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The VP, Head of Quality will establish global quality strategies, oversee compliance, develop quality systems, and lead the Quality organization to support clinical trials and regulatory requirements.

The Director will lead Technical Program Management, optimizing processes for the ML and wet lab platform to enhance drug discovery.

The Director, Safety Science manages pharmacovigilance activities, interprets safety data, and oversees safety reporting processes in clinical development.

The Executive Director will lead and scale the pharmacovigilance organization, ensuring compliance and safety throughout drug development while collaborating cross-functionally and mentoring a high-performing team.

The Vice President, Global Respiratory Products Leader oversees late-stage respiratory programs, manages a team of medical monitors and clinical scientists, develops ambitious development plans, and collaborates with cross-functional leaders to ensure success in clinical trials for asthma and COPD.

Generate:Biomedicines invites interested candidates to submit resumes for potential future openings in machine learning and biological engineering.

Lead GxP quality strategy and operations for development-stage programs, ensuring regulatory compliance and effective quality systems across GCP, GLP, and GMP activities.

Lead Late-Stage Biology and Preclinical Development at Generate:Biomedicines. Oversee diverse teams, guide drug discovery, mentor future leaders, and drive AI-driven therapeutic innovations.

The Associate Director will lead product management for a research informatics platform, aligning cross-functional teams and driving innovative solutions in therapeutics development.

The Director, Product Management will lead the development of a Machine Learning platform for novel therapeutics, defining product strategies and collaborating with cross-functional teams.