Associate Scientist, Process Development (I,II,III)

Associate Scientist, Process Development (I,II,III) Cellares South San Francisco, CA Job Details Full-time $90,000 - $210,000 a year 1 day ago Benefits Stock options Health insurance Dental insurance Vision insurance 401(k) matching Qualifications Advanced cell culture techniques Content creation for technical audiences Technical documentation Technical writing within manufacturing Manufacturing standard operating procedures Policy & process development Laboratory standard operating procedures Automated systems Technical troubleshooting support Laboratory information systems (LIS) Sterile laboratory techniques Standard operating procedures (SOPs) Standard operating procedures drafting Full Job Description Position Summary Cellares is seeking an innovative and highly motivated Associate Scientist to join 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 design and execute experiments, as well as develop standard operating procedures and processes for the Cellares platform. The ideal candidate will be well-versed in process development techniques and methodologies, technology transfer, method scale up and troubleshooting, as well as engineering principles and tools. The successful candidate should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. Responsibilities Provide hands-on support to small-scale and scale-up experiments and overall development of the Cellares advanced cell therapy manufacturing platform Interpret and adapt a cell therapy manufacturing process from a client to the Cellares platform; design and execute experiments related to workflow development and scale-up Develop process diagrams and flowcharts for novel and existing processes Create project plans, timelines, and reports to inform project execution; address blockers and challenges during execution Perform primary cell line maintenance and leukopak processing, including isolation, activation, gene modification, expansion and cryopreservation Draft and review work instructions, standard operating procedures, test plans, and reports Generate and review process documentation including but not limited to Manufacturing Batch Records and Bill of Materials (BOM) Analyze and interpret process data, prepare presentations and present technical results Identify and investigate process deviations and non-conformances, document findings and implement effective corrective and preventive actions Requirements BS or MS in Bioengineering, Chemical Engineering, Biology, Biochemistry, or related field with 4-10 years of process development experience in the cell and gene therapy field Experience in aseptic technique and primary immune cell culture Extensive experience using and troubleshooting semi-automated instruments and laboratory information management systems Strong problem-solving skills and attention to detail Strong technical writing skills and experience authoring SOPs and reports Familiarity with cell therapy analytical testing methods, such as flow cytometry and cell-based assays is preferred 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 $90,000 - $210,000 a year Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent. 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. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.