Supplier Quality and QMS Specialist - Mebane

As Supplier Quality and QMS Specialist,you will be responsible for sustaining and improving the quality of products being delivered by our suppliers. · Coordinate and drive supplier and part qualifications; · Track and monitor scorecards of supplier performances. · ...

At ABB, we help industries outrun - leaner and cleaner. Here, progress is an expectation - for you, your team, and the world. As a global market leader, we'll give you what you need to make it happen. It won't always be easy, growing takes grit. But at ABB, you'll never run alone ...

DEPARTMENT: Quality · LOCATION: Durham, NC, Onsite/Not Remote · COMPANY: Humacyte Inc (Nasdaq: HUMA) is developing a disruptive biotechnology platform to deliver universally implantable bioengineered human tissues, advanced tissue constructs, and organ systems designed to improve ...

Join a Legacy of Innovation · The SAP Specialist - Quality Management is responsible for evaluating, conceptualizing, and implementing new requirements from the business division. · ...

The SAP Specialist - Quality Management is responsible for evaluating, conceptualizing and implementing new requirements from the business division. · ...

We are seeking a QA Consultant to support quality assurance activities within the pharmaceutical and oncology sectors. · The successful candidate will play a key role in ensuring adherence to quality standards and regulatory requirements while collaborating with cross-functional ...

We are working to change the trajectory of cancer mortality by detecting cancer early when it can be cured. · ...

The Quality Audit Specialist is responsible for supporting the development, · implementation and maintenance of the internal audit program. · Create annual internal audit schedules, · develop internal audit plans and coordinate activities · with cross-functional teams. · ...

We are working to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative technologies that can transform cancer care.The Quality Audit Specialist is responsible for supporting the development implementation and maintenance of the internal au ...

Support the development and implementation of the internal audit program and other quality management activities.Auditor for internal audits to ensure compliance with procedures and regulatory standards. · ...

The QA Contractor will assure corporate compliance with GMP national and international regulations. · Manage assigned day-to-day QA responsibilities in support of the company's Product Quality systems. · Provide timely support for Third Party Deviations and Vendor Management acti ...

The Validations Contractor – GMP Quality Assurance will assist in managing AskBio's Quality Management System (QMS) and support its Culture of Quality. · ...

The Quality Audit Specialist will support the development implementation and maintenance of internal audit program responsible for creating annual internal audit schedules developing internal audit plans coordinating activities with cross-functional teams. · Responsible for creat ...

· Our mission is to detect cancer early, when it can be cured. We are working to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative, safe, and effective technologies that can transform cancer care. · We are a healthcare company, pioneer ...

The Quality Audit Specialist is responsible for supporting the development, implementation and maintenance of the internal audit program. · This role will also support other Quality Management Systems (QMS) activities as needed. · This role is based at our Durham, North Carolina ...

The Quality Audit Specialist is responsible for supporting the development, implementation and maintenance of the internal audit program. This role will also support other Quality Management Systems (QMS) activities as needed. · This role is based at our Durham, North Carolina of ...

The QA Contractor will assure corporate compliance with applicable GMP national, international, and state regulations. · ...

We are seeking a Quality Assurance Specialist with ISO 13485:2016 experience to help build implement and maintain a medical-device-aligned Quality Management System QMS. · Lead execute ISO 13485 QMS implementation certification readiness activities including gap assessments remed ...

The Validations Contractor – GMP Quality Assurance will be responsible for assisting in the management of AskBio's Quality Management System (QMS) and will strongly support AskBio's Culture of Quality. · Work alongside department customers on development, implementation, and inte ...

Process Alliance is a leading engineering consultancy firm dedicated to delivering innovative solutions in engineering automation manufacturing services and medical devices. · Own and manage change controls end-to-end from initiation through implementation and closure · Coordinat ...