This role invites individuals to join a talent community, enabling them to explore future career opportunities and stay informed about industry trends. Membership helps pave the way for potential future roles with Blueprint Medicines.

Manage GxP training, procedural document control, and oversee document management systems. Ensure compliance with GxP standards and regulatory agencies. Responsible for training curricula and metrics reporting.

Lead in-vivo pharmacology strategies, oversee drug candidate characterization, and collaborate on discovery projects while managing research activities and reporting results.

The role supports GxP training, quality systems, compliance, and global inspection logistics, coordinating document preparation and compliance across various quality functions.

The Senior Director, Corporate Legal Affairs will provide legal advice on SEC compliance, governance, and capital markets in a biopharmaceutical setting, collaborating across teams to manage documentation, reporting, and regulatory adherence.

As Associate Architect in IT, you'll lead infrastructure projects, troubleshoot systems, mentor colleagues, and optimize cloud solutions within a growing biopharmaceutical company.

Manage compensation programs by supporting analysis, design, execution, and communication to ensure they are competitive and effective, partnering with employees and leaders.