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Automation Specialist

Planet Pharma
South San Francisco, CA Posted Oct 9, 2026
On-site

About this role

Automation Specialist

Location

South San Francisco, CA

Category: Technology

Salary

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Country: United States

Employment: Contract

Worksite: On-Site

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Job Description

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.

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 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:

PhD with 0-3 years of experience or Masters 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.

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

Pay Rate Range: 45-55/hr depending on expereince

Equal Opportunity Employer

We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us(opens in new tab) directly so that we can explore the appropriate arrangements.

Fraud Alert

Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.

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