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Integra LifeSciences is seeking a Quality Inspector on site in the United States. Responsibilities include inspecting raw materials, in-process assemblies, and finished goods to ensure compliance with ISO 13485, FDA 21 CFR 820, and GMP standards.
The role emphasizes accurate documentation, lot-history review, and participation in corrective actions. The ideal candidate has 1–5 years of experience in regulated manufacturing, strong attention to detail, and proficiency with MS Office and eQMS
Integra LifeSciences is seeking a Quality Inspector on site in the United States. Responsibilities include inspecting raw materials, in-process assemblies, and finished goods to ensure compliance with ISO 13485, FDA 21 CFR 820, and GMP standards.
The role emphasizes accurate documentation, lot-history review, and participation in corrective actions. The ideal candidate has 1–5 years of experience in regulated manufacturing, strong attention to detail, and proficiency with MS Office and eQMS