Lead Auditor CRS

Conduct UL GMP certification audits for manufacturing suppliers across Southeast Asia (SEA), ensuring compliance with program standards. Achieve KPI and productivity targets while assessing suppliers in the Medical Devices, Food, Supplements, and Pharmaceuticals industries.Job Responsibilities:• Conduct audits independently and collaboratively, ensuring compliance with cGMP and quality management standards (FDA CFR 820, CFR 210/211, ISO...

• Bachelor's degree in Electrical & Electronic Engineering with 4+ years of experience in manufacturing or quality assurance within the Medical Devices, Cosmetics or Pharmaceutical industries.• 2 - 3 years’ GMP audit experience in the same industries.• Strong knowledge of FDA CFR 820, CFR 210/211, ISO22716 regulations is a must.• Willing to travel across...