Reliability Engineer
Syner-G
August 26, 2026
Full-time
On-site
Boston, MA
Operations
Role: Reliability Engineer supporting GMP-regulated pharmaceutical or biotech manufacturing facilities by enhancing equipment reliability and optimizing maintenance strategies. Responsibilities include developing preventive maintenance programs, conducting equipment criticality assessments, leading root cause analyses, analyzing performance data, and improving asset management processes. Requires collaboration across Facilities, Engineering, Maintenance, Manufacturing, and Quality teams to ensure operational readiness and reduce unplanned downtime. Qualifications: Bachelor's in Chemical, Mechanical, Electrical, or related engineering discipline; minimum 1 year of relevant experience, preferably within biotech, pharma, or R&D settings; experience with reliability engineering principles, CMMS platforms (e.g., Maximo, SAP), and data analysis; knowledge of GMP and GEP standards. Preferred: hands-on support for GMP utilities, process equipment, or new asset commissioning; familiarity with RCM, FMEA, predictive maintenance, and condition-based strategies; experience supporting equipment validation and qualification. High-Value: focus on equipment reliability within regulated biopharma manufacturing, supporting continuous improvement initiatives, and ensuring operational compliance. Work Setup: travel up to 100% to client sites; primarily on-site in regulated environments.