Are you passionate about being part of a Team that will become the most trusted medical device machining service provider? Are you tired of mundane cubicle roles? Join Team Orchard Park as a Quality Technician, state-of-the-art, inspection equipment and realize your full potential as a High Impact member of our Quality team. New employees are eligible for the following benefits effective date of hire!Medical, dental, and vision benefitsCompany-paid life insuranceGenerous Paid time off and 10 paid Holidays401k Plan with Company MatchTuition Reimbursement Attendance Bonus paid monthly GROWTH: This is an outstanding opportunity for a Technician that has an attention to detail, thrives in cross-functional teams, and is ready for the next big challenge. You will be working in a highly dynamic work environment that encourages and promotes developmental growth in many areas. MISSION: We collaborate and innovate with our customers to provide the highest quality, life enhancing medical devices in the world. Key Responsibilities: Calibration Support Assist with maintenance of systems that monitor the accuracy of all measurement and test equipmentAssist with calibration as required for all company owned equipment as well as personal tools.Assist with the repair of gages as needed; if unable to do internally, send to an outside repair service and /or request a replacement Manufacturing Support Troubleshoot Smartscopes/CMM and Vici equipmentInspect vendor work with the Smartscope V.M.M.Internal AuditorIn-process inspection as requiredInspect vendor supplied components / assemblies. Assist suppliers in duplicating our inspection techniques and meeting our product specificationsLaser inspection (First piece Laser certification)Use all gaging methods in the facility, including roundness checker, profilometer, and height standsDevelop expertise in GD&T and other blueprint and dimensioning methodsTrain associates on laser inspection and assist in obtaining certification Final Product Release Assist with documentation of any discrepancies as appropriate Control of Non-Conforming material/ parts are Quarantined to prevent shipmentCertify documentation (i.e.: Certification, first article data, process capability study, etc.) prior to shipmentVerify packaging matches specified requirements (where indicated) or is adequate if no specific requirements existVerify customer purchase order requirementsVerify /sign completed shipment verification review form Qualifications Technical degree and 3 years’ equivalent experience in similar regulated field Medical Device experience strongly preferredLaser inspection experience preferredExperience with MS-Word, Excel, Access, and Power Point for word processing and documentation supportGood teamwork and communication skills to facilitate training and group problem solvingMust be able to complete multiple prioritized tasks with minimal direct supervision, while maintaining focus on preventative activitiesComplete all job-specific required trainingAbility to understand/comply with the FDA’s Quality Systems Regulations (QSR) and ISO 13485:2003 standardsASQ certification as a CMI, CCT, or CQT is required within one year of being in the position CLICK HERE FOR A SITE TOUR! ** All job offers are contingent on passing a background check and drug test (including THC) #INDLP.