The Associate Director/Director will act as a strategic IT liaison for Quality and Regulatory departments, lead GxP compliance initiatives, oversee development systems selection, and enhance collaboration across teams to align IT with business objectives, driving accountability and support for development activities.

The Manager, External Quality Control at Verve oversees Quality Control activities at contract manufacturers and CROs, ensuring compliance with cGMP standards. This role includes managing QC operations, laboratory investigations, data review, method validations, and coordinating testing of gene-editing products. Strong technical and compliance experience in a biotechnology or pharmaceutical setting is essential.

The Associate Director/Director will enhance SOX compliance and IT governance by designing policies, managing audits, and collaborating with G&A teams. Responsible for data governance, mentoring teams, and implementing controls to safeguard data integrity while driving strategic initiatives with senior management.

The Associate Director of Preclinical Pharmacology will lead a team in conducting and interpreting preclinical pharmacology studies for gene editing therapeutics. Responsibilities include designing in vivo studies, collaborating with cross-functional teams, managing CRO relationships, and contributing to IND submissions.

As a Senior Engineer/Associate Principal Engineer, you will develop, scale-up, and support the manufacturing of novel gene therapies. Responsibilities include leading lab studies, refining process controls, managing GMP manufacturing campaigns, and mentoring junior team members.

Lead all aspects of GMP quality assurance at Verve, including developing and implementing a quality management system, oversight of GMP production and testing, vendor quality management, and QA laboratory operations. Manage the QA team, establish SOPs and compliance standards, and collaborate with other departments on quality-related issues.