Reliability & Methods Engineer: GMP-Driven Precision

Sanofi Group; Swiftwater (Monroe County); Presencial; USD 86.000 - 124.000; Tempo integral

Resumo da vaga

Sanofi is seeking a Reliability & Methods Engineer to lead reliability strategies for production equipment at the Swiftwater site and drive RCA/RCM driven maintenance improvements. The role focuses on optimizing maintenance programs, reducing downtime, and enhancing overall equipment effectiveness (OEE) within a GMP framework.

You will leverage SAP PM/EAM data, collaborate with Manufacturing, Quality, Validation, and Engineering, and ensure changes are GMP‑compliant and well-documented.

Qualificações

• Bachelor's degree required.
• Proven experience with reliability engineering methodologies (RCA, RCM, FMEA, failure analysis, OEE).
• Experience with SAP PM/EAM and maintenance data analysis.
• Knowledge of pharmaceutical manufacturing processes and GMP standards.
• Ability to read and interpret mechanical drawings, P&IDs, electrical schematics, and PLC/HMI docs.

Responsabilidades

• Develop, implement, and improve reliability strategies (RCA, FMEA, RCM).
• Lead root cause analysis for equipment failures and deviations and track CAPAs.
• Optimize preventive and predictive maintenance in SAP to improve MTBF, MTTR, and OEE.
• Collaborate with Maintenance, Manufacturing, Quality, Validation, and Engineering on changes and qualification activities.
• Manage vendor relationships, spare parts strategy, and capital project support.

Conhecimentos

RCA

RCM

FMEA

OEE

SAP PM/EAM

GMP knowledge

Documentation skills

Cross-functional collaboration

Formação

Bachelor's degree

Descrição da vaga

Sanofi is seeking a Reliability & Methods Engineer to lead reliability strategies for production equipment at the Swiftwater site and drive RCA/RCM driven maintenance improvements. The role focuses on optimizing maintenance programs, reducing downtime, and enhancing overall equipment effectiveness (OEE) within a GMP framework.

You will leverage SAP PM/EAM data, collaborate with Manufacturing, Quality, Validation, and Engineering, and ensure changes are GMP‑compliant and well-documented.