QC Inspector II

Changing lives. Building Careers.

Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.

The QC Inspector II works in Quality Control to perform various inspections throughout the manufacturing process including incoming receiving, in-process, final inspection, labeling, packaging, and final release. Verifies that the engineering drawing, work order, documents, etc. matches the part number inspected. Completes documentation to either release materials or initiate non­conformance reports. The QC inspector II examines products and materials for defects or deviations from specifications. May perform receiving of products and take inventory of raw materials. Reviews calibration of equipment performs internal calibration as necessary.

• Reads engineering drawings, and specifications and interprets necessary information including dimensions, tolerances, etc.
• Monitors components, labels, products to ensure that they meet production standards.
• Inspects, tests, or measures materials or products being produced.
• Measures products using a variety of equipment including rulers, calipers, gauges, micrometers to characterize components and products.
• Accepts or rejects finished items.
• Maintains both hardcopy and electronic files of inspected materials.
• Inputs data into a quality database.
• Initiates non-conformance reports for material that does not meet specification. Places non-conforming material to correct area after disposition.
• Quarantines non-conforming product.
• Places acceptable product into raw material or finished goods stock.
• Determines sample lot size from AQL table.
• Suggests improvement to documentation, inspections, drawings, etc. for clarity, efficiency, process improvements, etc.
• Perform internal calibration of equipment as necessary.
• Perform receiving of materials from suppliers.
• Perform inventory counts of raw materials.
• Documents and prints labels for raw material and finished goods.
• Review final product labels for placement onto finished goods.
• Other duties as assigned by the supervisor.
  
  

Qualifications:

The requirements listed below are representative of the knowledge, skill and/or ability required for his position.

• Associate’s degree or equivalent work experience
• Two (2) or more years of laboratory experience
• Experience in QC inspection, cleanroom manufacturing, and medical device start-up
  
  

Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.

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