The Senior Scientist I will innovate and implement synthetic biology workflows, collaborate on protein screening, and analyze complex biological datasets.

The Associate Director of TMF Management oversees the Trial Master File processes, ensuring compliance and operational efficiency in clinical development, while leading SOP development and TMF governance.

The Senior Scientist II will develop and scale high-throughput DNA assembly processes, collaborate across teams, and lead innovative synthetic biology efforts.

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 of Program & Alliance Management leads program and alliance teams, fostering collaboration across departments to enhance biotherapeutic development and decision-making.

The Vice President, Global Respiratory Products Leader will lead late-stage respiratory programs, develop teams, strategize, and ensure compliance with regulations in respiratory medicine.

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.

The Senior Manager will coordinate cross-functional Research operations, manage outsourced production logistics, and drive technology onboarding while collaborating with multiple teams and improving operational workflows.

The Associate Director of Pharmacovigilance will oversee global case processing, manage vendor oversight, ensure compliance, and support safety reporting for clinical programs.

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

The Associate Director will oversee QC for biologics, manage external testing partners, develop analytical methods, and ensure compliance with regulatory standards.

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.

Coordinate the hiring process by managing interview scheduling, candidate communications, and providing support to the P&C team with administrative tasks.