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

    - South San Francisco
    Job DescriptionJob DescriptionPosition SummaryCellares is seeking an i... Read More
    Job DescriptionJob 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

     

     

    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 and identifying potential inconsistencies or verification signals in application materials based on available information. 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.

    Read Less
  • Research Associate, Process Development (I,II,III)  

    - South San Francisco
    Job DescriptionJob DescriptionPosition SummaryCellares is seeking an i... Read More
    Job DescriptionJob DescriptionPosition Summary

    Cellares is seeking an innovative and highly motivated Research Associate 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 support the design and execution of experiments, as well as development of standard processes using the Cellares platform. The ideal candidate will be multidisciplinary and have hands-on experience in process development. 

    Candidates should also enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.

    Responsibilities

    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

    Requirements

    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

    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.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 and identifying potential inconsistencies or verification signals in application materials based on available information. 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.

    Read Less
  • Automation Equipment Engineer (I, II, III)  

    - South San Francisco
    Job DescriptionJob DescriptionPosition SummaryCELLARES, South San Fran... Read More
    Job DescriptionJob Description

    Position Summary

    CELLARES, South San Francisco FacilityFULL-TIME 3rd Shift

    We are seeking an Automation Equipment Engineer to provide hands-on technical ownership of the automation equipment and control systems that power our advanced cell therapy manufacturing platform. This team is dedicated to bridging the gap between operations and engineering.

    The primary focus of this position is to troubleshoot, assess, and sustain automation equipment, as well as identify opportunities for future improvements. You will serve as the first point of contact for issues and work collaboratively with Operators, Scientists, and Engineers to mitigate and resolve them.

    Candidates 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

    Ensure equipment readiness by monitoring fleet health, responding to production issues, and supporting proactive testing

    Troubleshoot equipment and control systems including, sensors, motors, pumps, pneumatic actuators, PLC logic, six-axis robots, and software interfaces

    Identify recurring patterns and improvement opportunities, and feed those findings back to the R&D team to inform permanent enhancements to the platform

    Develop and maintain runbooks, troubleshooting guides, and operational procedures

    Coach operators and technicians through real-time questions, helping the broader team build comfort with the control systems

    Support commissioning and validation activities for automation changes and new systems

     

    Requirements

    Bachelor’s in Electrical Engineering, Mechatronics Engineering, Systems Engineering, Process Engineering, or equivalent experience

    2+ years supporting automated production equipment, preferably within medical device or pharmaceutical manufacturing contexts

    Hands-on experience wiring, configuring, and verifying electrical and control systems

    Working knowledge of industrial communication protocols such as EtherCAT, Modbus TCP/IP, serial interfaces, and OPC-UA

    Comfortable reading P&IDs, electrical schematics, and other technical drawings

    Reading proficiency in IEC 61131-3 Structured Text and experience working with at least one major PLC platform (Beckhoff TwinCAT, Siemens TIA Portal, B&R)

    Experience supporting integrated articulated robots (Kuka, ABB, Staubli, Fanuc)

    Experience working in a GMP or comparably regulated environment, and comfort operating within change control, deviation, and CAPA processes

    Must be able and willing to work an off-shift schedule (nights and/or weekends), with occasional travel (<15%)

    Self-awareness, integrity, authenticity, and a growth mindset

    Preferred Skills/Experience

    Direct production experience with Beckhoff TwinCAT 3 and TwinSAFE

    Experience with at least one major HMI / SCADA platform (Ignition, Wonderware, WinCC)

    Familiarity with time-series and log tooling (e.g., InfluxDB, Grafana) for equipment diagnostics

    Familiarity with Git or other source control for navigating code repositories

    Proficiency in Python or another scripting language for ad-hoc data extraction and analysis

    Prior experience supporting cell therapy, biotech, semiconductor, or other high-mix, high-stakes automated manufacturing platforms

     

    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 and identifying potential inconsistencies or verification signals in application materials based on available information. 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.

    Read Less
  • Manufacturing Support Services Specialist  

    - Somerset County
    Manufacturing Support Services Specialist Night Shift: 6 PM- 6 AM We a... Read More
    Manufacturing Support Services Specialist Night Shift: 6 PM- 6 AM We are seeking an innovative and highly motivated Manufacturing Support Services Specialist to join our Operations team who will contribute to the manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day warehouse operations. This is a hands-on position that will train in the Manufacturing and Warehouse Team. Candidates 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 Perform routine procedures following written instructions (SOPs, batch records, solution documents, protocols, etc.) Execute basic manufacturing processes in a GMP environment, e.g., buffer or media preparation, usage of controlled rate freezers, and LN2 tanks Support sample management and transport using LIMS Support Warehouse team with receiving of inbound consumables, labeling, and put-away using SAP and label printers Operate a forklift to accomplish warehouse duties Supports the maintenance and supply of warehouse storage Perform routine clean room and laboratory activities, including ordering of consumables and PPE items, cleaning, restocking, and equipment qualification/maintenance Operate in a controlled GMP environment and perform gowning as per procedure Complete required training and ensure compliance with established internal and external control procedures Responsible for revising and originating production records and standard operating procedures Initiate and support the closure of Deviation Reports and CAPAs Train and mentor new manufacturing support services associates on procedures, aseptic techniques, equipment, and troubleshooting skills Review in-process and completed documents for accuracy and to make sure batch records are turned in to area management within the specified days of completion Provide user feedback to engineering and process teams, support with requirements gathering and review Work with Quality Control, Facilities, Materials Management, Quality Assurance, and Validation to complete assignments Other duties as assigned Requirements Bachelor's Degree or a diploma in a scientific or related field is preferred 1-2 years of experience within the biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy Must know and follow job safety procedures, attend required health and safety training, proactively promote safety at work, and promptly report actual and potential accidents and injuries. Must comply with the safety policies of the company and site Ability to lift 30 pounds Adherence to cGMPs is required at all times during the manufacturing of Cell Therapy products SAP and LIMS experience is preferred Proficiency in Drug Product-related process equipment Must have experience following protocols, SOPs, and/or GMP documentation Excellent verbal, written, presentation, and interpersonal skills Strong analytical and problem-solving skills Self-motivated and passionate about advancing the field of cell therapy Self-awareness, integrity, authenticity, and a growth mindset Desire to be part of a rapidly evolving organization, with compelling technology, and take products and processes to the next level $28 - $38 an hour 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. Read Less
  • Senior Electrical Engineer (I, II, III)  

    - South San Francisco
    Job DescriptionJob DescriptionPosition SummaryCellares is seeking a Se... Read More
    Job DescriptionJob Description

    Position Summary

    Cellares is seeking a Senior Electrical Engineer passionate about electrical design and automation who will contribute significantly to the development of our advanced cell therapy manufacturing platform. 

    The position will be focused on electrical systems within cell therapy manufacturing equipment, including design, documentation, and validation of control panels, PCBAs, and interconnecting cabling. You will interface across many parts of the company to develop novel products used in the cell and gene therapy world, and will have the opportunity to grow your career under the mentorship of a top-notch cross-functional engineering team. 

    Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle a broad array of challenges as the company grows

    Responsibilities

    Lead electrical design for complex automation equipment, ensuring compliance with relevant regulatory and safety standards such as IEC 61010, NFPA 70/79, and UL 508A

    Design power and signal distribution throughout industrial equipment using control panels, cables, PCBs, and off-the-shelf assemblies

    Document Electrical designs in schematic, interconnect, and layout drawings in a formal Product Lifecycle Management paradigm

    Assist with the development of functional requirements and specifications

    Design and implement test benches to support prototyping and characterization

    Participate in design reviews and provide input to identify issues and drive design choices

    Collaborate with controls, mechanical, systems, and software engineers

    Requirements

    Bachelor’s degree in Electrical Engineering and at least 7 years of experience, or a Master’s degree with at least 5 years of experience

    Experience working on projects incorporating electrical and mechanical components, and general exposure to different types of sensors and actuators

    Solid understanding of AC and DC power distribution, including circuit protection, sizing, and design for manufacturing

    Experience integrating PLC hardware platforms such as Beckhoff, Siemens, Allen-Bradley, etc.

    Familiar with digital communication mediums such as Ethernet, RS-232, RS-485, and how they work at a physical level

    Hands-on experience in digital and analog electronic circuit design, troubleshooting, and testing

    Proficient with standard electrical test equipment such as DMM, oscilloscope, function generator, etc

    Ability to build prototypes, construct electrical panels, perform wiring, and cable routing

    Self-awareness, integrity, authenticity, and a growth/entrepreneurial mindset

    Preferred Experience

    Proficiency with Electrical CAD software such as EPLAN, Zuken, AutoCAD Electrical, Solidworks Electrical, OrCAD, Altium, etc.

    Proficiency in designing PCB assemblies

    Experience with a programming language such as Python, Structured Text, Ladder Logic, C# or C

    Exposure to 3D CAD software such as SolidWorks, Inventor, Fusion 360

    Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, 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 and identifying potential inconsistencies or verification signals in application materials based on available information. 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.

    Read Less
  • Automation Engineer (I, II, III)  

    - Bridgewater
    Job DescriptionJob DescriptionWe are seeking an Automation Engineer to... Read More
    Job DescriptionJob DescriptionWe are seeking an Automation Engineer to support the development, validation, and day-to-day operation of fully automated QC testing workflows in a regulated GMP environment at our Bridgewater, NJ site. This role is central to the success of our Cell Q platform and commercial-scale QC operations.
    The successful candidate will play a key role in transferring, scaling, and optimizing automated QC test methods across multiple automated workcells, while also providing hands-on runtime operational support for the Cell Q platform and the broader QC laboratory infrastructure. This includes troubleshooting systems, supporting production testing, and ensuring consistent, compliant execution of automated workflows.
    Working closely with cross-functional partners in Quality Control, Analytical Development, Manufacturing, IT, and Quality, the Automation Engineer will contribute to system validation, user training, technical documentation, and controlled version management of automated test methods under change control. In addition, this role will help design, implement, and maintain automated sample and reagent management workflows that enable scalable, reliable, and robust end-to-end processes for high-throughput QC testing in a GMP setting.
    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.
    ResponsibilitiesSupport the transfer and validation of automated QC workflow stepsValidate and optimize automated methods for sample preparation, analysis, and data collectionMonitor system performance, track recurring issues, and collaborate with engineering and quality teams to implement technical and procedural improvementsConduct validation testing of liquid handling methods and integrated systems to ensure proper functionality and performanceAnalyze automation workflows to identify bottlenecks and areas for optimizationDevelop and implement troubleshooting methodologies to identify and resolve QC test method issuesProvide automation system and instrumentation support and troubleshootingRequirementsBachelor's or higher degree in Engineering, Computer Science, Biotechnology, or a related field2+ years of experience designing, implementing, and maintaining laboratory automation systems.Experience programming and optimizing liquid handling methodsExperience developing and implementing integrated automation solutions using Biosero’s Green Button Go softwareExperience with laboratory analytical instruments and automated systemsExperience integrating and managing assay results with LIMSFamiliar with flow cytometry, genomic, and cell-based assaysStrong technical writing skills and experience authoring Standard Operating Procedures (SOPs), documentation, and training materials Excellent problem-solving skills and the ability to troubleshoot technical issues.Strong communication skills to collaborate effectively with cross-functional teams.Attention to detail and the ability to work independently and manage multiple tasks simultaneously.Creative, self-motivated, eager to take on a wide variety of tasks and grow with the evolving technologySelf-awareness, integrity, authenticity, and a growth mindset
    Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, 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 and identifying potential inconsistencies or verification signals in application materials based on available information. 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.

    Read Less
  • Automation Engineer (I, II, III)  

    - South San Francisco
    Job DescriptionJob DescriptionWe are seeking an Automation Engineer to... Read More
    Job DescriptionJob DescriptionWe are seeking an Automation Engineer to contribute to the development, implementation, and optimization of innovative lab automation systems. The role involves enabling scalable and robust end-to-end automated workflows for high-throughput cell therapy manufacturing QC testing. 
    The successful candidate will play a key role in developing and managing liquid handling methods, as well as supporting the integration of specified off-the-shelf instruments and custom hardware within a fully automated workcell. Collaborating closely with cross-functional teams, the hire will contribute to iterating on various aspects of system designs and developing strategies for workflow optimization. Additionally, the role involves leading the development and testing of specific verification and validation plans for our automation systems.
    Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle a broad selection of challenges as the company grows.ResponsibilitiesTransfer and validated manual to automated QC workflow steps Develop, validate, and optimize automated methods for sample preparation, analysis, and data collectionDesign and execute validation experiments to optimize assay and workflow parametersConduct verification and validation testing of integrated systems to verify proper functionality and performanceAnalyze automation workflows to identify bottlenecks and areas for optimizationImplement troubleshooting methodologies to identify and resolve complex assay method issuesRequirementsBachelor's or higher degree in Engineering, Computer Science, Biotechnology, or a related field2-4+ years of experience designing, implementing, and maintaining laboratory automation systemsExperience programming and optimizing liquid handling methodsExperience developing and implementing integrated automation solutions using Biosero’s Green Button Go softwareExperience with laboratory analytical instruments and automated systemsExperience integrating and managing assay results with LIMSFamiliar with flow cytometry, genomic, and cell-based assaysStrong technical writing skills and experience authoring Standard Operating Procedures (SOPs), documentation, and training materials Proficiency in programming languages such as Python or C#Excellent problem-solving skills and the ability to troubleshoot technical issuesStrong communication skills to collaborate effectively with cross-functional teamsAttention to detail and the ability to work independently and manage multiple tasks simultaneouslyCreative, self-motivated, eager to take on a wide variety of tasks and grow with the evolving technologySelf-awareness, integrity, authenticity, and a growth mindsetCellares 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 and identifying potential inconsistencies or verification signals in application materials based on available information. 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.

    Read Less

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