenance optimization, asset lifecycle management, or spare parts optimization.
- Strong Excel skills;
Power BI is a plus.
Joining EFOR means working on high-impact Life Sciences projects for world-leading pharmaceutical companies while benefiting from a collaborative, entrepreneurial, and international environment. You'll contribute to critical manufacturing operations and help deliver reliability improvements that directly support operational excellence.
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