Examine Device History Records to perform release of sub-assemblies and finished goods.
Inspect incoming, in-process, and finished parts, and materials for conformance to quality control standards.
Monitor the production line to ensure that production standards are met (GMP).
Recommend adjustments to the assembly or production process.
Trend in-process manufacturing data.
Implement and maintain a quality system per applicable regulatory requirements.
Initiate and participate in the resolution of non-conforming materials.
Responsible for final product release sign-off.
2+ years of Quality Inspection experience, preferably in the medical device arena.
Mechanical capabilities and working knowledge of measurement instruments
High level of attention to details
Good English (written and verbal) communication skills; Good arithmetic skills
Experience with ERP systems- advantage
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