Stryker
10,000+ employees
Founded 1941
⚕️ Healthcare Insurance
🧬 Biotechnology
Healthcare Insurance • Medical Devices • Biotechnology
Stryker is a global leader in medical technology, providing innovative products and services across the healthcare sector. With a presence in countries across the Americas, Asia Pacific, Europe, and the Middle East & Africa, Stryker offers a wide range of medical technologies, including orthopedic implants, surgical equipment, and advanced hospital devices. The company is committed to improving patient outcomes and healthcare efficiency. Stryker continues to expand its global reach, offering localized solutions to meet diverse healthcare needs worldwide.
Staff Internal Quality Auditor
Job not on LinkedIn
🔥 0 minutes ago
🗣️🇪🇸 Spanish Required
📊 Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
Stryker
10,000+ employees
Founded 1941
⚕️ Healthcare Insurance
🧬 Biotechnology
Healthcare Insurance • Medical Devices • Biotechnology
Stryker is a global leader in medical technology, providing innovative products and services across the healthcare sector. With a presence in countries across the Americas, Asia Pacific, Europe, and the Middle East & Africa, Stryker offers a wide range of medical technologies, including orthopedic implants, surgical equipment, and advanced hospital devices. The company is committed to improving patient outcomes and healthcare efficiency. Stryker continues to expand its global reach, offering localized solutions to meet diverse healthcare needs worldwide.
📋 Description
• Responsible for independently leading internal audits to assess compliance and effectiveness of the Quality Management System (QMS). • Partners with site stakeholders to drive compliance, identify risks, and support continuous improvement. • Lead internal audits from planning through execution, reporting, and follow-up • Develop and tailor audit scope, agenda, and plans based on site inputs • Assess compliance to FDA, ISO 13485, MDR/MDD, and company procedures • Document audit results, including nonconformances and observations • Present audit results and insights to site leadership • Support execution of the Global Internal Audit Program • Monitor audit observations and escalate trends or systemic risks • Interface with Site RAQA and Quality leadership teams
🎯 Requirements
• Bachelor’s degree in engineering, science, business administration or related field. • Certified Lead Auditor (or equivalent quality auditing certification) required • At least 2 years of experience auditing in a regulated industry • Fluent in both English and Spanish required • Working knowledge of FDA and ISO 13485 requirements
🏖️ Benefits
• Work Flexibility: Remote
Apply Now
