Job Summary

The Quality Control Inspector is responsible for the inspection of the product at different levels of the process, in order to assure that the material meets or exceeds the requirements set forth in Company documents and procedures. The responsibilities include material handling in support of production.                                                                                                                        

Duties & Responsibilities

Perform Receiving, In-Process, and Final inspections of product per AP (acceptance procedure) documents Generate and complete Quality Reports in accordance with released acceptance procedures, drawings, bill of materials, assembly master records, and device master records requirements Perform functional testing per AP (acceptance procedures) and DR (drawing) requirements Release / approval of product labels  Review of work / job orders for compliance to internal documentation such as AMR (assembly master records), DMR (device master records), DR (drawings), DHR (Device History Record), and MB (bill of materials) Identification, segregation, and NCR generation for nonconforming products and materials Keep up to date with document revision changes as they affect inspections Movement of material to designated locations in support of inspections, MRB, RMA, and Inventory processes.  The material handling will include but not be limited to the physical movement of material in the warehouse and/or QC Areas, use of pallet jacks, packing and unpacking of material, palletizing material, lifting material, and verification of material quantities and documents Perform other duties or special projects as assigned

Minimum Qualifications

Three years of experience as a Quality Control Inspector (or similar role) within the medical device industry; or equivalent combination of education and related experience in any industry PC literate with good skills in MS Office (Word and Excel) programs Working knowledge of GDP (Good Documentation Practices) Good verbal and written communication skills Must be able to work with minimum supervision

Preferred Qualifications

Prior experience with quality control systems Familiar with Part 820 Quality Systems Regulation Familiar with ISO 13485 Standards Familiar with GMP (Good Manufacturing Practices) Familiar with Agile, and Expandable ERP systems

Education

High School diploma or GED is required.  College degree is preferred.

Compensation

The anticipated Hourly Rate range for this position is $20-26 Per Hour plus benefits.  Actual placement within the range is dependent on multiple factors, including but not limited to skills, education, and experience. 

Masimo offers benefits such as Medical, Dental, Vision, Life/AD&D, Disability Insurance, 401(k), Vacation, Sick, Holiday, Paid Maternity Leave, Flexible Spending Accounts, Voluntary Accident, Critical Illness, Hospital, Long-Term Care, Employee Assistance Program, Pet Insurance, on-site Wellness Clinic, Fitness Center and Cafe. All benefits are subject to eligibility requirements.

Physical requirements/Work Environment 

This position primarily works in an office, laboratory, and manufacturing environment. It requires frequent sitting, standing and walking. Daily use of a computer and other computing and digital/mechanical devices is required. Must be able to regularly lift up to 35 pounds. May sit or stand for extended periods. Some local travel is necessary, so the ability to operate a motor vehicle and maintain a valid Driver’s license is required. 

The physical demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.