Manager, Quality Salary at Basf Se BETA

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

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

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Project Manager Quality and Compliance Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution. Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting

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

Who We Are Johns Manville is a leading manufacturer and marketer of premium-quality insulation and commercial roofing, along with glass fibers and nonwovens for commercial, industrial and residential applications. Our products are used in a wide variety of industries including building products, aerospace, automotive and transportation, filtration, commercial interiors, waterproofing and wind energy. A proud member of the Berkshire Hathaway family of companies, we serve customers in more than 80 countries around the globe. We are committed to delivering positive and powerful experiences, because we are successful only when our employees and customers thrive. We are passionate, we care about people, we perform at a superior level, and we protect others and our environments. Pay Range $109,400.00-$150,400.00 Annual This is the base salary pay range that an applicant can expect to make upon hire. Pay within this range will vary based upon relevant experience, skills, and education among o

Job Summary Senior Manager, Quality has primary responsibility for establishing and maintaining compliance of Kalila Medical’s (KMI) processes and procedures to the FDA (US) and PMDA(Japan) Quality System Regulations, and ISO 13485. This role will manage, lead and mentor the Kalila Medical Quality team. Senior Manager, Quality will manage and maintain compliance for quality systems as defined in the company’s Quality Manual including Management Oversight, Supplier Controls, Equipment Controls, Nonconformance Management, CAPA, Complaint Handling and Adverse Event Reporting, Corrections and Removals, Document Control, Lot Release, Training, Production & Process Control, Design Controls/Assurance, Risk Management etc. Senior Manager, Quality will manage the collection, analysis, maintenance and presentation of quality data/metrics to monitor and assure the overall suitability and effectiveness of KMI’s Quality System. Shall develop and implement strategies and supporting initiatives to pr

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