trackwise , SAP, Iso 13485, m-Learning, Documentum, Veeva Vault

Quality Assurance, GDPMDS, QMS processes, Iso 13485, EU IVDR, Regulatory Affairs, FDA QSR, Documentation control, Capa

quality assurance, healthcare quality standards, analytical problem-solving, report-writing, audits, Regulatory Requirements

batch records , Gxp, SAP, Sops, Iso 9001, OQ, Gmp, Root Cause Analysis, IQ, regulatory inspections, Capa, customer supplier complaints, validation training, continuous quality improvement, risk assessments, FSSC 22000, Internal Audits, training on quality standards, material and product release, quality systems management, PQ, Change Control, deviations, audit processes, supplier qualification processes, Regulatory Submissions, qualification and validation activities, external audits

SCAR, CCAR, Rohs, Pharma standards, Kosher Certification, GMP protocols, REACH, GDP, ISO 9001 standards

, Regulatory Compliance, Quality Frameworks, Auditing, Process Improvements, Documentation and Reporting