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Lead analytical method development, validation, and QC activities for small molecules. Collaborate with cross-functional teams and manage external partners to support drug development and regulatory submissions.

The Principal Scientist will optimize purification processes for mAbs, coordinate with CDMO partners, and oversee compliance and documentation for regulatory submissions.

The Executive Director, Investor Relations will manage investor relations and corporate communications, ensuring effective communication with investors and analysts, drafting core materials, and coordinating multiple stakeholders.

Lead global market access strategies for oncology products, ensuring readiness for launches by aligning regulatory, pricing, and reimbursement pathways across key markets, especially in Europe.