Sr. Equipment Process Engineer- Upstream
Sanofi
Summary
The Sr. 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.
Job description
About the Role
The Sr. 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.
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 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.
- Lead equipment changes and projects: define technical requirements and lead design reviews, vendor selection, FAT/SAT, commissioning, qualification, turnover, training, maintenance readiness, and documentation.
- Own technical quality actions: lead equipment-specific change controls and CAPAs, provide deviation assessments, and ensure approved hardware changes are implemented, tested, documented, and 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.
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.
- 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 Qualifications
- 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.
Requirements
- Bachelor's degree in mechanical, electrical, chemical, biomedical, or related engineering discipline
- 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
- 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
Benefits
- Health Insurance
- Prevention & Wellness Programs
- Career Development Opportunities
- International Career Mobility
- Competitive Rewards Package
Company overview
Sanofi is a French multinational pharmaceutical and healthcare company headquartered in Paris, France. Founded in 1973, the company has grown through strategic mergers and acquisitions to become one of the world's leading pharmaceutical corporations. Sanofi operates as an R&D-driven, AI-powered biopharma company committed to improving people's lives through breakthrough science. The company's portfolio spans seven major therapeutic areas including cardiovascular diseases, diabetes, oncology, immunology, rare diseases, neurology, and vaccines. Through its subsidiary Sanofi Pasteur, it is the world's largest producer of vaccines. Sanofi employs over 84,000 people across more than 100 countries and maintains a significant presence in both developed and emerging markets. The company's innovative pipeline focuses on advancing precision medicines and biologics while maintaining a strong commitment to sustainability and ethical business practices. Sanofi's mission centers on chasing the miracles of science to deliver transformative healthcare solutions globally.