Quality Auditor Salary at Caremore BETA

Unitek Technical Services provides supplier management, development, and related technical services to corporations around the world. Disclaimer: This posting will re-direct you to Unitek Career page and submitting your application will take up to 5 minutes. Should you want to skip the step, please feel free to reach us or send your resume directly to eric.joyner@ntslabs.com Job Description: Aerospace Quality Auditor We are currently seeking an Aerospace Quality Auditor to support a full-time role traveling to various supplier locations. Auditors will audit suppliers to industry standard QMS to AS9100 specifications. The auditors will schedule and complete the audits in accordance with defined AR standard work and follow up and drive corrective action for all findings. We are willing to accept candidates located anywhere within 50 miles of Los Angeles, CA to support various supplier sites in Southern California, and occasional out-of-state sites as needed. Travel package will be offere

Job Summary: This position will be an integral part of our organization that is responsible for the development of medical technology and innovative, world-class products that save people’s lives. The Quality Manager is responsible for leading the corporate product quality systems, including setting corporate quality goals, managing and improving all aspects of the quality system, product quality, and documentation requirements for advanced electronic medical devices. Duties & Responsibilities: Defines, develops, and implements quality system procedures, work instructions, and forms. Must work with limited supervision and will be involved in and have input to project planning. Proficient in clearly communicating directions and in influencing people in adopting the best solutions, tools, working practices and promotes cooperation in defining an excellent technical product. Initiates and performs internal and supplier audits Works in collaboration with R&D Engineers and executes the qual

Job Description D'Leon Consulting Engineers is seeking a Quality Manager in Los Angeles, CA. Responsibilities Manage all QA/QC aspects of the project, ensuring compliance with quality standards and regulations. Develop, implement, and improve quality management systems, policies, and procedures. Establish measurable quality goals that align with project and client requirements. Define key performance indicators (KPIs) and monitor progress. Track and analyze quality metrics, identifying trends, risks, and issues. Provide regular reports on quality performance and corrective actions. Lead initiatives to optimize quality processes and resolve non-conformities. Implement best practices and innovative solutions to improve quality. Work with project teams, engineers, and contractors to address quality issues. Develop and deliver quality training for staff. Ensure adherence to health, safety, and environmental standards. Maintain accurate quality documentation and ensure compliance with audit

Responsibilities: Audit, monitor, evaluate, report and improve supplier quality system performance and provide technical support to suppliers Perform supplier evaluations including on-site audits to assess supplier capabilities, determine approval status, and verify corrective action Collect and add supplier information required for the Approved Supplier List Conduct component and product quality testing for purposes of supplier and component qualification and improvement Identify and implement statistical engineering tools and techniques to evaluate supplier process capability and technical performance Evaluate supplier quality systems, strategies, and regulatory compliance via vendor audits Collect and analyze quality metrics relating to Supplier Quality Identify and define correction actions and follow-up to ensure completeness and effectiveness Communicate supplier quality risks to upper management while suggesting improvements and cost savings where possible Qualifications: Educat

Specific technology/software: Solidworks/Creo (CAD software) Minitab Excel Must haves: Problem solving CAD/drafting skills Technical writing Nice to have skills: Statistical analysis Excel macro coding Power BI Job Summary: This person will be responsible for supplier quality audits, vendor management, and maintaining supplier quality metrics. Will work in a fast paced and dynamic environment where taking initiative and collaborating cross-functionally are critical for success. This role will work in close partnership with Quality, R&D, Operations, Sourcing, and RA. How you will make an impact: Audit, monitor, evaluate, report and improve supplier quality system performance and provide technical support to suppliers Perform supplier evaluations including on-site audits to assess supplier capabilities, determine approval status, and verify corrective action Collect and add supplier information required for the Approved Supplier List Conduct component and product quality testing for purp

Supplier Quality Engineer Duration - 1 Year, Contract, W-2 Location - Irvine, CA Pay - $35- $41.03 an hour Duties: * Responsible for supplier quality audits, vendor management, and maintaining supplier quality metrics. * Provide receiving inspection floor support, perform test method development, run supplier meetings, and design/risk document creation. * Work in close partnership with Quality, R&D, Operations, Sourcing, and RA. * Audit, monitor, evaluate, report and improve supplier quality system performance and provide technical support to suppliers * Perform supplier evaluations including on-site audits to assess supplier capabilities, determine approval status, and verify corrective action * Collect and add supplier information required for the Approved Supplier List * Conduct component and product quality testing for purposes of supplier and component qualification and improvement * Identify and implement statistical engineering tools and techniques to evaluate supplier process c

Job Summary: Quality Assurance Engineer will actively lead the improvement of customer satisfaction by leading the reduction of internal non-conformances and the elimination of customer returns through the effective utilization of continuous improvement techniques. This individual will also assist in the development of quality engineering and assurance personnel through effective mentoring and skill development programs. Primary Responsibilities: • Uses advanced Quality, Six Sigma methods and actively work with the production departments to effectively reduce non-conformance(s) and prevent returns. • Responsible for developing an effective corrective and preventative program that will concentrate its efforts on reducing scrap and rework. • Assists with operator and inspector training development requirements. • Mentors and assists with quality engineering development requirements. • Facilitates and processes customer returns through the material review process. • Conducts internal audi

OVERVIEW We are currently searching for a skilled professional to join a well-known client's team as a Quality Compliance Auditor in Los Angeles, CA. The Quality Compliance Auditor role will perform routine GMP audits as well as specialty and technical audits in relation to current products and prospective in-license agreements, provide compliance guidance and support throughout the Quality organization, and lead multi-departmental teams and initiatives. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES •To ensure success as a Quality Auditor, the candidate should possess in-depth knowledge of product standards and extensive experience as a related pharmaceutical experience preferably in manufacturing, quality assurance, or cGxP auditing and demonstrated project management experience in leading cross-functional teams. •Prepare and execute internal self-inspections and supplier audits an