· Apply established statistical methods to support development, qualification, and validation of bioanalytical methods (e.g., potency assays, ddPCR workflows)
· Perform statistical analyses for assay validation, including linearity, accuracy, precision, and detection limits
· Support stability studies through trend analysis, control charting, and regression modeling
· Assist in data review, interpretation, and troubleshooting for assay development and optimization activities
· Contribute to statistical analysis plans (SAPs), validation protocols, technical reports, and regulatory documentation
· Collaborate with cross-functional teams (QC, Analytical Development, Process Development, Regulatory)
· Support investigations, deviations, and root cause analyses with statistical input
· Assist in developing and maintaining data trending and reporting tools
· Ensure compliance with regulatory requirements (e.g., ICH, USP, FDA)
· Communicate statistical findings clearly to stakeholders