Search the 9 jobs at Tessera Therapeutics

As a Manufacturing Associate, you will execute clinical GMP manufacturing operations, manage projects, ensure product quality, and adhere to documentation practices. Responsibilities include executing master batch records and collaborating with cross-functional teams in a fast-paced environment.

The Executive Assistant will support high-level executives by coordinating meetings, managing communications, organizing travel plans, and driving projects. This role requires exceptional organization, attention to detail, and strong interpersonal skills. The assistant will be proactive in managing diverse tasks and collaborating with teams in a fast-paced startup environment.

The Senior Specialist in Quality Control will perform analytical assays, support GMP laboratory operations, review QC data from method qualifications, and assist in documenting experiments. This role requires strong leadership and multitasking abilities within QC lab operations to ensure compliance and readiness for drug substance testing.

The VP of Portfolio, Programs and Alliance Management (PPAM) is responsible for setting the strategy for managing programs and alliances, improving PPAM capabilities, leading governance forums, and driving program development. This role includes monitoring risks, resolving resource challenges, and promoting effective communication within teams to align with enterprise goals.

The Executive Director/Vice President will lead two Program teams focused on genome editing therapies, guiding them from early development to registration. Responsibilities include providing strategic leadership, ensuring alignment across development teams, managing program budgets, and fostering collaboration and innovation while maintaining clear communication with stakeholders.

The Senior Engineer I/II in Computational Biology will design and develop databases for storing large volumes of data, develop computational biology pipelines using cloud technologies, and collaborate with various teams to integrate solutions for research in clinical investigations. The role requires strong programming skills and a solid understanding of data management in a fast-paced environment.

The Head of Clinical Operations will oversee global clinical trials, manage vendor relationships, and ensure compliance with FDA and GCP guidelines. Responsibilities include strategic planning for clinical studies, patient recruitment, regulatory submissions, and leading the clinical operations team to achieve corporate goals.

The Executive Director, Regulatory Science (CMC) will lead the development of regulatory strategies for biopharmaceutical products, oversee regulatory submissions, manage a regulatory CMC team, and engage with regulatory agencies to resolve issues and refine strategies, ensuring compliance with global regulations.

Seeking a Senior Manufacturing Associate with 3-5 years of industry experience in GMP manufacturing. Responsibilities include leading and executing manufacturing activities, ensuring product quality, and adherence to GMP procedures. Must have experience in authoring batch documentation and collaborating with cross-functional teams.