Reliability & Methods Engineer

Job title: Reliability & Methods Engineer
Location: Framingham, MA

About the job

Role Purpose

The Reliability Engineer improves the reliability, maintainability, safety, and lifecycle performance of cGMP and non-cGMP manufacturing, utility, facility, and process systems.

Using asset-performance data, risk assessments, failure investigations, predictive technologies, and maintenance history, this role identifies systemic issues and implements sustainable improvements. The Reliability Engineer leads reliability investigations, preventive and predictive maintenance optimization, CAPAs, change controls, lifecycle planning, and reliability-centered improvements to single-use technology systems.

Department Description

The Site Maintenance & Reliability organization provides corrective and preventive maintenance, reliability engineering, calibration support, and technical services for site buildings, equipment, utilities, and manufacturing systems.

The organization is responsible for the reliable, efficient, and sustained operation of site assets while supporting manufacturing, project delivery, business objectives, and compliance with regulatory, quality, environmental, health, and safety requirements.

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you'll help reimagine how life-changing treatments reach people everywhere, faster.

About Sanofi:

We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.

Main Responsibilities

Key Responsibilities

Asset Performance and Risk Management

• Analyze CMMS/EAM data, downtime, deviations, work orders, maintenance costs, condition-monitoring results, spare-parts usage, and equipment history.
• Develop reliability dashboards, bad-actor lists, Pareto analyses, repeat-failure trends, and MTBF/MTTR reporting.
• Assess equipment criticality and risk using FMEA/FMECA, reliability-centered maintenance, safety, compliance, product impact, redundancy, obsolescence, and business-continuity considerations.
• Recommend risk mitigation, monitoring, acceptance, escalation, or asset replacement strategies.

Failure Investigation and Problem Solving

• Lead root-cause investigations for recurring, complex, high-impact, or poorly understood equipment failures.
• Evaluate failed components, alarms, operating conditions, maintenance history, design information, and human factors.
• Investigate emerging reliability concerns, including degrading performance, repeat work orders, nuisance alarms, abnormal condition-monitoring results, and increasing parts consumption.
• Develop sustainable corrective actions and verify their effectiveness.

Maintenance Strategy Optimization

• Develop and optimize preventive, predictive, and condition-based maintenance strategies.
• Select appropriate monitoring technologies based on equipment criticality, failure modes, technical feasibility, data quality, and cost.
• Define monitoring routes, frequencies, alarm limits, response workflows, training needs, and program performance measures.
• Use risk, failure history, condition data, and field feedback to add, revise, consolidate, convert, or retire maintenance tasks through approved governance processes.

Work-Order and Inventory Analysis

• Review corrective, preventive, predictive, and emergency work orders to identify repeat failures, maintenance-induced events, planning gaps, parts usage, and opportunities to improve job plans.
• Monitor critical spares, long-lead components, repairable assets, shelf-life exposure, obsolete inventory, and stockout risk.
• Recommend stocking levels and inventory strategies based on asset criticality, consumption, lead time, redundancy, and supplier availability.

Reliability Improvement and Lifecycle Planning

• Lead bad-actor elimination, equipment upgrades, system modifications, and replacement recommendations.
• Develop technical scopes, lifecycle cost evaluations, business cases, implementation plans, and effectiveness measures.
• Lead reliability-related CAPAs and change requests for systemic or longer-term improvements.
• Support the development and execution of reliability-related capital projects and system modifications.

Single-Use Technology

• Lead reliability-centered improvements to single-use technology assemblies and systems.
• Evaluate failure modes, component selection, connection interfaces, operating limits, installation practices, leak risk, supplier performance, usability, standardization, and maintainability.
• Coordinate approved changes with Manufacturing, Process Engineering, Quality, Validation, Procurement, and suppliers.

Engineering and Project Support

• Provide reliability requirements for new equipment, system modifications, capital projects, commissioning, qualification, and operational readiness.
• Define equipment criticality, maintenance strategies, predictive-monitoring requirements, spare-parts needs, acceptance criteria, documentation, and training requirements.
• Participate in design reviews to confirm reliability, maintainability, accessibility, redundancy, control strategy, safe-work, and lifecycle requirements.

Technical Leadership and Compliance

• Develop and maintain reliability standards, tools, templates, and analytical methods.
• Coach engineers, planners, mechanics, technicians, and system owners in reliability principles, investigation methods, and data-driven decision-making.
• Maintain accurate, traceable, current, and inspection-ready technical documentation.
• Perform work in accordance with cGMP, data-integrity requirements, Quality Systems, site procedures, HSE requirements, OSHA expectations, engineering standards, and approved change-control processes.
• Support planned shutdowns, utility outages, start-ups, system restoration, emergency conditions, and manufacturing escalations.

Decision Rights and Accountability

The Reliability Engineer:

• Selects appropriate reliability methods, data sources, analytical tools, and assumptions.
• Determines engineering risk ratings and recommends mitigation, monitoring, acceptance, or escalation through the applicable governance process.
• Defines the technical basis for predictive-maintenance technologies, monitoring routes, alarm limits, frequencies, and response strategies.
• Recommends evidence-based changes to preventive and predictive maintenance programs.
• Prioritizes bad actors and systemic reliability improvements based on safety, compliance, frequency, cost, and business impact.
• Is accountable for the quality and timely completion of assigned analyses, investigations, CAPAs, change requests, work-order reviews, inventory-risk assessments, and technical documentation.
• Escalates significant risks, repeat failures, overdue actions, and material cost, compliance, schedule, or manufacturing exposure.

Key Deliverables and Performance Measures

• Current asset-criticality and reliability-risk assessments with documented mitigation priorities.
• Routine reporting of bad actors, recurring failures, downtime drivers, and lifecycle cost opportunities.
• Timely root-cause investigations with sustainable corrective actions and demonstrated effectiveness.
• Effective predictive-maintenance programs with actionable alerts, route compliance, avoided failures, and measurable value.
• Reduced emergency work, repeat failures, and maintenance-related downtime.
• Improved preventive-maintenance effectiveness, job-plan quality, and labor utilization.
• Timely completion of reliability CAPAs, change requests, and work-order analysis actions.
• Reduced critical-spare stockout, excess-inventory, and obsolescence risk.
• Approved single-use technology improvements that reduce failure risk and improve standardization, usability, and maintainability.

About you

Basic Qualifications

• Bachelor's degree in mechanical, electrical, chemical, biomedical, or related engineering discipline, with at least 3 years of relevant engineering experience in manufacturing, facilities, utilities, laboratories, or complex process equipment in a regulated or high-reliability environment. Candidates without a bachelor's degree must have at least 8 years of such experience.
• Applied experience with reliability methods such as FMEA/FMECA, RCM, asset criticality, MTBF/MTTR, lifecycle costing, Pareto analysis, root-cause failure analysis, and maintenance-strategy optimization.
• Experience working in a regulated environment, including cGMP and applicable OSHA and environmental requirements.
• Experience analyzing CMMS/EAM, work-order, downtime, deviation, condition-monitoring, or inventory data.
• Experience leading equipment investigations, continuous-improvement initiatives, CAPAs, or change controls.
• Working knowledge of BMS, EMS, DCS, CMMS/EAM, data-visualization tools, and Microsoft Office applications.
• Strong technical writing, communication, facilitation, coaching, and cross-functional leadership skills.

Preferred Qualifications

• Experience in pharmaceutical or biotechnology manufacturing.
• Knowledge of manufacturing equipment, utility systems, process equipment, and single-use technologies.
• Experience implementing predictive-maintenance or condition-monitoring programs.
• Experience with commissioning, qualification, validation, and equipment lifecycle management.
• Familiarity with SAP, Maximo, Infor EAM, or comparable CMMS/EAM platforms.
• Experience with Lean, Six Sigma, statistical analysis, continuous improvement, or data visualization.
• CMRP, CRL, Lean/Six Sigma, project-management, Professional Engineer, or equivalent professional certification.

Key Working Relationships

• Site Maintenance & Reliability: Priorities, governance, resources, escalation, and performance commitments.
• Equipment Engineering and Maintenance: Technical ownership, failure findings, job plans, preventive-maintenance content, modifications, and execution.
• Manufacturing and System Owners: Operating context, equipment impact, access, performance trends, risk controls, and implementation.
• Quality, Validation, and Metrology: Deviations, CAPAs, change controls, impact assessments, qualification, calibration, and validated-state requirements.
• HSE and Automation: Safe operation, risk controls, alarms, control-system interfaces, data sources, and monitoring solutions.
• Procurement, Stores, and Suppliers: Inventory risk, repair strategies, obsolescence, supplier capability, lead times, and lifecycle support.

Working Conditions

• Ability to gown and access manufacturing areas.
• Ability to enter operating and maintenance areas to support troubleshooting, equipment inspections, and vendor activities.
• Participation in planned site shutdowns, utility outages, system start-ups, and restoration activities.
• On-call support may be required in accordance with site scheduling and escalation practices.

Why Choose Us?

• Bring the miracles of science to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
• Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.
• Power industry-leading performance by leveraging digital, data, and AI-driven innovation – at speed and scale.
• Transform lives worldwide by delivering life-changing treatments anywhere, anytime.

Sanofi US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

Sanofi US endeavours to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-866-SANOFI2 (1-866-726-6342) or click here

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

North America Applicants Only

The salary range for this position is:

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.