**About Us**:
MASS Precision Inc. is a global manufacturer with over 30 years of experience excelling in the custom contract manufacturer of electronic chassis, frames, fabrications, and turn-key electromechanical assemblies built to customer specifications.
MASS manufactures medical devices and military electronics for some of the largest companies in Silicon Valley.
We are constantly improving our operations and looking for new ways to meet our Customer's needs through continuous improvement.
**General Job Description**:
**Duties & Responsibilities**:
- Responsible for developing, assisting, and improving the organizations Quality Management System to ensure all processes, components, subassemblies, and finished products are developed and manufactured with applicable ISO requirements.
- Responsible for the management and productivity of the Quality Inspecting, Quality Engineering, and Document Control teams.
- Ensure the development and validation of appropriate test methods for product and process performance.
- Support product complaint system and investigations to ensure that complaints are documented, investigated and closed in a timely manner.
- Manage the non-conforming materials review in collaboration with operations to ensure timely reporting, analysis, and resolution of non-conforming material/product defects.
- Address systematic quality issues with suppliers or internal groups.
- Create, review, and approve Quality System Documents.
- Record and report trending analysis (Quality Metrics) on a monthly basis.
- Oversee management of Calibration System for fixtures, tools and equipment.
**Education, Training & Experience**:
- Bachelor's Degree in Engineering, or Equivalent
- 5-10 Years Experience in a Manufacturing Environment with a focus in Sheet Metal, Machining, Paint, Weld, and Electro-Mechanical Assembly
- NASI Certification Preferred
- Automotive or Medical Quality Experience Preferred
**Knowledge, Skills & Abilities**:
- Must understand, follow and comply with regulatory requirements as applicable to various processes.
An understanding of ISO standards (9001 &13485) required.
- Strong working knowledge of design controls, risk management, and manufacturing process controls required.
- Strong technical writing skills and ability to create technical protocols/reports as well as manufacturing/inspection procedures required.
- Able to write or correct QMS documents
- Excellent organization, planning, and problem-solving skills
- Good interpersonal and communication skills; team mentality with the ability to motivate
- Ability to review, analyze, summarize, and interpret data, draw conclusions and make appropriate recommendations
- Ability to create and provide training
- Good statistical and numerical ability
- Proficient with MS Office including Word, Excel, and PowerPoint
- Tableau, Jira, and Epicor knowledge preferred
- Must be bilingual in English
- Occasional travel to US and Malaysia facilities required