Key Responsibilities:
Develop, validate, and execute analytical methods (HPLC, LC/MS, GC, GC/MS, ICP‑MS, ELISA, MSD) to support client drug substance and drug product programs.
Perform sample analysis for small and/or large molecules across multiple phases of development under strict regulatory timelines.
Independently author, review, and execute SOPs, methods, validation protocols, and final client reports in compliance with GMP/GLP requirements.
Critically review raw data for accuracy, integrity, and regulatory compliance with moderate to minimal supervision.
Maintain, troubleshoot, and perform minor repairs on analytical instrumentation to support uninterrupted project execution.
Coordinate consumables, reagents, and equipment needs to meet client timelines and project budgets.
Ensure laboratory readiness, safety, and inspection preparedness for regulatory and client audits.
Stay current with analytical chemistry advancements and contribute to continuous impr...