6170 - Batch Disposition Associate / Quality Specialist - Durham, NC

The Quality Specialist is responsible for all Quality related functions that directly support Durham within the CDS2 Facility (COVID Drug Substance Vaccine Manufacturing) IPT (Integrated Product Team) while actively participating in and embracing an empowered team culture.We offe ...

We believe everyone has an opportunity to lead. We see the importance of your perspective and your ability to create value. · We want you to fit in—with an inclusive culture, focus on work-life fit and well-being, and a supportive, connected environment; but we also want you to s ...

The Quality Control Specialist is an entry-level opportunity within the Quality Control organization at AskBio. This individual will perform routine GMP testing activities in a regulated gene therapy manufacturing environment. · Perform routine analytical testing including but no ...

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.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 ...

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 ...

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 ...

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... · ...

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 ...

+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. · + · ++ · ...

Summary · The Specialist, Quality Control Microbiology, assists and supports the organization with initial compliance and ongoing preparation, testing and monitoring of conformance to established quality processes and standards for manufacturing and production. · The Specialist, ...

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. · ...

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 ...

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 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 Quality Control Microbiology assists in compliance preparation testing monitoring of conformance to established quality processes and standards. · The role performs Environmental Monitoring Microbiological testing data review report writing. · ...

Summary · The Specialist, Quality Control Microbiology, assists and supports the organization with initial compliance and ongoing preparation, testing and monitoring of conformance to established quality processes and standards for manufacturing and production. · The Specialist, ...

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 ...