Specialist, Product Quality Assurance - Durham, NC

The position will support the Quality team to ensure that the design history files meet all corporate policies and government regulations for Design Controls. · ...

We are looking for an intern who can start work in March with an anticipated length of around 5-6 months. · Assist in the transfer of raw electronic data directly from laboratory equipment into secure, validated systems and/or the electronic archive. · Ensure that archived files ...

Participate in the roll-out/support of a new Lean Systems Development Lifecycle (SDLC) and Quality Management System (QMS). Create procedures or revise existing ones where needed. · ...

We are looking for an intern who can start work in March with an anticipated length of around 5-6 months. · The Quality Assurance Intern (Archive) will support the Quality Assurance team by helping organize, transfer and maintain electronic and paper laboratory records. · ...

We are looking for an intern who can start work in March with an anticipated length of around 5-6 months. · The Quality Assurance Intern (Archive) will support the Quality Assurance team by helping organize, transfer, and maintain electronic and paper laboratory records. · This r ...

We are looking for an intern who can start work in March with an anticipated length of around 5-6 months. · The Quality Assurance Intern (Archive) will support the Quality Assurance team by helping organize, transfer and maintain electronic and paper laboratory records.Assist in ...

This position will assure corporate compliance with applicable GMP national, international, and state regulations. · Manage assigned day-to-day QA responsibilities in support of the company's Product Quality systems. · Provide timely support for Third Party Deviations, Third Part ...

We are seeking an experienced Quality Assurance Lead (QA Lead) to drive quality strategy, testing execution and continuous improvement across complex software products. · Lead and oversee QA activities across the full software development lifecycle (SDLC) · Define implement and c ...

The QA Contractor GMP Quality Assurance will assure corporate compliance with applicable regulations. This role will be based at the headquarters facility in RTP NC with domestic travel expected. · Bachelor s degree in a scientific field and 2+ years of experience in GMP based Qu ...

The QA Contractor will assure corporate compliance with applicable GMP national, international and state regulations. The role will be based at our headquarters facility in RTP NC with domestic travel expected. · Manage assigned day-to-day QA responsibilities in support of the co ...

The Specialist, Quality Assurance is responsible for performance of Batch Record Review and Disposition function for LCI. · Responsible for performing and managing activities related to GMP document review and disposition of commercial products. · Act as primary point of contact ...

The Specialist, · Quality Assurance is responsible for performance of Batch Record Review and Disposition function · for LCI.Within that function, · assure compliance with laws and regulations and in a manner consistent with best practices · and applicable guidance. · ...

The Specialist, Quality Assurance is responsible for performance of Batch Record Review and Disposition function for LCI.Within that function, assure compliance with laws and regulations and in a manner consistent with best practices and applicable guidance. · ...

+We're hiring a Quality Assurance Specialist to support a pharmaceutical manufacturing site in Durham, NC. · +Own and manage change controls end-to-end... · ...

The Quality Assurance Manager (eQMS & EU GDP) will be responsible for two distinct but complementary quality functions at Cavalier Logistics: (1) the implementation and ongoing management of the Electronic Quality Management System (eQMS), and (2) the implementation and managemen ...

The Quality Assurance Engineer is responsible for the design, construction, validation, · maintenance and overall compliance of facilities, systems and processes at Novartis Gene Therapies in Durham. · ...

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 ...

The Specialist, Quality Assurance is responsible for performance of Batch Record Review and Disposition function for LCI. · Review and approve Master Batch Records.Perform the review of records and determine disposition of Medical Devices,Packaged/Labeled Medical Devices,Clinical ...

We are seeking a Quality Assurance Engineer to join our team and ensure the reliability and performance of refurbished GPUs and servers. · Conduct incoming, in-process, and final inspections on refurbished GPUs and servers to verify compliance with quality standards. · Perform fu ...

The Quality Assurance Engineer is responsible for the design, construction, validation, maintenance and overall compliance of facilities, · systems and processes at Novartis Gene Therapies. · Provides QE support for clinical and commercial gene therapy products. · Support of all ...

We are leaders in plasma-derived medicines and transfusion medicine and develop produce and market innovative medicines solutions and services in more than 110 countries and regions. We are seeking a Clinical Quality Assurance Specialist to join our team who will participate in t ...