Description: Is responsible for carrying out the precise inspection of all incoming components, raw material delivered to our Company, while following the appropriate inspections and accompanied with the appropriate documents. Fills out the appropriate control documents with respect to inspection materials and maintains all incoming inspection duties. Performs tests to facilities equipment, using different testing instruments and machines. May prepare reports of test results and other related data, using computer or other instruments as required. ESENTIAL DUTIES AND RESPONSIBILITIES: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. 1. Is responsible for receiving, verifying, handling all incoming raw materials and document results as per applicable procedure. 2. Inspect all incoming raw material, components and other production related materials, following the appropriate QCIC's blue prints or specifications, S.O.P.'s TM, and determines the disposition of such goods. 3. Inspection reports and documentation must be kept on file for future actions, reference, etc. 4. Verifies that stated material quantities are actually received from the receiving department. Checks the accompanying documents to ensure the completeness of the same, and the use of the most recent revision change. 5. Fill out any control documentation on their activities, as required by the area supervisor. 6. Maintains all Discrepant Material Reports until the final disposition of the product is made. 7. Assures that the quantities are correct prior to being released and assures that the final disposition on the Discrepant Material has been documented. 8. Assures all material dispositioned "Return to Supplier" is properly handled to the appropriate department. 9. Distributes copies of the Discrepant Material Report according to the established procedure. 10. Assures no lots are being released prior to completing all inspections and has all the appropriate documents. 11. Assures that quantities are correct prior to completing all inspections and has all the appropriate documents. 12. Assures that work performance is according to priorities established and set priorities on this area based on Production Control Schedule. 13. Sets schedules for the accomplishment of goals and objectives set forth by his supervisor. 14. Will maintain current systems such as Vendor Rating, Vendor Qualification, Quarantine Cage and others. 15. Bring to the attention of the area supervisor any unusual condition or defects in receiving materials. Holds received material in the Incoming Inspection Quarantine Area maintains control over it until disposition of the same has been reached. 16. Maintains all equipment used for testing and measuring, and keeps the working area in a clean, well-organized condition. 17. Fill out any control documentation on their activities, as required by operating procedures or requested by the area supervisor. 18. Provides the supervisor with daily, weekly and monthly reports on the inspection operation. 19. Is responsible for keeping documents, prints and QCIC's in good conditions as well as organized. Is responsible for the issuing of material required under quarantine. 20. Is responsible for releasing the material after all inspections have been completed. Will handle bulky materials and will carry heavy boxes. 21. Analyzes sterilization and toxicity results and all other test results of raw materials and prepares required records and documentation. 22. Is not limited in helping in the implementation of any other specified project assigned. 23. Identifies and recommends the acquisition of the necessary instruments, equipment and supplies required to give complete instrumentation services to operations. 24. Updates procedure of the area of responsibilities as required. 25. Responsible for submitting and follow-up of corrective actions concerning discrepancies found within areas of responsibilities. 26. MRB Assistance 27. Maintain well organized and updated all concerning procedures related to the department. 28. Troubleshooting of equipment use in the area. 29. Perform other projects assigned by the Q.A. Manager / Supervisor (Validations, Reports, etc.). 30. Prepare SPC control graphs according to data submitted by QA process. DESIRED MINIMUM QUALIFICATIONS • High School graduate or equivalent. • Previous experiencie in QC/QA. • 1 to 2 years’ experience in a medical device manufacturing environment preferred. • Knowledge of basic math concepts, graphs interpretation, and use of procedures, and inspection methods. • Knowledge of statistical process control techniques. • Ability to read, understand drawings and written documents in English. • Ability to work using testing instruments and manual equipment. • Knowledge of GMP, ISO Standards (9002), NIST Standard **Pay Details:** $10.50 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: + The California Fair Chance Act + Los Angeles City Fair Chance Ordinance + Los Angeles County Fair Chance Ordinance for Employers + San Francisco Fair Chance Ordinance