Search the 11 jobs at Tessera Therapeutics

The Senior Specialist in Quality Control will perform analytical assays, support QC laboratory operations, review QC data, and assist with method lifecycle documentation for compliance with GMP standards in gene therapy products.

The Vice President, Head of Portfolio, Programs and Alliance Management at Tessera is responsible for establishing the vision and strategy for managing programs and alliances. This includes guiding program managers, improving tools and capabilities, facilitating governance, and monitoring program risks, with a focus on fostering communication and high-performance teams.

The Executive Director/Vice President of Program Leadership will establish vision and strategy for genome editing therapies, lead program teams, ensure alignment across the enterprise, manage budgets, and foster a culture of collaboration and innovation to drive program success from early development to registration.

Lead engineering efforts in the Computational Biology team to solve biological questions using cloud technologies. Develop databases, queries, and computational biology pipelines, collaborating closely with Data Engineering and Software Engineering teams. Document procedures and processes critical for research.

This role involves leading clinical operations for global trials, ensuring compliance with regulatory guidelines, managing CROs, developing clinical strategies, and achieving timelines and budget goals.

The Manufacturing Associate will execute clinical GMP manufacturing operations, manage on-the-floor activities, adhere to GMP procedures, and document processes. Responsibilities include authoring SOPs, managing cross-functional collaboration, and ensuring product quality through compliance with established guidelines.

The Executive Assistant will support high-level executives in a dynamic biotech startup, managing calendars, coordinating meetings, handling travel arrangements, and facilitating communication. This role requires exceptional organizational and interpersonal skills, attention to detail, and the ability to navigate a fast-paced environment.

The Senior Director will lead the Gene Rewriting discovery efforts at Tessera Therapeutics, overseeing preclinical development programs focused on genetic diseases, engineering therapeutic candidates, and managing a team of scientists. Responsibilities include collaboration with the platform team, developing disease models, and contributing to regulatory applications.

The Senior Director/Executive Director will lead oligonucleotide chemistry strategy, manage team execution, identify industry trends, and oversee external manufacturing processes for nucleic acid therapeutics, while ensuring compliance with regulatory requirements and building a robust team platform.

The Senior Manager/Associate Director, QA Operations will provide oversight and support for GMP manufacturing activities, reviewing and approving batch records, testing protocols, and related documentation. This role involves leading quality investigations, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to promote a safe and efficient work environment.

The Principal Engineer will develop innovative ML solutions for managing sparse, high-dimensional biological data, creating robust pipelines ensuring data traceability, and implementing best practices in MLOps. Responsibilities include optimizing ML models for resource-constrained environments and fostering collaboration across teams to communicate complex concepts.