Chemist

• Perform analytical tasks to qualify standards and ensure reference materials are available for cGMP analytical testing
• Support Research and Development, Quality Control, Manufacturing, and external clients
• Support the Stability Program, including study initiation, pull scheduling, packaging, labeling, analytical testing, and data compilation
• Run routine and non-routine tests on samples, including stability studies and standard characterization/qualification testing
• Perform equipment calibration, titrant standardization, stability chamber monitoring, and preventative maintenance
• Troubleshoot analytical instruments and techniques in the QC laboratory
• Identify and communicate problems and solutions related to processes, procedures, and materials
• Investigate anomalous test results and take corrective action
• Maintain laboratory cleanliness and organization in accordance with safety, regulatory, chemical hygiene, and cGMP policies
• Maintain daily records in SAP and LIMS, update material statuses, and initiate incident reports
• Manage hazardous and non-hazardous waste
• Participate in Quality, R&D, and cross-functional team meetings
• Package stability samples and standard materials using appropriate verified materials
• Author technical documents, including Standards and Stability Program protocols and reports
• Perform critical and time-sensitive testing, including high-potency materials and difficult methods
• Support laboratory investigations and assist in determining root cause
• Conduct thorough data review according to good documentation practices
• Work independently without frequent supervisory oversight

Explore Standards and Stability Analytical Chemist at Corden Pharma - A Full-Service CDMO. Review requirements and application details.