Metrology Specialist II

Responsibilities The Metrology Specialist II is responsible for performing manufacturing inspections. The Metrology Specialist II works under the guidance of the In-Process Quality (IPQ) Team Lead and IPQ Supervisor and is responsible for ensuring compliance with Quality Management Systems policies and procedures, regulatory standards, and inspection of GBO NA products. The role will be assigned to a 2-2-3 Twelve Hour Shift Schedule. The successful completion of onboarding, training, and inspection qualification in injection molding for pre-analytic components. Perform dimensional part inspections using a CMM and various metrology instrumentation Perform inspections and IPQ releases for semi-finished and finished goods according to valid procedures, including injection molding and final assembly departments. Conduct activities to meet departmental Safety, People, Quality, Responsiveness, and Cost KPIs. Provide timely measurement and reporting for Quality Assurance and Engineering validation activities including IQ, OQ, PQ, Product Verifications, Engineering Studies, and Measurement Requests. Contribute to mentoring and training IPQ team members. Support maintenance of testing equipment, including procurement, troubleshooting, scheduling, and performance of internal/external calibrations as required. Assist in the design and development of new measuring techniques, equipment, and fixtures. Perform CMM programming and measurement validations in collaboration with Quality Engineering. Review and close inspection records to ensure timely compliance. Accurately document and submit IPQ inspection records following Good Manufacturing Practice (GMP). Carry out periodic cycle counting and order IPQ laboratory supplies as needed. Perform other administrative duties to ensure IPQ operational readiness as required. Administer and approve metrology proficiency evaluations for the IPQ team. Evaluate products, control non-conforming products, and release IPQ according to valid procedures. Handle ERP transactions such as stock transfers and quality holds (SAP). Report and troubleshoot inspection devices/equipment and Laboratory Information Management System (Babtec). Qualifications Minimum associate's degree in technology, science, or math fields; equivalent experience considered. Minimum 3 years of experience in an ISO, GMP, NIST, or similar regulated manufacturing environment; relevant technical experience preferred. Minimum 3 years experience in GD&T, CMM programming, and operation of tactile and optical CMM systems (Zeiss Calypso and Mitutoyo MCOSMOS). Intermediate-level experience with laboratory testing equipment, instrumentation, and analysis, as well as laboratory data processing and review. Intermediate-level MS Office skills. Physical Requirements Must be able to stand and walk for up to 8–12 hours. Must be able to lift up to 50 lbs. Must have appropriate vision to perform detailed quality inspections as outlined in SOPs or TPs. Equal Opportunity Statement We provide equal opportunities for everyone and see diversity as our strength. Therefore, we welcome all applicants – regardless of characteristics such as gender, age, background, social status, sexual orientation, religion, or mental and physical abilities. We have set the goal of empowering women and increasing female leader representation. We foster an inclusive work environment and encourage all individuals to apply. #J-18808-Ljbffr Greiner Bio-One Americas