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