Batch Records Jobs

Lead and develop upstream manufacturing operations and staff at Amgen’s West Greenwich facility to ensure safe, compliant, and efficient execution of the production plan.

Lead Synthego's GMP quality programs as a hands-on Quality Assurance Manager overseeing eQMS, CAPA, deviation management, audits, and team development to ensure product and process compliance.

Kincell Bio seeks a detail-oriented Manufacturing Specialist to support on-site cGMP cell therapy production, operate automated and manual equipment, and manage GMP documentation and corrective actions.

Lead a 1st-shift manufacturing team at Alcami's Morrisville site to maintain cGMP-compliant sterile drug product operations and drive quality and performance.

Experienced QA Specialist needed to perform cGMP document reviews, batch and lab data release, audits, and investigations for Lonza's Tampa manufacturing site on the 3–11 PM shift.

FUJIFILM seeks a Manufacturing Specialist 1 to act as a process SME and support batch planning, documentation, and continuous improvement in a 24/7 cGMP manufacturing environment.

Trove Brands is hiring a Senior Quality Specialist to lead QMS development and ensure regulatory, analytical, and product quality from R&D through commercialization for sports nutrition and consumer products.

Provide QA support for sterile CT parenteral drug product filling and facility commissioning at Eli Lilly's Indianapolis manufacturing site.