Director, Quality Systems - Trumbull, CT, United States

This position may require 10-20% domestic and/or foreign travel. · ...

The Director of Quality Systems holds significant influence over Cooper Surgical's quality standards and regulatory compliance. · ...

The Quality Systems Engineer is a key member of the Quality Assurance unit responsible for leading and enhancing quality system activities including quality event investigations protocol writing risk assessments and CAPAs. · Lead and author complex quality event investigations pr ...

+The Quality Systems Engineer is a key member of the Quality Assurance unit responsible for leading and enhancing quality system activities including but not limited to quality event investigations protocol writing risk assessments and CAPAs. · +• Lead author complex quality even ...

The Quality Systems Engineer is a key member of the Quality Assurance unit responsible for leading and enhancing quality system activitiesLead and author complex quality event investigations protocols risk assessments and CAPAs. · ...

Provides oversight for the development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies. · ...

The Planet Group of Companies is seeking a Quality Systems Specialist to oversee the development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies and established standards. · Provides oversight for the development and mai ...

Maintain and update Quality Assurance documentation in support of the ISO 9001:2015 Quality Management System. · ...

As a Quality Assurance Specialist , you will maintain and update Quality Assurance documentation in support of the ISO 9001:2015 Quality Management System. · You will be instrumental in supporting the execution and continuous improvement of the company's Quality Management System ...

Lead initiatives to maintain and improve the Quality Management System (QMS) in compliance with FDA Quality Systems Regulations (QSR), ISO 13485, EU MDR, and other applicable regulations. · Develop, implement, and maintain quality processes. · Suport internal and external audits. ...

Maintain and update Quality Assurance documentation in support of the ISO 9001:2015 Quality Management System. · ...

The Internal Audit Program Coordinator supports and maintains the global internal audit program for a medical device organization operating under ISO 13485, · FDA 21 CFR Part 820/QMSR, · MDSAP, · and EU MDR requirements. · ...

The Supplier Quality Engineer II is responsible for leading SCAR SCN and Supplier Nonconformance processes. · ...

As a Staff Software Engineer on the CooperSurgical R&D Software Development team you will have a critical role in developing maintaining enhancing and supporting our customer-facing software products as well as internal applications. · ...

The Senior Medical Writer is responsible for developing high-quality clinical and regulatory documents that support compliance and product lifecycle needs for global standards such as EU MDR and FDA regulations. · ResponsibilitiesAuthor and edit clinical documents including Clini ...

The Quality Control Inspector is responsible for performing routine inspections of components, · subassemblies, and finished products to ensure compliance with approved drawings, · specifications, inspection plans, and regulatory requirements.This role supports product quality, · ...

To be part of our organization every employee should understand and share in the YNHHS Vision support our Mission and live our Values. · ...

To be part of our organization, every employee should understand and share in the YNHHS Vision, support our Mission, and live our Values. At Bridgeport Hospital, we are committed to providing quality medical care and treatment that is coordinated and centered on the patient's spe ...

To be part of our organization every employee should understand and share in the YNHHS Vision support our Mission and live our Values. · Performs high quality PET CT imaging procedures utilizing appropriate age specific standards to obtain the desired diagnostic patient informati ...

The Operations Manager will play a critical role in establishing and operating Pelham's new manufacturing facility in Connecticut. This includes project managing the site setup from build to validation and staffing. · ...