Job Information
Stryker Ingénieur Qualification/Validation in Pusignan, France
At Stryker, we’re not just building medical devices—we’re improving lives. As a Fortune 100 company recognized among the top workplaces in Europe, we are united by one mission:
“Together with our customers, we are driven to make healthcare better.”
As part of our Global Quality Operations - QA Validation team, you’ll play a critical role in ensuring our systems and processes meet the highest standards of safety, performance, and compliance. If you thrive in collaborative, cross-functional environments and bring both precision and curiosity to your work—this is your opportunity to make a real difference.
Your mission:
Lead Validation Projects : Plan, execute, and document Equipment Qualification (EQ), Computer System Validation (CSV), and qualification of Buildings, Facilities, Utilities (BFU) in alignment with global and local standards.
Collaborate Cross-Functionally : Work closely with global and local teams across multiple functions to support validation strategy, execution, and process optimization.
Document Meticulously: Author validation deliverables (FAT, SAT, IQ, OQ, EQ, MSA) within our eVLMS (ValGenesis), maintaining a clear and compliant validation lifecycle.
Apply Engineering Best Practices : Use quality engineering tools, process development methods, and statistical analysis to ensure every process delivers consistent, reliable results.
Evaluate and Analyze : Run process and equipment tests, analyze data, and ensure validation outcomes meet regulatory and internal requirements.
Contribute to Continuous Improvement : Support remediation projects and ongoing process development by proactively identifying areas for improvement.
Champion Quality and Compliance : Help ensure Stryker maintains its reputation for world-class quality by upholding FDA, ISO, and GMP standards.
Build Knowledge and Share It : Stay informed on regulatory and technological developments and contribute to a culture of learning, safety, and innovation.
Your profile:
Bachelor's degree in Engineering , Medical Science , Quality , or related fields
Familiarity with FDA, ISO, and GMP standards
Strong understanding of validation methodologies and statistical tools such as sampling plans, Gage R&R, and process capability
Experience with validation documentation and lifecycle systems (e.g., ValGenesis)
Strong interpersonal and communication skills—able to collaborate across cultures and disciplines
Proficiency in French (written and spoken) and professional English
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.