The Executive Director, CMC Quality Assurance will lead and build a QA team, ensuring global compliance for drug and device development. Responsibilities include overseeing event processes, supplier audits, supporting regulatory submissions, and driving continuous quality improvements, requiring extensive experience in biotech QA.

The Senior Manager will lead analytical development for biologics, ensuring successful strategies for method development, validation, and stability testing, while collaborating with internal and external teams.

The Associate Director, Data Review ensures data integrity for clinical trials, oversees data review processes, collaborates with cross-functional teams, and mentors junior members.

The Senior Manager, Accounting will oversee accounting functions, manage monthly book closing, assist with SEC reporting, audit preparation, and financial statement preparation.

As a CMC Project Manager, support CMC activities, manage sample processes, coordinate teams, maintain timelines, and communicate project updates to stakeholders.