Quality Control Inspector

Quality Control Inspector at Precision Optics Corporation Inc

Gardner, Massachusetts, United States - Full Time

Start Date:

Immediate

Expiry Date: 08 Jan 26

Posted On: 10 Oct 25

Experience:

0 year(s) or above

Remote Job:
Yes

Telecommute:
Yes

Sponsor Visa:
No

Skills:

• Quality Control
• Mechanical Inspections
• Optical Inspection
• FDA QSR
• ISO 13485
• Data Collection
• Problem Solving
• Communication Skills
• Attention to Detail
• Collaboration
• Document Control
• Continuous Improvement
• Calibration
• Recordkeeping
• Production Support
• Regulatory Compliance

Medical Equipment Manufacturing

The Quality Control Inspector, reporting to the Quality Control Supervisor is responsible for all aspects of incoming, in-process, and final inspections, including measurements, recordkeeping, calibration, documentation, production support on an as needed basis and other urgent matters for the Quality Control Department.

• Perform dimensional and visual first article and in-process/final inspection on raw material, parts, gages, and other equipment, accepting material/product or referring for quality review based on findings.
• Prepare inspection reports; ensure material traceability.
• Initiate Nonconformances (NCR) and Supplier Corrective Action Reports (SCARs); facilitate Material Review Board (MRB) meetings.
• Use a variety of fixed and variable measuring instruments.
• Monitor and coordinate Engineering Change Order (ECO) activity across the organization ensuring compliance with the Quality Management System (QMS); support QMS maintenance for compliance with FDA QSR, ISO 13485, and other regulatory requirements.
• Ensure compliance with electronic document control workflows in QCBD or similar document control tool. Ensure documents are being filed and organized.
• Support audits in the role as a “Runner”, extracting documents, review them to ensure regulatory compliance and correctness, and present to the Lead Auditor for presentation.
• Coordinate QA/QC tasks with cross functional teams across the organization: support production and product development teams; review Device History Records (DHRs) for completeness and accuracy; execute receiving procedures & support shipping activities.
• Support and promote continuous improvement initiatives to meet business objectives.
• Maintains a safe and healthy work environment by following standards and procedures and complying with legal regulations.
• Perform miscellaneous duties and projects as assigned and required.

• Minimum 1 year of experience performing mechanical inspections in a manufacturing environment; optical inspection experience preferred.
• Experience working in medical devices and FDA QSR and ISO 13485 preferred.
• Understanding quality control processes, methods, and standards.
• Proficiency with Microsoft 365 apps suite.

• Strong data collection & analysis, problem solving, presentation and communication skills.
• Strong attention to detail.
• Ability to collaborate effectively with cross-functional teams.

High School Diploma or GED required.

This job operates in manufacturing and engineering laboratory environments including ISO class 7 clean rooms. PPE required when in controlled environment rooms or clean rooms.

This role routinely uses standard office equipment such as computers, phones, photocopiers, and filing cabinets.

While performing duties of this job, the employee is occasionally required to stand, walk, sit, use hands to finger, handle, or feel objects, tools, or controls; reach with hands and arms; talk and hear.

In-person, Mon to Fri in Gardner, MA; occasional travel, with periodic presence in the Windham, ME site.

This position involves access to technology that is subject to U.S. export controls. Any job offer made will be contingent upon the applicant’s capacity to serve in compliance with U.S. export controls.

The Quality Control Inspector is responsible for performing inspections on raw materials, parts, and equipment, ensuring compliance with quality standards. This role includes preparing inspection reports, initiating nonconformances, and supporting production and product development teams.