Responsibilities:

• Inspect incoming medical device components, raw materials, and sub-assemblies using precision tools (calipers, micrometers, height gauges).
• Perform final product inspections to verify compliance with specifications and regulations.
• Accurately document inspection results per Good Documentation Practices (GDP).
• Identify/report non-conformances and support root cause investigations.
• Maintain inspection records and assist in audits.
• Work with Quality Engineering and Manufacturing to resolve quality issues.

Requirements:

• Preferred: Experience in regulated medical device manufacturing.
• 2+ years of experience in incoming and final product inspections.
• Knowledge of cGMP, ISO 13485, and quality standards.
• Ability to interpret engineering drawings, work instructions, and specs.
• Proficient with inspection tools (optical comparators, microscopes, calipers).
• Detail-oriented, independent, and able to work in a fast-paced setting.