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Responsible for issuing clinical and commercial in-process and final product labels for labeling operations.

Functional responsibilities include performing in process and drug product label printing activities; ensuring accurate and timely issuance of labels for manufacturing and packaging labeling activities for Cell Therapy Development and Operations (CTDO). Responsible for issuing clinical and commer...

Participate in resident care and Quality Assurance/Quality Improvement (QA/QI) meetings. Act as a liaison with local public health departments for reporting infectious diseases. Company perks and employee recognition programs.

The Director, Quality Assurance – GxP (GCP) is responsible for managing GxP Quality Assurance (QA) functions with an emphasis on Good Clinical Practice (GCP), compliance for both clinical and marketed products. The Director, Quality Assurance – GxP (GCP) ensures adherence to relevant regulatory

Define and document data governance rules, data quality metrics, and stewardship models Support data profiling and data mapping activities between source systems and MDM hub Validate. Work closely with data architects, developers, and QA teams to support the design and delivery of MDM solutions. ...

Represent the Risk Management unit at various project meetings and provide quality input in the resolution of quality-related issues. Must have GMP, Quality, and in-depth risk management knowledge. Develops and Maintains Quality Metrics to monitor compliance.

The primary focus of the QA Specialist role will be to support routine clinical and commercial production to ensure consistent compliance with regulatory and industry expectations. Review executed batch records to ensure compliance with approved procedures and communicate and resolve discrepancie...

The Quality Assurance Label Control (QALC) Labeling Specialist supports the cGMP Label Control operations for the client site, including the coordination, issuance, reconciliation, and management of production labels and records. Minimum of 1 year of relevant labeling experience in a cGMP/FDA reg...

Job Title: QA Automation Engineer .Location: Iselin, NJ (194 Wood Ave S).Work Schedule: Hybrid – Onsite Monday to Wednesday (3 days/week).Contract Duration: 12 months (with potential for extension or conversion).We are seeking a skilled QA Automation Engineer to join our Capital Markets Risk T

Responsible for issuing clinical and commercial in-process and final product labels for labeling operations.