Principal Scientist LCMS

Overview

The LCMS Principal Scientist will be responsible for supporting non-GLP, GLP (non‑clinical), and GCLP (clinical) projects, supporting lab operations in a non‑GLP area.

• Independently conduct LC‑MS method development for biologics (e.g., ADC, mAb, protein, peptide, oligonucleotide, etc.) in support of develop ability 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 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 & Safety (EHS).
• Perform other related duties as assigned.

• Supervisory experience in both project and talent (people) management is preferred.
• Ability to work independently and pay close attention to details.

• PhD, M.S., in Chemistry, Biochemistry or related scientific fields required, including a minimum of 4+ (Ph.D.) or 9+ (Master’s) years of CRO/Pharma/Biotech experience.
• Hands‑on experience with high‑resolution LCMS method development and in‑depth characterization.

TQR is an equal‑opportunity employer that encourages diversity. We will consider all applications.

Accommodation for applicants with disabilities is available upon request.