Quality Engineer I or II

Salary Range: $75,000.00 To $ Annually

Located in beautiful Santa Rosa, CA, SMC, Ltd. is a globally recognized premium supplier to the medical market with locations throughout the world. People committed to speed, technology, and exceptional performance are the cornerstone of our organization. Comprised of dedicated people and decades of manufacturing experience, we have continued to experience strong growth and currently have outstanding career opportunities for equally dedicated people.

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.

• Reviews new projects and sees to the following as applicable:
• 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;
• 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.
• Interfaces with customers:
  • 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…