Quality Assurance Specialist - Durham

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 ...

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. · ...

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 ...

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 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 QA Contractor 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... · ...

We are looking for a Lead Specialist to join our Quality Assurance team. In this role you will make a real difference by supporting quality management system and requirements for deviations CAPAs Change Controls Lab Investigation OOs and Method Validations. · ...

The Senior Quality Assurance Specialist is accountable for driving results in a fast-paced environment by effectively performing activities as directed to ensure quality and compliance with applicable regulatory requirements and internal procedures. · ...

We are seeking a Quality Assurance Specialist II to provide quality assurance oversight in sterile pharmaceutical manufacturing. · Support site readiness for regulatory inspections and compliance with industry standards · Review and approve records, protocols, and deviations to e ...

+Provide Quality Assurance oversight for sterile pharmaceutical manufacturing and support assessment and preparation of manufacturing sites for Pre-Approval inspections by regulatory agencies for new products. · + · ++ · ...

We are seeking a Senior Specialist Quality Assurance to join our team. The ideal candidate will have a minimum of 5 years experience in quality assurance oversight of sterile manufacturing, sterile process validation and/or sterile process technology transfer. · ...

We are looking for a Quality Assurance Senior Specialist to join our Quality team in Durham. The successful candidate will be responsible for overseeing all Facilities operations within an FDA-approved clinical cGMP manufacturing facility and advancing our mission. · Act as subje ...

The Specialist, NC Product Quality Assurance (PQA) will be responsible for supporting Quality's oversight of laboratory and manufacturing operations at Beam's manufacturing facility in RTP, North Carolina. The role will provide Quality oversight of routine manufacturing, testing, ...

The Specialist, NC Product Quality Assurance (PQA) will be responsible for supporting Quality's oversight of laboratory and manufacturing operations at Beam's manufacturing facility in RTP, North Carolina. · The role will provide Quality oversight of routine manufacturing, testin ...

The Specialist NC Product Quality Assurance PQA will be responsible for supporting Qualities oversight of laboratory and manufacturing operations at Beams manufacturing facility in RTP North Carolina. · This role will provide Quality oversight of routine manufacturing testing and ...

Quality Assurance professional with a BS Biology, Microbiology, Pharmacy, Chemistry or Chemical Engineering and at least 5 years experience in the Pharmaceutical Industry. · Quality Assurance professional with a BS Biology, Microbiology, Pharmacy, Chemistry or Chemical Engineerin ...

The Validations Contractor – GMP Quality Assurance will assist in the management of Quality Management System (QMS) and support Culture of Quality. · Work alongside department customers on development, implementation, and integration of Equipment and Computer Systems Validation p ...

The Validations Contractor – GMP Quality Assurance will be responsible for assisting in the management of Quality Management System (QMS) and will strongly support Culture of Quality. · ...

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 ...