QA Batch Record Review Specialist

Global Compliance Partners (GCP) is a GxP and GMP compliance consulting firm with over a decade of experience supporting biopharma and cell & gene therapy organizations. We partner with leading drug developers and manufacturers to deliver validation, quality, and compliance solutions, from QC, QA, CSV/CQV and process validation through tech transfer and BLA

Global Compliance Partners (GCP) is a GxP and GMP compliance consulting firm with over a decade of experience supporting biopharma and cell & gene therapy organizations. We partner with leading drug developers and manufacturers to deliver validation, quality, and compliance solutions, from QC, QA, CSV/CQV and process validation through tech transfer and BLA...

Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Quality Assurance Specialist to support our Batch Record Review activities within Manufacturing. In this role, the Quality Assurance Specialist Performs activities in support of dispositioning products...

Curia in Rensselaer, NY is seeking a QA Dispositioner Specialist to ensure quality disposition of incoming materials, intermediates, and APIs at the site with relocation assistance. The role reviews batch records and supporting documentation to guarantee GMP compliance and proper disposition.Requirements include a Bachelor's in Life Science and at least 5...

Role QA Specialist supporting drug product manufacturing at Regeneron’s Rensselaer facility, focusing on start‑up, validation, and ongoing quality assurance of formulation, filling, inspection, and packaging operations. Responsibilities develop/review SOPs, perform on‑floor quality reviews, support audits/inspections, manage quarantine and line...

Regeneron Pharmaceuticals, Inc. seeks a Senior Quality Assurance Specialist to lead on-floor activities supporting dispositioning of product and/or raw materials, ensuring cGMP and QA policy compliance.The role includes deviation/CC/CAPA handling, investigations, and document reviews with external partners. The successful candidate will train and mentor...

Regeneron Pharmaceuticals, Inc. in New York is seeking a Senior QA Validation Specialist (Shipping) to validate and qualify equipment, systems and processes in compliance with regulatory requirements and company standards supporting manufacturing and distribution. You will execute validation protocols, review data, investigate deviations and coordinate with...

Curia in Rensselaer, NY seeks a Quality Disposition Supervisor to lead the batch disposition process, review batch records, and ensure compliant closure of Deviations, CAPAs, Change Controls, and investigations. The role supervises the disposition team and interfaces with cross-functional groups to meet supply commitments.The ideal candidate has a minimum of...

RoleQA Specialist supporting drug product manufacturing at Regeneron’s Rensselaer facility, focusing on start‑up, validation, and ongoing quality assurance of formulation, filling, inspection, and packaging operations.Responsibilitiesdevelop/review SOPs, perform on‑floor quality reviews, support audits/inspections, manage