• Develop, validate, and troubleshoot analytical methods for drug substances and drug products.
• Define analytical control strategies and implement methodologies throughout development stages.
• Collaborate closely with process development teams (drug substance and drug product).
• Manage all analytical activities at R&D labs.
• Lead and mentor junior analysts.

The ideal candidate must also have a strong background in organic impurities in drug substances and drug products, as well as experience in forced degradation studies, method validation and method transfer between laboratories.

Preferred Qualifications:

• Prior experience with the development and characterization of small molecules, peptides, or oligonucleotides.
• Familiarity with analytical techniques for immediate- and controlled-release oral solid dosage forms.
• Experience with LC-MS/MS systems and their application in trace-level impurity analysis or bioanalytical method development is highly desirable.