Director, Quality Salary at Mason Controls BETA

Quality Manager – Aerospace Contract Manufacturing Location: Burbank, Ca Reports To: Director of Quality About the Role: We are seeking a Quality Manager to lead quality assurance, compliance, and continuous improvement in our aerospace manufacturing operations. This role is critical in ensuring our products meet AS9100, ISO 9001, FAA regulations, and customer expectations. The ideal candidate has a strong background in electrical components, quality systems, root cause analysis, supplier quality, and continuous improvement methodologies. They must be a hands-on leader who fosters a culture of quality, accountability, and operational excellence. Key Responsibilities: Quality Assurance & Compliance; Continuous Improvement & Problem-Solving; Supplier & Customer Quality Management; Leadership & Team Development Maintain and oversee the Quality Management System (QMS) in compliance with AS9100, ISO 9001, and FAA regulations. Lead internal and external audits, ensuring adherence to aerospac

LISI AEROSPACE is ranked 60th in the global aerospace value chain and specializes in the design and manufacture of high-tech metal components to enhance aircraft safety and performance. Active since 1950 in the fastener market (no. 3 worldwide), LISI AEROSPACE has been a recognized player in metal components for aircraft engines and airframes since 2011. With its dedication to industrial excellence, LISI AEROSPACE aims to become a leader in costs, quality, deadlines and workplace safety. This mindset is represented at every level of our company and by all of our team members. At LISI AEROSPACE, we focus above all on advancement and flexibility. Every employee is empowered and has the latitude they need to carry out their assignments and develop their skills. We provide this mobility and training through our Corporate University, the LISI Knowledge Institute (LKI). As a result, our company is growing fast and always welcoming new talents. PRIMARY SUMMARY: This role plans, organizes, and

Overview: Monterey Park Hospital, located in the San Gabriel Valley of Los Angeles, is a 101 bed acute care community hospital providing our community with advanced medical and culturally sensitive healthcare services for over 50 years. Monterey Park Hospital is recruiting for a Quality Coordinator (non-clinical) in our Quality Assurance Department. This position reports to the Director of Quality/Risk Management. Responsibilities: The Quality Coordinator (non-clinical) assists the Director of Quality/Risk Management by supporting performance improvement (PI) and Risk Management activities by ensuring PI and Patient Safety Plans are updated annually, reviews policy and procedures, provides education to staff through hospital orientation, skills events, department staff meetings and annual reorientation, reviews occurrence reports timely, processes and documents accurately, abstracts quality data for OPPE evaluations, core measures, falls, risk events and clinical quality indicators for

Description Home Search Jobs Job Description QA Specialist II Contract: El Segundo, California, US Salary Range: 45.00 - 50.00 | Per Hour Job Code: 350996 End Date: 2025-05-06 Days Left: 15 days, 3 hours left Apply To discuss more about this job opportunity, please reach out to Chitrank Rastogi (LinkedIn URL - https://www.linkedin.com/in/chitrank-rastogi-55119a102/), email your updated resume at Email - chitrank.rastogi@collabera.com or give me a call at (425) 523-1648. Thank you! Pay Range - $45 to $50/hr. (negotiable) Job Description: Job Roles & Responsibilities: We are seeking a Senior Specialist of Quality Operations responsible for Product Disposition. This position will participate in Quality activities to ensure compliance with applicable quality objectives and regulatory requirements. This position is located at our El Segundo, CA site and report into the Associate Director of Quality Operations. Responsibilities: Perform Product Disposition and Lot Closure. Includes commercia

Job Title: Administration D (ADSD) Location: Canoga Park, CA (Onsite) Duration: 12 months on W2 Pay Rate: $25 to $29 per hour on W2 Job Description: SPPS support to VP of Operations, prepare weekly staff meeting agenda and weekly staff meeting agenda for SPPS president Travel Booking & Expense Reporting for VP of Operations, Sr. Director of Quality, Security, Advanced programs and support to other leaders. Special projects/events support, including event coordination, conference room set up, and catering. 10% - Other duties as assigned. Supply ordering for executive suites to include kitchen items Skills: Required Skills Must know Excel, PowerPoint, Word, Microsoft Office, SharePoint, and Concur experience Desired Skills: Travel Booking & Expense Reporting for VP of Operations, Sr. Director of Quality, and all of SPPS Leadership as needed. (this is a big part of the job) Special projects/events support, including event coordination for Executives on site, conference room set up, and ca

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

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

JOB SUMMARY: Assists the Director in maintaining and revising the Quality and Performance Improvement program, projects, and initiatives across the Hospital. Coordinates the activities of departments, committees, and medical staff to develop and document ongoing evaluation activities. Performs studies and problem-focused reviews; interprets data; develops and implements action plans; and monitors and evaluates performance. Promotes the Quality and Performance Improvement program to medical, nursing and support services. EXPERIENCE/QUALIFICATIONS: Basic Qualifications: Minimum five (5) years of experience as a licensed hospital nurse required. Minimum three (3) year of experience in quality-related activities such as Medical Staff Peer Review, Quality Management, Performance Improvement, or Patient Safety/Risk Management. Strong planning, interpersonal and conflict resolution skills. Effective communication skills including speaking, writing, listening, and facilitating. Able to receive