Rezo Therapeutics is a biopharma company that aims to increase the success rate of drug development by building a disease-agnostic, fully-integrated, network biology platform.

We are leveraging a unique integrated approach, combining capabilities in genetics, proteomics, structural biology and AI to generate deep biological insights and novel therapeutic approaches.

Located in San Francisco's vibrant Mission Bay neighborhood, Rezo is in close proximity to UCSF, numerous urban amenities, and outdoor recreational opportunities.

Responsibilities

If you do not see a job listing that matches your specific background, please apply to this posting as we will be looking for exceptional individuals in the following areas:

Proteomics

• Develop industry scale assays using in-house mass spectrometers
• Execute platform projects centered on PPI mapping, proximity labeling, post-translational modification and abundance proteomics
• Support drug discovery campaigns and develop target-based screens

Genetics

• Develop multimodal single and combinatorial genetic screens using CRISPR technologies
• Collaborate with target discovery teams to provide genetic support for targets and drug MOA

Chemical Biology and Protein Sciences

• Develop HTS small molecule screening campaigns and create robust target assays for drug development
• Drive enzymology, biophysics and protein binding analysis efforts
• Help build out the structural biology platform (including crystallography & Cryo-EM)
• Develop chemical biology tools to map ligandable pockets and aid in drug development

Cancer Biology

• Implement cutting edge molecular and cellular techniques to determine target functions in cell-based solid tumor models
• Develop data packages to prioritize targets and nominate candidates to the drug discovery stage
• Individuals with expertise in oncogene/tumor suppressor pathways and/or drug resistance are especially encouraged to apply

Computational Biology, Data Science

• Develop novel algorithms and apply deep learning-based approaches to network and proteomics datasets
• Implement cloud infrastructure, pipelines, and UI/UX for data analytics
• Conduct bioinformatic and statistical analyses of large, multimodal datasets

Benefits

• Medical (HMO or PPO), dental, and vision insurance
• Discretionary time off policy
• Company holidays (including summer and winter shutdown)
• 401(k) retirement savings program
• Commuter / Mass Transit Benefit Program
• Healthcare Flexible Spending Account (FSA)
• Dependent care Flexible Spending Account (FSA)
• Parental leave
• Competitive compensation
• Flexible work schedule

Equal Employment Opportunity

At Rezo we value a diverse, equitable, inclusive workplace and provide equal employment opportunity to all persons without regard to race, color, sex, gender identity, gender expression, religion, age, national origin, ancestry, citizenship, physical or mental disability, medical condition, family care status, marital status, domestic partner status, sexual orientation, genetic information, military or veteran status, or any other basis protected by federal, state or local laws.

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The role reports to Manager, Scientific Operations. This role will be an onsite role based in our Brisbane, California headquarters.

Responsibilities:

• Perform routine lab work including pre-analytical sample processing, plasma isolation, and downstream genomics and proteomics assay processing.
• Operate liquid handler instruments to carry out experiments.
• Troubleshoot instrument and sample processing errors as needed; escalate and report issues through appropriate channels as needed.
• Identify and implement process improvements across the lab by thinking critically about the execution of all experiments.
• Verify all aspects of incoming specimens and assess acceptability for analytical testing.
• Maintain documentation for executed experiments.
• Perform equipment maintenance according to the laboratory's standard operating procedures for the following but not limited to: Hamiltons, Biosafety Cabinets, centrifuges, freezers, refrigerators, and pipettes, as needed.
• Assist with training of new laboratory personnel and training of new procedures with existing personnel.
• Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications.
• Report all concerns of test quality and/or safety to the Supervisor or Safety Officer.
• Perform other miscellaneous laboratory duties as assigned and assist others as time allows.

Requirements:

• Bachelor's degree or Master's degree in molecular biology, biochemistry, genetics, chemical biology, or a related field.
• 2+ years relevant industry experience in a laboratory setting.
• Experience working with 96 or 384 well plate format assays.
• Proven track record of following SOPs, work instructions or experimental designs to completion.
• Strong organizational skills and attention to detail.
• Ability to work, execute, and troubleshoot protocols independently.

Nice to Have:

• Working understanding of GLP.
• Experience with NGS library preparation and/or sequencing.
• Experience with ELISA, Luminex, or other immunoassays.
• Familiarity with Liquid Handlers - Bravo, Hamilton, etc.

Benefits and Additional Information:

The US target range of our hourly rate for new hires is $37.68 - $46.69. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education.

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You will create, plan and execute software development plans while ensuring efficiency, scalability and usability for our Commercial, Laboratory, and R&D teams. You will gather requirements and prioritize technical development in alignment with cross-functional teams and stakeholders.

This role will lead discussions with key-decision makers and stakeholders to create a comprehensive data platform roadmap outlining Freenome's path to commercialization and support for ongoing product development. You will work closely with our engineering team, leveraging your deep knowledge in Agile methodologies (Scrum, Kanban, sprint planning, etc) to enable seamless execution.

The role reports to the Associate Director, Technical Product Management. This role will be a Remote role, with onsite travel to our headquarters in Brisbane, California as needed.

As a Technical Product Manager, you will:

• Define requirements and manage the development processes, systems, and software infrastructure for the data platform and tools supporting Commercial and R&D initiatives.
• Partner with lab and business stakeholders to elucidate requirements, optimize workflows, and lead data platform and product definition, ensuring alignment with regulatory standards (e.g., HIPAA, HITECH).
• Work with engineers to translate product requirements into Epics and Stories with clear user acceptance criteria.
• Track and drive development and ensure fulfillment of requirements using issue tracking system (e.g., Jira).
• Lead and facilitate productive interactions between users and engineers to ensure user needs are understood and met.

You will create a thorough technical strategy and roadmap to scale Freenome's commercial data platform, tooling, and data products to support current and future products. Provide a clear and tangible vision for future development efforts with scalability and accessibility in mind.

Ensure complete data integrity throughout the pipeline with technical and process-oriented solutions.

Must have:

• Bachelor's degree in an analytical, technical, or scientific field; advanced degree preferred.
• At least 5 years of experience in a software development environment, ideally within biotechnology and NGS.
• Deep expertise in identification and prioritization of software features.
• Demonstrated ability to successfully lead complex trade-off decisions between functions and measurably improve organizational success and processes.
• Experience leading software development efforts to meet regulated market standards (FDA, CAP/CLIA), laboratory operations, medical affairs, or clinical study operations for diagnostics.

Nice to have:

• Experience in building solutions with a focus on multiomics, NGS, or proteomics a plus.

Benefits and additional information:

The US target range of our base salary for new hires is $118,150 - $167,475. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education.

We invite you to check out our career page @ https://freenome.com/job-openings/ for additional company information.

Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Applicants have rights under Federal Employment Laws.

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