This is Cellares
Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.
Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.
•
Under supervision of scientists, the candidate is expected to provide hands-on support to small-scale and scale-up experiments and overall development of the Cellares advanced cell therapy manufacturing platform
•
Support cell line maintenance and leukopak processing, including isolation, activation, gene modification, expansion and cryopreservation
•
Contribute to high-quality technical documents, procedures, reports
•
Contribute to analysis and presentation of technical results at departmental meetings
•
Support technology characterization experiments informing internal equipment and consumables performance evaluation
•
Perform routine laboratory activities including ordering and equipment qualification/maintenance
•
BS/MS or equivalent in Bioengineering, Chemical Engineering, Biology, Biochemistry, or related field
•
0-4 years of process development or cGMP manufacturing experience in the cell therapy or bioprocessing field
•
Hands-on experience in aseptic technique; experience in primary immune cell culture or bioreactors preferred
•
Hands-on experience with semi-automated instruments for cell therapy manufacturing
•
Strong problem-solving skills and attention to detail
•
Strong technical writing skills and experience authoring SOPs and reports
•
Creative, self-motivated, eager to take on a wide variety of tasks and grow with evolving technology
•
Self-awareness, integrity, authenticity, and a growth mindset