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**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 Precision Inc. manufactures medical devices and military electronics for some of the largest companies in Silicon Valley and Mexico.
We are constantly improving our operations and looking for new ways to meet our Customer's needs through continuous improvement.
**General Job Description**:The Supplier Quality Engineer is responsible for the management and development of the Key Suppliers.
This includes supplier quality system implementation, test and inspection plans (source inspection), supplier audits and risk management.
The Supplier Quality Engineer leads supplier development initiatives and is a technical resource for the materials, manufacturing, and quality departments with regards to product quality, supplier development and supplier process evaluation.
**Duties & Responsibilities**:- Participates in Supplier's Selection, Evaluation and Re-evaluation process.- Manages and/or performs source inspection, first article inspection process, product qualification including manufacturing process verification.- Works closely with the supplier to sustain and improve product quality.- Develops all necessary documents including but not limited to, product qualification plan, supplier quality requirements and expectations, etc.- Performs periodic supplier audit and risk assessment.- Performs failure analysis and corrective and preventive actions related to suppliers.- Prepares monthly reports of Supplier Quality and On Time Delivery for management review.- Establishes and runs/attends meetings with suppliers for Continuous Product / Process Improvements / Cost reduction.
**Education, Training & Experience**:- Bachelor's Degree in Engineering, Supply Chain or 5-10 years experience in related field.- Minimum of 5 years Supplier Management and Development experience in a manufacturing environment.- Previous experience with medical devices recommended.- Familiar with QA/QC systems, ISO 13485:2016 and 9001:2015 standard implementations that would include creating, reviewing, and revising operating procedures, work instructions, and the ECO process.- Experienced in metal Plating technologies e.G.
Anodizing, Chemical films, Zinc plating etc.
**Knowledge, Skills & Abilities**:- Knowledge of Quality Systems, ISO 13485:2016 and ISO 9001:2015.- Strong understanding of statistical control, PFMEA and risk management.- Ability to work independently and under pressure.- Ability to frequently travel locally and within US.- A solid technical background including expertise in electro-mechanical and mechanical assembly.- Must be strong in supplier quality management and possesses in-depth knowledge on modern quality techniques, such as six sigma and statistical quality control methodology