Manager, Quality Salary at Triderma BETA

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

Description Title: Site Quality Manager Department: Business Planning & Operations Location: Project-Based Rotation Supervisor: Associate Director of Quality FLSA Status: Exempt Position Status: Permanent, Full-time Work Status: Hybrid SITE QUALITY MANAGER Hanwha Qcells USA Corp (Qcells USA), headquartered in Irvine, CA, specializes in providing utility-scale modules, solar photovoltaic (PV), and battery energy storage systems (BESS) project development, along with Engineering, Procurement, and Construction (EPC) services for solar and BESS projects nationwide. Qcells USA delivers comprehensive turnkey solutions encompassing the entire utility-scale project lifecycle. By choosing Qcells USA for turnkey solutions, customers can reduce uncertainty and risk, leading to enhanced investment returns and contributing to a more sustainable future. Qcells USA's complete turnkey solutions seamlessly integrate the expertise of our Development, Module, and EPC teams, while ensuring close coordinat

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

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

**Please note that this is an "onsite" role, and the successful candidate will be expected to work from our corporate Irvine, CA campus. Imagine how your ideas and expertise can change a patient's life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You'll bring your passion for problem solving and partner with various teams to influence decision-making for a product's entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology. As a Quality Manager, you will play a pivotal role in ensuring the highest standards of quality across our operations. You will be responsible for planning and directing assigned operational and improvement activities, managing a team of supervisors and associates, and driving continuous improvement initiatives. Your leadership will be crucial in maint