Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We're developing a mammalian synthetic biology platform--from cells to software--to enable the design and manufacture of next-generation therapeutics.

The (Associate) Director, Technology Transfer will play a pivotal role in delivering biologics cell line development (CLD) campaigns for our customers and successfully transferring Asimov processes (CLD and upstream process) into our customers' laboratories and manufacturing facilities. This role involves building and nurturing long-term, mutually beneficial relationships with pharmaceutical and biotech companies, technology providers, academic institutions, and other strategic partners.

About the Role:

Provide expert technical guidance on tech-out evaluation design, CLD planning, scale-up, optimization, and troubleshooting for various biopharmaceutical manufacturing processes (e.g., mammalian cell culture, purification, analytical methods, and viral vector production). Work cross-functionally with internal departments (CLD, DNASC, Process Development, Analytical Development, Quality, Facilities, Business Development) to ensure project success. Oversee the preparation and review of critical documentation, including tech transfer plans, protocols, CLD reports, cell history documentation, and drug master filings. Develop and implement standardized tech transfer procedures, protocols, and best practices. Work with functional leads and teams to drive the implementation of new technologies and innovative approaches to enhance tech transfer efficiency and capability. Support customer inspections, audits, and related site visits at our site in Boston. Represent the company at industry conferences, networking events, and in discussions with potential partners. Stay abreast of industry developments, emerging technologies, and competitive dynamics to inform company strategy. Collaborate closely with Business Development to assess new project opportunities and provide technical expertise. This role is expected to involve up to 20% travel, primarily to customer sites and conferences. About You: Advanced degree (MSc or PhD) in a relevant scientific or engineering discipline (e.g., Biochemical Engineering, Chemical Engineering, Biotechnology, Biochemistry, Biology). Minimum of 10 years of experience in the biopharmaceutical or life sciences industry, with at least 5 years specifically in cell line development. Additional experience in areas such as technology transfer, process development, or manufacturing sciences within a CDMO or pharmaceutical/biotech company is a plus. Direct experience in a CDMO environment is highly preferred, including customer-facing interactions or proven experience transferring technology between independent sites. Strong leadership, communication, interpersonal, and presentation skills. Excellent project management abilities, with a proven capacity to manage timelines, budgets, and resources effectively. Knowledge of cGMP, FDA, EMA, and ICH guidelines. Strong analytical, problem-solving, and decision-making skills. Ability to work effectively in a fast-paced, dynamic, and collaborative environment. Demonstrated ability to build and maintain strong working relationships with clients and internal stakeholders. Strategic thinker with a proactive and results-oriented approach.

We're fueled by a vision to transform biological engineering into a fully-fledged engineering discipline. Should you join our team, you will grow with a constantly evolving organization and push the frontiers of synthetic biology. Company culture is key to Asimov, and ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives.