Manager, Quality Salary at American Metal Bearing Co BETA

Job Description Job Description Salary Range: $87,500 to $95,000 Annually Summary: Under the direct supervision of the Quality Management/Risk Management Director, the Quality Management/Risk Management Manager is responsible for providing management support to the Agency’s Quality Management/ Risk Management Program, to include The Joint Commission Ambulatory Program, The Joint Commission Patient-Centered Medical Home Certification, Quality Management Trainings, Quality Management surveys, clinical risk management program, QM/RM staff supervision, and other related projects as assigned, and prepares Quality Management/Risk Management narrative and data reports. DUTIES AND RESPONSIBILITIES: Responsible for providing support for the effective management of the Quality Management/ Risk Management Program in accordance with Agency policy and standards, and provides recommendations for continuous improvement, and supervises QM/RM staff as assigned Responsible for managing the Agency’s The

POSITION SUMMARY: The Quality Manager at Irvine, will work to apply knowledge in the implementation of an integrated Quality Management System (QMS) to ensure full compliance and a continual product, process, and supplier improvement culture. This individual will work closely with all cross-functional teams to create quality strategies that support customer needs and overall business objectives. Work on and provide solutions to a wide range of difficult problems relating to the quality aspects of design, validation, and manufacture of medical devices. The Quality Manager serves as owner and administrator of several aspects of the quality system, including but not limited to supplier management, customer feedback, process control, internal audits, change management, and design control. This quality and compliance professional will be responsible for assuring conformance to product serve as the sites lead ISO Representative. ESSENTIAL JOB FUNCTIONS: Plans, implements, and directs quality

SUMMARY: Primarily responsible for maintaining, measuring, and evaluating the effectiveness of the quality management system to assure products and services meet or exceed VSE Aviation quality standards, customer requirements, and applicable legal or regulatory requirements. DUTIES & RESPONSIBILITIES: Responsibilities include, but are not limited to: Accountable for leading annual internal and 3rd party audits. Ensures QMS processes are established, implemented, and properly maintained, including the oversight and control of all documents and data related to the requirements of the QMS system. Manages quality metrics, trends and activities to improve cost, quality, and customer satisfaction. Develops written quality plans by conducting analyses, identifying critical control points, and implementing preventive measures and verification procedures. Accountable for assessing Customer Satisfaction by conducting an annual customer satisfaction survey and overseeing customer complaints and p

Project Details 6-Month contract. (Extension/Conversion likely). On-site, 5 days per week. (40 hours). Key Responsibilities: Oversee core quality functions: CAPA, change control, audits, training, and complaints. Manage and develop quality team members. Act as the Quality Management Representative, reporting on QMS performance and promoting regulatory awareness. Ensure audit readiness and lead interactions with regulatory bodies. Maintain and improve quality procedures and documentation. Qualifications: 5+ years of quality experience in medical devices. Strong understanding of ISO 13485, 21 CFR Part 820, ISO 14971; MDSAP and MDR knowledge a plus. Experienced in eQMS tools and audit processes. ISO 13485 Lead Auditor certification required; ASQ certifications preferred.

Position Summary This position will lead quality control operations, ensuring compliance with industry regulations and high product standards. Reporting to senior leadership, this role oversees Microbiology, Analytical Chemistry, Quality Control, Inspection, Quality Assurance, and Validation while collaborating cross-functionally to support production and distribution. Key Responsibilities Oversee QC teams and ensure lab operations align with regulatory and business goals. Maintain and improve quality systems, SOPs, and compliance processes. Conduct internal audits, manage third-party lab testing, and oversee regulatory inspections. Handle customer complaints, product recalls, and compliance documentation. Manage employee training programs and continuous improvement initiatives. Regular international travel required. Qualifications Bachelor's degree in Chemistry or related field. 10+ years of QC/QA experience 5+ years in leadership roles with FDA audit experience. Strong knowledge of i

Job Description Job Description SUMMARY: Manages the development and implementation of the Quality Engineering function to ensure that VACCO Space Products and Services meet specifications and contractual agreements. ESSENTIAL DUTIES AND RESPONSIBILITIES: Maintain a high level of communication and credibility with DCMA, Customer Representatives, Regulatory Agencies and other external quality personnel. Recommend Quality Management System changes to the Director of Quality or his designee when changes are required by industry, contract requirements or audit findings. Support audits by Space customers, government, and regulatory agencies and reports the results to the Director of Quality or his designee for necessary action. Submit information to the Director of Quality or his designee in order to update action items to conform to the results of internal and customer audits. Implement all necessary corrective actions requirements by results of Internal or customer audits. Implement requi

**Job Description Summary** Reporting to the Associate Director, Unit Quality WW IPD, the Senior Manager - Quality Engineering provides direct management and technical support to the Quality Engineers supporting the WW IPD Design Center. The position shall provide quality engineering leadership, oversight, and direction in problem-solving and team-building capabilities. The position is also responsible for sustaining a QMS that complies with applicable standards and regulations, consistent with Corporate and Business Unit policies and procedures. The position shall support new product development and product maintenance through the application of Quality engineering skills for medical devices, assuring that all BD products are designed utilizing systems which comply with applicable regulatory standards and conform to customer expectations for safety and effectiveness. **Job Description** We are **the makers of possible** BD is one of the largest global medical technology companies in t

About SCAN SCAN Group is a not-for-profit organization dedicated to tackling the most pressing issues facing older adults in the United States. SCAN Group is the sole corporate member of SCAN Health Plan, one of the nation's leading not-for-profit Medicare Advantage plans, serving more than 277,000 members in California, Arizona, Nevada, Texas and New Mexico. SCAN has been a mission-driven organization dedicated to keeping seniors healthy and independent for more than 45 years and is known throughout the healthcare industry and nationally as a leading expert in senior healthcare. SCAN employees are a group of talented, passionate professionals who are committed to supporting older adults on their aging journey, while also innovating healthcare for seniors everywhere. Employees are provided in-depth training and access to state-of-the-art tools necessary to do their jobs, as well as development and growth opportunities. SCAN takes great pride in recognizing our team members as experts i