Device Quality Engineer - Device Risk Management and Surveillance Excellence

About the role

Lead Device Risk Management, Clinical Evaluation, and Post-Market Surveillance processes across Sanofi as the global process owner. Ensure SOPs align with applicable regulations and industry standards while driving continuous improvement initiatives. Analyze post-market data to identify trends, multi-site impacts, and implement corrective actions. Ensure Device Risk Management Files accurately reflect current product risks and remain updated throughout the product lifecycle. Provide guidance on harmonized risk management approaches aligned with ISO 14971 across all development and lifecycle management programs. Develop new tools, comprehensive training programs and mentor colleagues on process execution, best practices, and risk management methodologies. Ensure project teams utilize appropriate risk analysis tools (FMEAs, PHA) and facilitate dFMEA moderation sessions. Author and maintain post market surveillance deliverables throughout the product lifecycle. Support Design Controls implementation for new product development and design changes, including Design History File maintenance. Partner with quality, compliance, development, and manufacturing teams to ensure transparency, coordination, and patient safety actions.

Responsibilities

• Lead Device Risk Management, Clinical Evaluation, and Post-Market Surveillance processes across Sanofi as the global process owner
• Ensure SOPs align with applicable regulations and industry standards while driving continuous improvement initiatives
• Analyze post-market data to identify trends, multi-site impacts, and implement corrective actions
• Ensure Device Risk Management Files accurately reflect current product risks and remain updated throughout the product lifecycle
• Provide guidance on harmonized risk management approaches aligned with ISO 14971 across all development and lifecycle management programs
• Develop new tools, comprehensive training programs and mentor colleagues on process execution, best practices, and risk management methodologies
• Ensure project teams utilize appropriate risk analysis tools (FMEAs, PHA) and facilitate dFMEA moderation sessions
• Author and maintain post market surveillance deliverables throughout the product lifecycle
• Support Design Controls implementation for new product development and design changes, including Design History File maintenance
• Partner with quality, compliance, development, and manufacturing teams to ensure transparency, coordination, and patient safety actions

Requirements

• BS degree in Engineering, Business, Life Sciences or related science discipline. MS degree is a plus
• 5+ years of medical device industry experience
• 3+ years of relevant experience in in Risk Management and Post-Market Surveillance for medical devices and/or drug-device combination products
• Ability to collaborate effectively with peers, stakeholders, and partners across the organization to positively impact business results; knowledge in problem solving methodologies; deep knowledge of ISO 14971. Knowledge of ISO 13485, MDR (2017/745) and 21 CFR 820
• Experience in complaint management a plus

Qualifications

• Languages: Mandatory English management for Business (written and oral). French or German are a plus
• Technical Skills: ISO 14971 Risk Management, Post-Market Surveillance (PMS), FMEA / Risk Analysis Tools, Regulatory Compliance (MDR / 21 CFR 820), Design Controls & DHF Management

Skills

• Cross-functional Collaboration
• Strategic Thinking
• Attention to Detail
• Stakeholder Influence
• Mentoring & Knowledge Transfer

Benefits

Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Pay

Commensurate with demonstrated experience.

Schedule

N/A