Teams at KCAS Bio

Supports quality assurance for bioanalytical work by reviewing documents, data, protocols, and reports; conducting audits and inspections; reviewing deviations and investigations; maintaining QA records; assisting with SOP reviews, training, data trending, and continuous improvement. Collaborates with scientific and operational teams to ensure regulatory, procedural, and quality compliance while managing multiple priorities accurately and professionally.

Lead regulated bioanalytical studies from setup through reporting using LC-MS/MS and sample preparation workflows. Perform data review, troubleshoot assay and production issues, ensure GLP compliance and data integrity, communicate with clients, resolve audit findings with Quality Assurance, oversee study timelines, and train junior staff. Support audit readiness and regulatory inspections while serving as a technical and study lead.

Coordinates the preparation, review, formatting, validation, and finalization of scientific study reports for bioanalytical studies. Compiles report sections and data tables, identifies discrepancies, ensures compliance with protocols, SOPs, GLP requirements, and regulatory standards, tracks deadlines, maintains documentation, and collaborates with scientists and study teams. The role also supports templates, process improvements, reporting technology updates, and junior team members.