
51 - 200 funcionários
Fundada em 2017
🧬 Biotecnologia
💊 Farmacêutico
🤖 Inteligência Artificial
Biotechnology • Pharmaceuticals • Artificial Intelligence
A Asimov é uma empresa de biologia sintética que oferece uma plataforma integrada, combinando células hospedeiras GMP engenheiradas, bibliotecas de partes genéticas validadas, construção de DNA, serviços de laboratório e software de design baseado em nuvem para acelerar o desenvolvimento e a fabricação de biológicos, terapias genéticas e celulares. A empresa utiliza modelos orientados por dados e IA para projetar, simular e otimizar sistemas genéticos e oferece tanto ferramentas para o desenvolvimento interno quanto desenvolvimento completo de linhagens celulares e processos a partir de seu laboratório em Boston. A Asimov faz parcerias com clientes de biotecnologia e farmacêuticas para fornecer bancos de células produtoras clonais, DNA e documentação regulatória, visando simplificar o desenvolvimento terapêutico e a fabricação escalável.
🕒 Abril 12
🗣️🇺🇸🇬🇧 Inglês obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

51 - 200 funcionários
Fundada em 2017
🧬 Biotecnologia
💊 Farmacêutico
🤖 Inteligência Artificial
Biotechnology • Pharmaceuticals • Artificial Intelligence
A Asimov é uma empresa de biologia sintética que oferece uma plataforma integrada, combinando células hospedeiras GMP engenheiradas, bibliotecas de partes genéticas validadas, construção de DNA, serviços de laboratório e software de design baseado em nuvem para acelerar o desenvolvimento e a fabricação de biológicos, terapias genéticas e celulares. A empresa utiliza modelos orientados por dados e IA para projetar, simular e otimizar sistemas genéticos e oferece tanto ferramentas para o desenvolvimento interno quanto desenvolvimento completo de linhagens celulares e processos a partir de seu laboratório em Boston. A Asimov faz parcerias com clientes de biotecnologia e farmacêuticas para fornecer bancos de células produtoras clonais, DNA e documentação regulatória, visando simplificar o desenvolvimento terapêutico e a fabricação escalável.
• 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, DNA Assembly, 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 the efficiency and capabilities of tech transfer. • Occasionally support other programs within the Strategic Alliance team's purview, such as CHO Edge or RNA Edge portfolio projects. • 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 approximately 20% travel, primarily to customer sites and our Boston headquarters.
• Advanced degree (MSc or PhD) in a relevant scientific or engineering discipline (e.g., Biochemical Engineering, Chemical Engineering, Biotechnology, Biochemistry, Biology) • Minimum of 10-12 years of experience in the biopharmaceutical or life sciences industry, with at least 1-3 years in a leadership role focused on cell line development, technology transfer, process development, or manufacturing sciences within a CDMO or pharmaceutical/biotech company. • Deep technical expertise in the genetic medicines field, specifically viral vector (AAV and LVV) with demonstrated experience leading tech transfers and effectively communicating complex technical data. • Strong understanding of the CHO biologics space including cell line development, process development, and comparative manufacturing constraints. • 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.
• stock options • eligibility for 401(k) plan • annual career development stipend • medical, dental, vision, life and disability insurances • flexible time-off • unlimited sick time
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