Teams at The Goodkind Co.

Supervise daily QA operations, lead QA personnel, coordinate quality workflows, review batch records and SOPs, support deviations/NCRs/CAPA/change control, lead investigations, support validation/calibration, audits, and cross-functional quality activities to ensure GMP and regulatory compliance.

Review and approve batch records and COAs, evaluate manufacturing and quality data, manage deviations/NCRs/CAPA and change control, perform root cause analysis and risk-based decision-making, support audits and continuous improvement to ensure GMP compliance and product release readiness.

Drive quality system improvements through data analysis, root cause investigations, CAPA implementation, validation support, risk assessments, and cross-functional collaboration to improve process capability and QMS effectiveness in a regulated manufacturing environment.