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Root cause analysis (RCA) and CAPA implementation for project topics, and general lab topic. Investigation and management of deviations, as Lead Investigator. Quality oversight and audit readiness in GMP-regulated labs (participation in audits for
You will identify compliance gaps, guide investigations, and lead improvements that support reliable laboratory processes. You will also share your expertise and help teams prepare for regulatory inspections. Lead improvement projects with QC, Quality
Provide technical leadership and mentorship to a diverse team with expertise in pharmaceutical formulation, process development, scale-up, and manufacturing support for synthetics drug products. Lead, develop, and inspire a multidisciplinary Drug Product
You will act as the Technical Subject Matter Expert (SME) for Single-Pill Combinations (SPCs). You will be responsible for the technical oversight of manufacturing processes across internal sites and external partners (CMOs), ensuring that complex
This role will be pivotal in ensuring all products manufactured meet the standards required for marketed drug products. They will be accountable for defining contamination control strategy and its sterility assurance practices and sever as a subject