Employment Type: Full-time Available Positions: 1 Location : On-Site Application Deadline: Dec 22, 2025 Summary The LCMS Principal Scientist will be responsible for supporting non-GLP, GLP (non-clinical), and GCLP (clinical) projects. The role is responsible for supporting lab operations in a non-GLP area. Key Activities Independently conduct LC-MS method development for biologics (e.g., ADC, mAb, protein, peptide, oligonucleotide, etc.) in support of developability assessment, comparability assessment, in-depth characterisation, biotransformation, and CQA-related analysis. Present and interpret data internally and/or externally as needed. Serve as Subject Matter Expert (SME) for the LCMS platform. Serve as the Principal Investigator responsible for interaction with the client from the study design to scheduling, conducting, reporting, and transferring data. Ensure responsiveness to the client, timely delivery, and overall customer satisfaction. Provide oversight of the laboratory, mentor junior staff, and collaborate to keep improving operational excellence. Assist in establishing and improving policies, procedures, work instructions and SOPs. Understand and adhere to corporate standards regarding code of conduct and Environmental Health however, due to the large volume of resumes received only those candidates selected for an interview will be contacted. Please attached your resume to your application. Job ID: 8083
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