2nd Shift Quality Inspector

2nd Shift Quality InspectorMicron Solutions is a multifaceted contract manufacturing organization specializing in thermoplastic injection molding, precision machining and finishing, and silver-plated medical sensors for disposable electrodes. We partner with companies of all sizes to deliver manufacturing and assembly solutions that support their success. Our 120,000-square-foot facility in Fitchburg, MA supports projects from concept through commercialization.The 2nd Shift Quality Inspector is responsible for performing inspection activities, documenting results, and communicating findings to Quality and Operations leadership. This role plays a key part in identifying nonconforming products, supporting investigations into process issues, and contributing to corrective and preventive actions.This position requires accurate data entry, recordkeeping, and adherence to quality standards in a regulated manufacturing environment. Applicants must be legally authorized to work in the United States. Micron Solutions is unable to provide employment visa sponsorship now or in the future for this position and is unable to offer relocation assistance.Schedule: Monday–Friday, 3:00 PM – 11:00 PMInspection & TestingPerform product inspection using a variety of precision measurement tools and equipmentProperly set up parts, run established measurement programs, and interpret results (pass/fail)Inspection equipment includes, but is not limited to: Coordinate Measuring Machine (CMM), vision systems (Keyence, Micro-Vu), optical comparators (standard and eCAD), micrometers, calipers, and drop indicators, pull-force and hardness testersQuality Documentation & Data ManagementAccurately complete and maintain quality records, logs, and reportsPerform data entry to support trending and performance monitoringConduct documentation review and dimensional verification of incoming materialsNonconformance & MRB SupportIdentify, segregate, and tag nonconforming materialsLog and document nonconforming product detailsParticipate in Material Review Board (MRB) activities, including evaluation and disposition supportProvide input on product condition and potential impactContinuous Improvement & ComplianceIdentify opportunities for corrective and preventive actions (CAPA)Support follow-up and effectiveness checks under guidance of Quality EngineeringPerform in-process, final, and release inspectionsComplete First Article Inspections (FAI) following established proceduresSupport validation activities with measurement and documentationPerform in-house gage calibrations per work instructionsQualificationsEducation & ExperienceHigh School Diploma or GED requiredSkills & KnowledgeAbility to read and interpret technical drawings, specifications, and work instructionsBasic computer skills, including proficiency with Microsoft OfficeExperience with standard dimensional inspection tools (calipers, micrometers, comparators, etc.)Ability to operate advanced inspection equipment (e.g., CMM, vision systems)Working knowledge of ISO 13485 standards, FDA 21 CFR Part 820, Statistical Process Control (SPC) principlesAdditional RequirementsStrong attention to detail and organizational skillsEffective communication and ability to follow verbal and written instructionsAbility to work independently in a fast-paced manufacturing environmentMust be able to work the assigned shift: Monday–Friday, 3:00 PM – 11:00 PM