Metrology Specialist II

Your challenge

Responsibility:
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.
•    Performing dimensional part inspections using a CMM and various metrology instrumentation
•    Performing inspections and IPQ release for semi-finished and finished goods according to valid procedure(s). This includes injection molding and final assembly departments.
•    Performing activities to meet departmental Safety, People, Quality, Responsiveness, and Cost KPI’s.
•    Performing timely measurement and reporting for Quality Assurance and Engineering validation activities including IQ, OQ, PQ, Product Verifications, Engineering Studies, Measurement Requests, etc.
•    Contributing to mentoring and training IPQ team members.
•    Supporting maintenance of testing equipment including procurement, troubleshooting, scheduling, and/or the performance of internal/external calibrations as required.
•    Assist in the design and development of new measuring techniques/equipment/fixtures.
•    Performing CMM programming and measurement validations in collaboration with Quality Engineering.
•    Performing timely compliance review and closure of inspection records.
•    Accurately documenting and submitting IPQ inspection records following Good Manufacturing Practice (GMP). 
•    Performing periodic cycle counting and ordering of IPQ laboratory supplies as needed. 
•    Performing other administrative duties to ensure IPQ operational readiness as required.
•    Administer and approve metrology proficiency evaluations for the IPQ team.
•    The evaluation of products, control of non-conforming products, and IPQ release according to valid procedures.
•    Responsible for ERP transactions such as stock transfers and quality hold (SAP).
•    Responsible for reporting and troubleshooting inspection devices/equipment and Laboratory Information Management System (Babtec).

Your Profile

Job Requirements:
The following criteria are considered minimums for the role:
•    Minimum associates 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 the 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 SOP’s or TP’s