The Senior Manager, GMP Quality Assurance at Nuvalent is responsible for ensuring quality compliance in drug substances and products, overseeing contract manufacturers, conducting audits, managing quality agreements, and representing the QA department in projects. They will review documentation, conduct risk assessments, and ensure adherence to cGMP practices throughout the CMC lifecycle.

The Counsel, Legal Affairs will provide legal support for precommercial and commercial needs, draft and review commercial contracts, assist with SEC filings and corporate governance matters, and ensure compliance with legal regulations in the pharmaceutical industry.