Position Summary Cellares is seeking an innovative and motivated Research Associate with expertise across cellular biology and engineering to join the R&D group within the Process Development team. This individual will interface across many parts of the company and contribute significantly to the development of our advanced cell therapy manufacturing platform. The primary focus of this position is to support the design and execution of collaborative experiments that span biological, engineering and technology development. This work will help establish and optimize the fundamental performance capabilities of Cellares' hardware, software and infrastructure, generating cross-cutting datasets and guidances that will benefit all programs. The ideal candidate will have a strong science and engineering background, with demonstrated experience with cell culture, cell purification/selection and/or genetic manipulation. Expertise within mechanical, chemical, software and/or systems engineering would further position a candidate to succeed in this role. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad range of challenges as the company grows.
\n Responsibilities Design and execute mammalian cell therapy process development and hardware testing experiments using scientific principles and statistical approaches (DOE) Interface cross-functionally with Systems and Software Engineering teams to test new technologies relevant to process onboarding and Cell Shuttle performance optimizationAnalyze and present technical results at departmental meetingsContribute to high-quality technical documents, procedures, reportsBecome quickly adept at identifying bottlenecks and opportunities through hands-on independent and collaborative investigationsGather and review system requirements, develop robust test plans, oversee and support execution of experimentsDevelop training materials for process protocols and techniques, and onboard new team members as neededServe as subject matter expert where appropriate for cell therapy process technology improvements, and represent Process Development as needed RequirementsBS/MS or equivalent in Bioengineering, Chemical Engineering, Biology, Biochemistry, or related field0-4 years of process development or cGMP manufacturing experience in the cell therapy or bioprocessing fieldStrong understanding of cell biology and engineering principlesExperience designing experiments and troubleshooting semi-automated instrumentsHands-on experience with cell culture, gene editing, magnetic selection, etc. preferredExcellent verbal and written communication skills; able to interpret, summarize, and present scientific results in a clear manner to technical and non-technical audiencesCreative, self-motivated, eager to take on a wide variety of tasks and grow with the evolving technologySelf-awareness, integrity, authenticity, enthusiasm and a growth mindset
\n$25 - $50 an hour
Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, and Onsite lunches. All displayed pay ranges are approximate, negotiable, and location dependent.
\nThis 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.