Quality Associate - Princeton

+The Quality Associate is responsible for supporting quality operations by receiving and inspecting samples, · conducting routine visual inspections, and maintaining accurate tracking and documentation using Microsoft Office tools. · +Receive and log samples from various sites in ...

Support GMP manufacturing and quality systems to ensure compliance with FDA regulations and cGMP standards.Review and approve batch records and GMP documentation. · Ensure cGMP and FDA compliance. · Perform in-process and final inspections. · ...

A leading consumer packaged goods manufacturer seeks an Associate Quality Engineer to join its Contract Manufacturing Quality organization. · ...

Support GMP manufacturing and quality systems to ensure compliance with FDA regulations and cGMP standards. · Review and approve batch records and GMP documentation. · Ensure cGMP and FDA compliance. · Perform in-process and final inspections. · ...

The Quality Assurance Specialist is responsible for batch certification review of site QA activities related to manufacturing and packaging records. · ...

+The Quality Assurance Specialist is responsible for the batch certification review of site QA activities related to manufacturing and packaging records,+ · +Ensure compliance with Standard Operating Procedures (SOPs), equipment and instrument maintenance, calibration, qualificat ...

The Quality Assurance Specialist is responsible for the batch certification review of site QA activities related to manufacturing and packaging records, as well as all supporting documentation. This includes ensuring compliance with Standard Operating Procedures (SOPs), equipment ...

The Associate Director RBQM HOCT ICN will develop Quality Narrative at study level documenting end-to-end risk based quality management for critical data processes vendors demonstrating effective risk issue management. · Develop Quality Narrative at study level documenting end-to ...

The Associate Director Global Product Quality - Biologics directs quality oversight of clinical and commercial products at CMOs under contract by Otsuka ensuring compliance with regulatory expectations. · Directs quality oversight of GMP contract manufacturers. · Develops compreh ...

The Associate Director Clinical Quality Management serves as the central Risk-Based Quality Management Lead for Clinical Operations responsible for enterprise-wide proactive risk management across clinical trials. · This role owns the end-to-end RBQM framework including risk iden ...

This is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams.You'll have challenging work with meaningful impact. · We offer a wid ...

The Associate Director serves as the central Risk-Based Quality Management (RBQM) Lead for Clinical Operations responsible for enterprise-wide proactive risk management across clinical trials. · ...

The Associate Director Clinical Quality Management serves as the central Risk-Based Quality Management Lead for Clinical Operations responsible for enterprise-wide proactive risk management across clinical trials. · ...

The Associate Director External Data Quality Management is a strategic leadership role supporting high-quality execution of Genmab's clinical trial portfolio. · Portfolio and Strategic Leadership · Serve as a portfolio-level lead for external data quality and clinical data-relate ...

The Associate Director serves as the central Risk-Based Quality Management (RBQM) Lead for Clinical Operations responsible for enterprise-wide proactive risk management across clinical trials. · ...

· Quality assurance associate to join our team. · ...

We are seeking a talented and motivated Quality Assurance Associate. In this role, you will be responsible for performing field QA activities: in process checks in the aseptic processing area · AQL inspection for finished products retention sampling for finished products batch re ...

+Eugia is a US-based independent specialty pharmaceutical company focused on generic sterile injectables, oncology, hormones, · and ophthalmic medicines. · +Prepare Review Finalize SOPs MAPPs Internal Guidelines review Checklist supervise PVG function Eugias products · Coordinate ...

We are seeking a talented and motivated Quality Assurance Associate. In this role, you will be responsible forperforming field QA activities: in process checks in the aseptic processing area, approval for area clearance, AQL inspection for finished products, · Regular and predict ...

Location: Princeton, NJ onsite · About Summit · Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in buildin ...