Global Medical Device Compliance Lead
Listed on 2026-10-07
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Engineering
Regulatory Compliance Specialist, Biomedical Engineer -
Quality Assurance - QA/QC
Regulatory Compliance Specialist
Stryker Group in Irvine, CA is seeking a Staff Quality Compliance Engineer to lead global regulatory compliance across the product lifecycle. You will provide technical leadership for standards management, assess regulatory changes, and implement actions to keep products and quality systems aligned with evolving requirements.
You will collaborate with cross-functional teams, support audits as a subject matter expert, review test protocols and reports for regulatory conformity, and guide teams
We are seeking a motivated Global Medical Device Compliance Lead to join Stryker Group in Irvine, CA, United States.
Join Stryker Group and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Global Medical Device Compliance Lead role at Stryker Group, based in Irvine, CA, United States.
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