Key Responsibilities: Lead and manage a team of up to three direct reports
Oversee a project portfolio comprising up to four small-scale projects
Organize laboratory activities in alignment with established guidelines and SOPs
Develop, optimize, and implement analytical methods for various applications
Lead the documentation and review of method development, validation, and implementation
Lead laboratory investigations to address product/process issues, deviations, CAPA, and complaints
Proven expertise in analytical method development, validation, and implementation (with a focus on HPLC)
Strong understanding of GMP, GLP, GDP, and regulatory requirements for drug development
Excellent leadership, organizational, and communication skills
Experience in managing cross-functional projects and collaborating with external partners
Familiarity with regulatory submissions and health authority interactions
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