Senior Equipment Process Engineer- Upstream

Sanofi; Framingham (MA); On-site; USD 120,000 - 170,000; Full time

Benefits offered by this job

Healthcare benefits

Parental leave (14 weeks)

Job summary

Sanofi Group in Framingham, MA is seeking a Senior Equipment Process Engineer- Upstream to own and optimize equipment lifecycle, lead troubleshooting, and drive maintenance strategies. The role combines hands-on field work with cross-functional leadership to improve safety, compliance, and reliability across manufacturing assets.

You will develop maintenance work packages, coordinate with operations, quality, validation, and engineering teams, and guide modifications and turnover for new

Qualifications

• Demonstrated equipment troubleshooting capability using drawings, manuals, data, failure history and root-cause methods.
• Experience developing job plans, PM tasks, technical specs, spare-parts recommendations, or maintenance strategies.
• Experience supporting equipment modifications, commissioning, qualification, change control, deviations, or CAPAs.

Responsibilities

• Own equipment performance and lifecycle including asset health and maintenance strategy.
• Lead troubleshooting and field support, working with mechanics and technicians.
• Develop and approve complete maintenance work packages with safety and testing criteria.
• Drive reliability improvements using data to reduce downtime and failures.
• Coordinate with vendors and cross-functional teams for projects and changes.

Education

Bachelor's degree in mechanical, electrical, chemical, biomedical, or related engineering discipline

Tools

CMMS/EAM systems

P&IDs and electrical diagrams

Instrumentation packages

Job description

Senior Equipment Process Engineer- Upstream# Sanofi Careers## Senior Equipment Process Engineer- UpstreamApply: Framingham, MA: Full time: Posted Yesterday: End Date: January 5, 2027 (30+ days left to apply): R2877269**Job Title**: Senior Equipment Process Engineer- Upstream * Location: Framingham, MA**About the Job** The Senior Equipment Process Engineer- Upstream is the technical owner for an assigned portfolio of manufacturing, utility, facility, or laboratory equipment. This role improves equipment safety, compliance, availability, and lifecycle performance by combining hands-on troubleshooting with effective maintenance strategies, equipment changes, technical documentation, and cross-functional leadership. 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 lives.**Main Responsibilities** * **Own equipment performance and lifecycle:** Maintain asset health, design basis, operating limits, criticality, failure history, documentation, maintenance strategy, obsolescence risks, and improvement priorities.* **Lead troubleshooting and field support:** Diagnose complex mechanical, electrical, instrumentation, and control-interface issues. Partner directly with mechanics and technicians through repair, testing, and return to service.* **Build executable maintenance plans:** Develop and technically approve complete work packages, including scope, sequence, labor, parts, tools, permits, LOTO, acceptance criteria, post-maintenance testing, and restoration requirements.* **Optimize preventive maintenance and spares:** Create risk-based PM strategies, equipment BOMs, critical-spares lists, stocking recommendations, and obsolescence mitigation plans using equipment criticality, failure modes, OEM guidance, and operating history.* **Lead equipment changes and projects:** Define technical requirements and lead design reviews, vendor selection, FAT/SAT, commissioning, qualification, turnover, training, maintenance readiness, and documentation for modifications and new equipment.* **Own technical quality actions:** Lead equipment-specific change controls and CAPAs, provide timely deviation assessments, and ensure approved hardware changes are implemented, tested, documented, and effectively closed.* **Drive reliability improvement:** Use downtime, repeat work, deviations, maintenance findings, and condition data to eliminate bad actors and improve reliability, maintainability, safety, and compliance.* **Coordinate vendors and stakeholders:** Develop technical scopes, assess vendor capability and performance, and collaborate with Operations, Quality, Validation, Metrology, HSE, Automation, Engineering, Procurement, Stores, and Finance.**Key Deliverables** * Technically complete, schedule-ready work packages and maintenance master data.* Risk-based PM programs, accurate equipment BOMs, and critical-spares strategies.* Timely, technically sound closure of deviations, CAPAs, change controls, and engineering actions.* Reduced repeat failures, emergency work, avoidable downtime, and obsolete-component exposure.* Complete maintenance readiness and technical turnover for equipment changes and new assets.* Accurate, traceable, and inspection-ready drawings, specifications, manuals, and records.**About You****Basic Qualifications** * Bachelor's degree in mechanical, electrical, chemical, biomedical, or related engineering discipline.* At least 3 years of engineering experience supporting manufacturing, facilities, utilities, laboratories, or complex process equipment in a regulated or high-reliability environment.* Demonstrated equipment troubleshooting capability using drawings, manuals, data, failure history, and structured root-cause methods.* Experience developing job plans, PM tasks, technical specifications, spare-parts recommendations, or maintenance strategies.* Experience supporting equipment modifications, commissioning, qualification, change control, deviations, or CAPAs.* Ability to work effectively in the field and communicate technical risk and recommendations to technical teams and leaders.**Preferred** * Experience in biopharmaceutical, pharmaceutical, medical-device, SUT, or other cGMP manufacturing.* Working knowledge of CMMS/EAM systems, equipment BOMs, work-order controls, and maintenance master data.* Knowledge of reliability methods, including criticality, FMEA, root cause analysis, condition monitoring, bad-actor elimination, and lifecycle planning.* Experience with P&IDs, electrical and mechanical drawings, instrumentation, controls interfaces, and OEM technical packages.* PE, CMRP/CRL, Lean/Six Sigma, project-management training, or related professional certification.**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 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.