BioPharma Consulting JAD Group
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Biotech • Pharmaceutical
Leads investigations into deviations, nonconformances, and quality events; performs root cause analysis, develops and monitors CAPA plans, prepares compliant technical reports, and collaborates with Operations, Quality Assurance, Engineering, Maintenance, and other teams. Ensures investigations meet GMP, regulatory, and internal quality standards while maintaining accurate, traceable documentation and facilitating cross-functional problem-solving.
