2nd Shift Quality Inspector

2nd Shift Quality Inspector

Micron 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 PM

Inspection & Testing

• Perform product inspection using a variety of precision measurement tools and equipment
• Properly 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 testers

Quality Documentation & Data Management

• Accurately complete and maintain quality records, logs, and reports
• Perform data entry to support trending and performance monitoring
• Conduct documentation review and dimensional verification of incoming materials

Nonconformance & MRB Support

• Identify, segregate, and tag nonconforming materials
• Log and document nonconforming product details
• Participate in Material Review Board (MRB) activities, including evaluation and disposition support
• Provide input on product condition and potential impact

Continuous Improvement & Compliance

• Identify opportunities for corrective and preventive actions (CAPA)
• Support follow-up and effectiveness checks under guidance of Quality Engineering
• Perform in-process, final, and release inspections
• Complete First Article Inspections (FAI) following established procedures
• Support validation activities with measurement and documentation
• Perform in-house gage calibrations per work instructions

Qualifications

Education & Experience

• High School Diploma or GED required

Skills & Knowledge

• Ability to read and interpret technical drawings, specifications, and work instructions
• Basic computer skills, including proficiency with Microsoft Office
• Experience 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) principles

Additional Requirements

• Strong attention to detail and organizational skills
• Effective communication and ability to follow verbal and written instructions
• Ability to work independently in a fast-paced manufacturing environment
• Must be able to work the assigned shift: Monday–Friday, 3:00 PM – 11:00 PM