.Collaboration drives Nordson's success as a market leader in Industrial Precision Solutions and Advanced Technology. Our employees thrive in an environment where we help each other reach our personal best and enable our company to continuously improve and grow, and our customers to succeed. You will find Nordson employees sharing our success by giving back in the communities around the world where we live and work.ESSENTIAL DUTIES & RESPONSIBILITIES:- Perform inspections of purchased parts, subassemblies and/or finished company products according to defined criteria in product documentation; drawing, specification,procedures, or build packages. By visual inspection or measurements.- Competent in all quality processes and procedures according to the training matrix.- Conduct and document process monitoring audits using documented procedures.- Accurately document the results of the inspections, monitoring and testing.- Maintain all controlled document files and test records in a timely and accurate manner.- Monitor critical equipment and instrumentation to ensure calibration status is current.- Identify and communicate defects or suspect materials and initiate the NC (non-conforming) process.- May assist other Quality team members with customer support issues, work instruction creation/updates, document control, control plans, part acceptance criteria, etc.- Effectively communicates quality issues to other functions when observations are made.- Maintain order and cleanliness of Quality stations and cleanrooms to prevent samples-information mixing.- The Quality Inspector is responsible to perform the correct completion of inspection results in the DHR (Device History Record). One of the responsibilities of this position is verify and ensure Reconciliation of the data between the documents and the physical quantities, during the process and at the end of each Lot, ensuring the accuracy of records and maintaining supporting documentation.- Perform review of Device History Records and other documentation for compliance to established procedures and Good Documentation Practices.- Enters appropriate data and or information into ERP/QMS system.- Other duties or projects as assigned.MINIMUM QUALIFICATIONS:- High School Diploma or equivalent.- 2+ year of previous experience as in process inspector.- One year minimum in Medical Devices Industry.- Must be able to use standard measuring/inspection devices (micrometer, gauge pins, microscope, calipers, etc.).- Knowledge of calibration status. As well as Quality Systems documents such as sampling tables.Required Education:- High School Diploma or equivalent.Knowledge, Skills & Abilities (KSA's):SKILLS AND ABILITIES:- Ability to read and comprehend instructions, short correspondence, and memos in both English and Spanish.- Ability to interpret drawings with medium degree of complexity.- Ability to solve practical problems.- High level of attention to detail