Manager, Quality Salary at Ingedata BETA

Triple Ring Technologies, Inc. offers a unique environment for talented individuals interested in undertaking varied technical challenges, primarily in medical device and life science industries. Headquartered in Newark, CA, we are an innovative research and development company that partners with clients to deliver complex technical solutions. Our highly interdisciplinary team includes senior professionals from industry, finance, and academia, with extensive experience in medical device, life science, clean tech, security, and industrial technologies. We rely upon each other for technical excellence, real-world engineering and commercial wisdom. Learn more at www.tripleringtech.com. Job Summary The Manager of Quality Assurance will maintain and lead the implementation of Triple Ring's Quality Management System (QMS) for client projects. He/she will work collaboratively with project leadership and other team members to develop, coordinate, and own the QMS elements of a project. These wi

Job Details Job Location AAON Tulsa - Tulsa, OK Position Type Full Time Salary Range $89458.00 - $121031.00 Salary Job Shift Day Job Category QA - Quality Control Description Job Summary: The Quality Manager is responsible for site level Quality Management System compliance and improvement opportunities to ensure our products meet customer and engineering specifications. This role involves leading Quality Assurance initiatives, managing quality teams, and developing strategies to improve overall product quality assurance and manufacturing efficiency. The Quality Manager drives multiple cross functional teams, collaborates across departments, and works with other locations to promote and evolve the AAON quality culture. Essential Job Duties and Responsibilities: Establish and maintain site level quality standards and records based on Global QMS. Leads and mentors the Tulsa quality assurance team, providing training, guidance, and support to ensure effective performance. Oversees Quality

The Nuclear Company is the fastest growing startup in the nuclear and energy space creating a never before seen fleet-scale approach to building nuclear reactors. Through its design-once, build-many approach and coalition building across communities, regulators, and financial stakeholders, The Nuclear Company is committed to delivering safe and reliable electricity at the lowest cost, while catalyzing the nuclear industry toward rapid development in America and globally. #LI-IG1 About the role: The Manager of Quality Assurance (QA) is a critical role responsible for ensuring all aspects of the company's operations adhere to the highest quality standards and regulatory requirements within the nuclear energy industry. This position requires a deep understanding of quality management systems, nuclear safety regulations, and best practices. The Manager of QA will implement and maintain a robust QA program, ensuring the safety, compliance of quality-related company activities. This role wil

Responsible for performing responsibilities as assigned to effectively support implementation of the Quality Management System. Will provide global quality oversight for customer complaint management and associated root cause analysis (RCA), corrective and preventive action (CAPA) management, and documentation. Required to support the functions in achieving compliance to quality and animal health standards, company policies and procedures, as well as all applicable regulatory requirements. This role will strive to create a positive and mutually beneficial relationship between Inotiv, its employees and its customers, contributing to achieving the growth of Inotiv RMS business. This is a remote position with occasional travel required. Serves as an administrator of Inotiv's Quality Management System software and provides user support, training and mentoring Monitors the lifecycle of complaint entry, investigations and CAPAs to closure and collaboratively works with other functional depar

Job Description Job Description SUMMARY: The Manager of Quality ensures that all materials, processes, and procedures meet regulatory and quality standards and promptly resolves any issues or discrepancies that may arise. ESSENTIAL DUTIES AND RESPONSIBILITIES: Customer Single Point of Contact Disposition customer complaints and issue RMAs Coordinate the completion of customer corrective actions and responses Participate in customer audits Manage internal quality system (ISO 9001) for all Hussey Copper locations Ensure compliance with regulations Lead Internal Audits process Manage and coach corrective actions Own Change Management process Document management and reviews Work with EHS to implement Integrated Management System to include Safety and Environmental Lead continuous improvement for quality and systems functions Implement and be process owner for new Management System Software Gensuite Lead software implementation for multiple sites Maintain all modules once implemented (Actio

Akron Bio is continuing to transform and further its rapidly growing capabilities and is now seeking highly motivated professionals to join our expanding team. This is an exciting opportunity to play a critical role within our organization that is driving advanced therapy development and commercialization with high quality industrial scale solutions. We manufacture and distribute components and raw materials for cell therapy discovery, development, and commercialization to meet industry needs worldwide. We offer an array of highly competitive benefits and perks to our valued associates. Responsibilities: Responsible for the development, implementation and maintenance of the Quality Management System (QMS) and periodically provides reports on the performance of the QMS along with recommendations for improvement. Develops and maintains a current Quality Manual System Manual and current Standard Operating Procedures (SOPs), guidelines, standards and records. Responsible for controlling ne

Description Responsible for the maintenance, execution and monitory of Vista Packaging and Logistics Columbus, Ohio facility Quality Management (QMS) Good Distribution Practices (GDP) and compliance with all local state and federal (FDA) as well as all corporate policies and procedures. Acts as primary contact for all local, state and federal regulatory agencies pertaining to the QMS scope. Conducts/coordinates required Quality, Security and Regulatory assessments. Supports development of QMS components (i.e., Quality, Security and Regulatory training.) Responsible for oversight and maintenance of Corrective and Preventive action program. Responsible for oversight of the change control process, risk management and cGMP refresher training. Lead and manage a QA Team to successfully deliver the project to the required quality standards. Assure Quality procedures are developed, maintained, and practiced delivering customer's satisfactions. Work with Customer Service Representatives Communi

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting Job Description Join Thermo Fisher Scientific for impactful work, innovative thinking, and a customer-focused culture. Location/Division Specific Information At Lenexa, you will be a key member of the Quality leadership team supporting manufacturing of in vitro diagnostics and laboratory reference materials. As QC manager, you'll contribute to a leadership team focused on ensuring our customers receive the products needed to achieve their scientific goals. Discover Impactful Work: Lead a team in overseeing, testing, and evaluating products to meet industry standards and customer needs. A day in the Life: Lead the Quality Control team under the Director of Quality, managing raw materials, product testing, and process improvement in two labs. Help redesign the vision for the QC team based on our evolving business while maintaining laboratory budget to plan. Understand Customer needs and Operational requirements