Quality Engineer I or II

SMC Ltd.•Santa Rosa, CA

5h•$75,000 - $100,000•Onsite

About The Position

In the role of a Quality Engineer you will be responsible for deliverables to support SMC’s quality system. Evaluate and recommend opportunities for improvements in key measurement areas (customer complaints, scrap, cost of quality, PPM Internal/External). Provide customer support including the extended enterprise (suppliers) targeting permanent problem resolution and implementation of proactive preventative measures to prevent recurrence. Production support of sustaining programs will include maintaining inspection methods, troubleshooting support for quality inspectors, and data analysis. This position is expected to perform other related duties in conjunction with other employees and departments contributing to the overall team effort, efficient process, and safe working environment. This position includes many essential components necessary for successful and efficient manufacturing, and as such, shares full responsibility for the final product delivered to the customer. Performance will be based on execution of work, ability to meet projected timeline and production support requirements, ability to maintain expected levels of quality and control, communication, continual improvement, the ability to work in a team environment, and successfully coordinate the operations of multiple departments to achieve success.

Requirements

A Bachelor of Science degree in Engineering or similar technical discipline preferred.
Excellent planning, leadership, and client relationship skills
Excellent interpersonal communication and writing skills
ASQ, CQT/CQE
CMM/MicroVu Programming Experience
Solidworks Modeling Software Experience
Gage R&R, CpK/PpK studies,
IQ, OQ, PQ validation/qualifications, DoE analysis… etc.
Various metrology equipment.
Microsoft Office suite
Statistical process control

Nice To Haves

Injection molding background
Medical Device manufacturer background
Experience using Minitab Software for SPC, DOE, etc.
Communication, Oral - Ability to communicate effectively with others verbally.
Communication, Written - Ability to communicate in writing clearly and concisely.
Detail Oriented - Ability to pay attention to the minute details of a project or task.
Time Management - Ability to utilize the available time to organize and complete work within given deadlines.
Working Under Pressure - Ability to complete assigned tasks under stressful situations.
Reliability - The trait of being dependable and trustworthy.
Previous high-volume manufacturing experience.
Experience within the medical device industry.
Previous experience with lean manufacturing concepts.

Responsibilities

Lead new product launches with Measurement System Analysis (MSA), tolerance and GD&T reviews, FMEA, control plans, FAI and DOE input.
Identification of critical variables and attributes.
First article sampling and reporting.
Develops Inspection Instructions/Techniques.
Statistical analysis if required.
SPC dimensional monitoring for production.
Preparation for quality assurance of initial trial and subsequent production.
Prepare Validation Quote Analysis as needed.
Provide technical support to Program Management Department.
Oversee DMR (Device Master Records) control for all new product launches.
Work with Program Managers to write and implement Engineering Change Orders.
Identifies opportunities for improvement to process and product.
Provides applicable training.
Utilizes the NCR systems to facilitate improvements.
Assist in corrective action (CAPA) process in accordance with relevant ISO requirements.
Quality Planning, Non-Conforming Materials, Continuous Improvement, Weekly Meetings, Corrective/Preventive Actions, Audit Activities, etc.
Supports the ISO 13485 Business Management System through Internal Auditing.
Assist with third party and FDA quality audits as needed.
Provide expertise in the Quality Assurance area on new projects and prepare written reports and documentation for internal and/or external use as required or assigned.
Coordinates implementation of product and process improvements.
Conducts investigation, root cause analysis and corrective actions.
Monitors and expedites the closure of corrective/preventive actions resulting from customer complaints, safety issues, management review, non-conforming product and staff generated.
Participates and Leads Lean Projects for waste elimination.
Develops, maintains and updates Procedures, Work Instructions, and Forms.
Responsible for following documented procedures established by the SMC Ltd. Quality Management System while adhering to all company policies, work environment and safety requirements.