Teams at The Ritedose Corporation

Lead QA oversight for manufacturing process monitoring, process control, and investigations to ensure cGMP and regulatory compliance. Manage and mentor QA staff, lead complex investigations and root cause analyses, approve GMP system changes, participate in audits, drive continuous improvement, and maintain effective quality systems across pharmaceutical manufacturing and distribution.

The Bulk Operations Technician maintains and troubleshoots manufacturing equipment, performs preventive maintenance, documents work, and supports emergency maintenance in a cleanroom environment.

Perform cGMP-compliant QA activities including batch record review, verification of critical processing steps, QMS and controlled document review, issuance of Certificates of Analysis/Conformance, trend/process improvements, and product complaint reviews.