Laboratory Automation Specialist

Date Posted: 10/08/2026 Hiring Organization: Rose International Position Number: 508903 Industry: Biotech/Healthcare Job Title: Laboratory Automation Specialist Job Location: South San Francisco, CA, USA, 94080 Work Model: Onsite Shift: 8 am - 5 pm (Mon - Fri) Employment Type: Temporary FT/PT: Full-Time Estimated Duration (In months): 13 Min Hourly Rate($): 54.00 Max Hourly Rate($): 58.00 Must Have Skills/Attributes: AI, C#, DATA MANAGEMENT, Python, SOP Experience Desired Experience in biomedical engineering, chemical engineering, mechanical engineering and biomaterials (4 yrs), Cell culture automation experience, particularly with 3D cell culture, organoids, spheroids, iPSC or complex in vitro model (4 yrs), Programming and systems integration experience using Python/C#, automation scheduling software, and/or LIMS/data integration. (4 yrs) Required Minimum Education: Master’s Degree Preferred Education: Ph.D / Doctorate **C2C is not available** Job Description Required Education: Masters Degree with 4-6 years of experience in biomedical engineering, chemical engineering, mechanical engineering, biomaterials, immunology, pharmacology, cellular or molecular biology, toxicology, pharmaceutical sciences, or a related field is required. Preferred Education PhD with 0-3 years of experience Overview A member of the Client Group, Client has been at the forefront of the biotechnology industry for more than 4-5 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Client has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Client where we believe that our employees are our most important asset & are dedicated to remaining a great place to work. The Position We are looking for a versatile Automation Specialist to work within the Complex in vitro Systems (CiS) Laboratory, where we design, develop, and characterize complex in vitro models (CIVM) to support the larger Development Sciences, Research, and Translational Medicine departments of Client. In particular, the individual will be working in a cross functional team dedicated to providing technical expertise to automate scaling, processing, and assays using CIVMs. Currently the CIVMs include 3D multicellular models consisting of organoids and spheroids with aspiration to automate microfluidic organ-on-chip technologies. Our CIVM assays are developed to support both discovery and preclinical development portfolios broadly through multiple contexts of use, including safety, disposition, biomarker development, and pharmacodynamic responses. As part of the CiS Technologies team that establishes, qualifies, executes and maintains innovative, state-of-the-art technologies/platforms, we are looking for someone who will help us drive process and data integration and focus on advancing the operational capabilities of our automation and liquid handling systems. In This Laboratory-based Role Your Impact Will Include Work in a dynamic and innovative team to pioneer automation of CIVM culture (e.g. organoids, iPSC models, etc.) and assays. Collaborate with scientists to translate manual cell culture and assay experiment processes into new automated workflows, including programming, testing, qualification and execution. Qualify and execute automated CIVM culture and assays on our integrated liquid handling system Perform regular maintenance tasks and dry tests to ensure the readiness and sterility of the automation platforms Drive the integration of data management, analysis pipelines and data automation by aligning with internal and external stakeholders. Train and support team members in formalizing Python development practices, including version control, collaborative workflows, and AI tool integration, with a focus on biology applications. Document and report all relevant processes using SOPs, and share capabilities with colleagues in and outside the group in presentations, open door sessions and lab tours. This position is laboratory-based and will include: sitting or standing for extended periods, performing repetitive tasks such as cell culture, pipetting and labeling tubes, performing techniques involving a high degree of manual dexterity and physical activity, flexibility as to work schedule (i.e. may need variation in hours worked and timing of those hours which may include weekend/holiday work as needed only), work with potentially hazardous materials including, but not limited to chemotherapeutics, biological hazards, and human primary cells. Who You Are The ideal candidate will design, develop, operate, and maintain automated protocols and systems for complex cell culture and assay process scale up. The successful candidate will work closely with other automation specialists and biologists at Client to ensure regular maintenance of instrumentation and perform quality control of automated systems and equipment. They will also collaborate with a team of external vendors, data engineers, and software developers to implement automation best practices and proper process metadata tracking with Laboratory Information Management Systems (LIMS) integration. Importantly, the candidate will have direct experience translating lab experiments developed by individual scientists into automation-ready protocols that can run repeatedly at scale. Successful Candidates Will Possess The Following Skills/attributes Candidates must have experience in automation of cell culture in either academia, pharmaceutical/biotechnology industries, or contract research organizations. Experience with automation and/or implementation of CIVMs is a plus. Experience operating, programming, and integrating automation instrumentation and peripherals including but not limited to liquid handling platforms (e.g. Hamilton, Biomek, Opentron, BioTek washers), automated incubators, centrifuges, analyzers, and imagers. Experience working with Python and/or C# and enjoy solving challenges systematically by using your analytical and technical skills Experience with automation scheduling software (e.g. GreenButtonGo, Thermo Momentum, HiRes Cellario, etc.) is highly preferred Experience with integrating instrument and process quality control (QC) data with LIMS tools Track record of translating hands-on cell culture work into automated protocols Hands on experience with at least several cellular assays (cell viability, flow cytometry, gene expression analysis, high content screening, 3D imaging analysis, biomarker quantification, transepithelial electrical resistance (TEER), etc.) is of advantage Hands on experience with primary cell cultures in 3D is a plus (could be organoids, layered cultures, or spheroid work) Experience troubleshooting automation systems & workflows and ability to prioritize in a multi-user and multi-application environment. Coordinating with external vendors and service providers for hardware/software modifications, driver requests, and system maintenance. Maintain comprehensive technical documentation for automation systems, procedures, and troubleshooting guides to ensure knowledge transfer and system maintainability. Passionate about collaborating in a cross-functional team in a multicultural environment. Strong communication skills and ability to efficiently interact with scientists with different backgrounds and limited experience with automation. Strong organizational skills, attention to detail, ability to prioritize tasks, interact professionally and present data to all levels of staff and external partners is required**Only those lawfully authorized to work in the designated country associated with the position will be considered.****Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.** Benefits For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website. California Pay Equity For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here. Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances. If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department. Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).