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The Quality System at Maine Manufacturing encompasses all production infrastructure including:

• Clean Room Spaces (Class 100,000 clean room)
• Incoming and in-process Quality Control laboratories
• Final audit Quality Control laboratories
• All equipment, facility-wide

The Quality Department at Maine Manufacturing provides uninterrupted support for evaluation and performance testing of your product.  Process documentation, specifications and records are all managed as part of the quality system and serve as an excellent foundation to propel continuous improvements at Maine Manufacturing.

As an ISO 9001:2008 certified manufacturer, Maine Manufacturing follows traditional Quality Managements systems.  The system is anchored by our Quality Manual which describes what policies are in place to comply with the requirements of the International Standard.  Moreover, the Quality Manual describes the overall Quality Management System, Management Responsibility, Resource Management, Product Realization, along with Measurement, Analysis and Improvement.

Within the Quality Management System, Maine Manufacturing follows traditional Layers of control and oversight including following instructions, BOM’s, Routings, and Work Instructions’ responsibility of individuals performing specific tasks. Additionally, oversight includes the use of calibrated tools, maintained equipment and test stations.  Finally, we conduct Internal Audits by the Audit Coordinator or their Representatives to ensure proper adherence to our Quality Management System.


Maine Manufacturing has implemented a highly automated, robust, scalable web based software system as an integral component of its QMS.  The system to help control documents and improve communication and encompasses:


• Document Control

-       Policies & Procedures
-       Specifications
-       Drawings
-       Documents of External Origin

• Engineering Change Requests (ECR)

• Non-Conforming Material Requests (NCMR)

• Customer Complaints

• Internal Audits

• Corrective & Preventive Actions (CAPA)

• Management Review

• Preventive Maintenance

• Training Records

• Records of External Origin

Above all else, we strive to delight our customers by demonstrating our commitment to comply with requirements and to continually improve the effectiveness of our Quality Management System, and ultimately working together to hit our delivery and quality targets.