Perform a wide range of analyses primarily method development and validation of projects within, but not limited to, molecular biology areas of Biopharmaceutical Services. Meet TAT for assigned testing/projects and work independently.
Review and evaluate raw data for acceptability. Assist other technical staff in evaluation of raw data for acceptability.
Set up and validate new analytical or related processes used by the department. Lead a project through completion of the project. Be able to plan and organize work week and communicate schedule to management when required. Attend client facing meetings as needed.
Document work as required for GMP compliance. Work with quality departments to ensure all documentation meets GMP requirements for each assay developed.
Troubleshoot method and instrumentation problems; be proactive in solving technical problems.
Train technical staff and perform internal data review as need arises.