Quality Inspector I

Quality Inspector IJoining 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 Quality Inspector I will be responsible for performing quality assurance inspections on purchased components, manufactured sub-assemblies and final product. The Quality Inspector will perform all duties in accordance to the requirements of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to be familiar with and able to measure critical dimensions.Position is a 4 day/10hour shift (M-TH)Essential Duties And ResponsibilitiesPerform inspection by using a variety of inspection measuring and test equipment to determine acceptance or rejection of material or parts.Perform first article, incoming/receiving, and in-process inspections of materials or parts; determine acceptance or rejection after inspection and/or testing of materials, parts, and/or equipment.Interpret and work within the guideline of drawings, specifications, charts, procedures, and other data to determine acceptance or rejection of materials.Read and interpret sampling plan as per the American national standard institute (ANSI).Assist in training new associates according to the Quality System Regulations and company SOPs as applicable.Maintain accurate and current inspection and/or testing records such as and not limited to Material Certifications, Inspection/Test Results and reports, Certificates of Conformance, Rejection reports/tags, as required by applicable procedure and/or specification.Assist with reviewing inspection reports, completed Quality forms, logbooks, and associated Quality forms.Inspection requirements include training and working in classified clean rooms as necessary to perform in process inspections.Perform line clearances and quality reviews in manufacturing, labeling, or other assigned areas during manufacturing activities.Maintain records of inspection and all testing performed on the appropriate test records.Assist in physical moving and labeling of non-conforming material and customer returned material, including rework, scrap, and return to vendor.Maintain the QC inspection areas in an orderly fashion conducive to carrying out safe and efficient inspections and procedures.May also perform other related duties, responsibilities, and special projects as assigned.While undertaking the essential duties and responsibilities of the position, the employee must repeatedly sit, listen, speak, and write in English. The employee is required to go to all areas of the company. Employee is required to enter cleanrooms while adhering to Standard Operating procedures. The employee may be required to periodically lift and/or move up to 50lbs.Important: Role requires employees to pass a visual acuity test. Vision aids, such as glasses or contact lenses, are allowed and must be worn during visual inspections if needed to pass the test.Salary Pay Range: $19.19 - $25.43 USD HourlyIntegra 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.