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Medical Device Inspector
1 week ago
As a Quality Assurance Specialist at Integra LifeSciences, you will be responsible for upholding quality standards, maintaining compliance, and supporting operational efficiency in our GMP-rated, FDA, and MOD-regulated environment. This is a critical role that requires a high degree of attention to detail and a commitment to delivering high-quality results.
Your responsibilities will include:
- Performing inspections and tests of finished devices, sub-assemblies, and components.
- Reviewing and interpreting engineering drawings, material specifications, and test documents.
- Supporting incoming inspection processes using various metrology equipment.
- Collaborating with supply chain and manufacturing teams to plan inspection activities.
- Managing non-conforming materials and communicating issues to management.
We are looking for an individual with a minimum of 2 years of experience in an FDA and ISO 13485 regulated manufacturing facility, preferably in a quality inspection role. Strong communication skills and the ability to work effectively in a team environment are essential for this position.