Job Title: Devie - Senior Quality Engineer, Invitro Diagnostics
Location: Cambridge, MA
About the Job
The Senior Quality Engineer – IVD Devices is a senior subject matter expert responsible for ensuring the quality, safety, and regulatory compliance of IVD devices across the full product lifecycle—from early development through commercialization and lifecycle management. Partnering with the Senior IVD Director, this role requires deep technical and regulatory expertise including EU IVDR, FDA 21 CFR Part 809/812/820, ISO 13485, ISO 18113, and ISO 15189. The incumbent serves as a strategic quality partner to cross-functional teams including R&D, Regulatory Affairs, Manufacturing, Clinical, and Laboratory Operations, providing expert guidance on design controls, analytical validation, clinical performance evaluation, and post-market quality requirements.
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
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
IVD Quality Management System: Contribute to the design and implementation of a fit-for-purpose IVD QMS aligned with ISO 13485, EU IVDR, and MDSAP. This includes working with key stakeholders to establish phase-appropriate processes spanning research, development, validation, and commercial lifecycle. Harmonize QMS practices across global functions and develops lean, scalable processes suitable for a growing organization in the IVD space.
IVD Regulatory Compliance: system leadership across IVD design, evidence generation, labeling, and lifecycle management. Serve as primary Quality interface with FDA and EU Notified Bodies for IVD, ensuring inspection readiness within the device domain. Support regulatory submissions in the U.S. as well as EU IVDR including conformity assessments. Contribute to performance evaluation reports and technical files while ensuring strong linkage between analytical validation and labeling requirements. Ensure labeling and Instructions for Use (IFU) compliance with ISO 18113 and 21 CFR 809.10. Drive global regulatory harmonization, anticipate Notified Body expectations, and integrate compliance requirements into design processes from early development.
End-to-End IVD Lifecycle Quality: Provide quality leadership across assay design, development, verification, validation, and commercial manufacturing. Ensure traceability from user needs through design inputs, outputs, validation, and clinical evidence. Drive consistent application of design controls and DHF/Technical File management. Oversee analytical performance studies (sensitivity, specificity, precision, linearity, interference, reference intervals). Contribute to technical documentation/design dossier, performance evaluation (scientific validity, analytical performance, clinical performance), support clinical evidence /studies (when required), Post-Markey Surveillance, risk management (ISO14971), Interactions with laboratories (ISO 15189)
Laboratory & Clinical Study Quality: Establish quality frameworks for internal development laboratories and external partner labs/CROs ensuring compliance with CLIA, CAP, and ISO 15189. Lead quality oversight for IVD clinical performance studies including protocol review, site qualification, monitoring, and data quality. Ensure alignment with ISO 20916 and regulatory requirements.
Supplier & Material Quality: Conduct new vendor audits, qualification and monitoring, and overseeing the quality aspects of IVD development, validation and patient testing performed by third parties
Post-Market Quality & Continuous Improvement: Establish and manage nonconformance, deviation, CAPA, complaint handling, and vigilance reporting systems. Define and implement post-market performance follow-up (PMPF) strategies. Drive continuous improvement through data-driven quality metrics.
Cross-Functional Collaboration: Work closely with IVD development teams, Regulatory Affairs, Clinical, and Laboratory Operations. Balance scientific understanding with quality rigor and business objectives to support IVD commercialization and lifecycle management
About You
Basic Qualification
Bachelor's degree in Engineering, Biomedical Engineering, Biochemistry, Molecular Biology, Analytical Chemistry, or related scientific discipline, with 10+ years in quality management within IVD or closely related diagnostic fields.
Advanced degree (MS/PhD) preferred
Minimum 1 year in regulatory affairs or quality management systems for IVD medical devices is preferred
Strong leadership experience required
Hands-on experience with assay development and validation
Laboratory quality systems implementation and management
Clinical and performance study support
Direct experience with Analyte Specific Reagents and Companion Diagnostics
Proven track record building or transforming QMS in developing organization
Experience supporting IVDs from concept through commercialization
Additional Preferred Experience:
Manufacturing operations experience
Drug-device combination products knowledge
Technical Skills:
Quality Management Systems & Regulatory Compliance:
In-depth knowledge of ISO 13485:2016, EU IVDR (2017/746), FDA 21 CFR Part 820 (QSR), and 21 CFR Part 809 (IVD regulations)
Proven track record implementing and certifying QMS systems across multiple sites
Working knowledge of MDSAP (Medical Device Single Audit Program) requirements
Comprehensive GxP knowledge and experience in implementation and maintenance of compliant systems
IVD-Specific Standards & Requirements:
Strong expertise in ISO 18113 series, ISO 15189, and CLSI guideline
Knowledge of IEC 62304 (software lifecycle) and IEC 62366-1 (usability engineering) for IVD products with software/SaMD components
Understanding of ISO 14971 risk management principles applied to IVD devices
Experience with technical documentation, performance evaluation, and post-market obligations under EU IVDR
IVD Development & Validation:
Demonstrated experience with design controls and DHF/Technical File management for IVD devices
Hands-on experience with analytical performance studies (precision, accuracy, linearity, interference, reference interval studies)
Experience with process validation (IQ/OQ/PQ), analytical method validation, and design transfer for IVD manufacturing
Knowledge of assay development lifecycle and validation requirements
Risk Management & Problem Solving:
Proficiency in risk management tools and methodologies (FMEA, FTA, risk-benefit analysis)
Strong problem-solving methodologies and root cause analysis capabilitie
Experience with complaint handling, MDR/vigilance reporting, and post-market surveillance systems
Emerging Technologies:
Familiarity with SaMD quality considerations including algorithm validation, cybersecurity, and AI/ML-based IVD products
Ability to navigate complex global regulatory environments and drive organizational alignment
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 and Affirmative Action employers committed to a culturally diverse 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.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
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US and Puerto Rico Residents Only
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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:
$133,500.00 - $192,833.33All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.