{"domain": "directsourcepro-rch.com", "user": "", "isWillingToRelocate": false, "isUserAuthenticated": false, "isUserETXCandidate": false, "isDomainETX": false, "isDomainVeteran": false, "signUpConfig": {}, "getHelpButton": {}, "isCareerPlannerEnabled": false, "enableRememberMeOption": false, "isMyApplicationsEnabled": false, "showVeteranEmployerSignUp": false, "enableUserPreferenceSelection": false, "isUserPreferenceApplied": false, "candidate": {"enc_id": 0, "fullname": "", "firstname": "", "lastname": "", "email": "", "phone": "", "location": "", "filename": null, "starred_positions": [], "resumeUrl": "", "onboardingCompleted": false, "isUserInPcsIjp": false}, "branding": {"page_title": "Contractor Positions for Roche and Genentech", "enableTalentNetwork": 1, "showJobId": 1, "hideSearchPanelHeader": true, "homePageHeroBanner": {"title": "Contractor Positions for Roche and Genentech Powered by PRO Unlimited", "image": "https://static.vscdn.net/images/careers/demo/directsourcepro-rch/New+Roche+image", "color": "#000000"}, "privacyLink": "https://eightfold.ai/privacy-policy/", "privacy": {"text": "<div class='main-container'><p>Please confirm that you agree to the <a href= https://cloud.kapostcontent.net/pub/15c2e367-3926-47cd-b537-c22ed1191720/directsource-pro-privacy-policy?kui=IWeABt_VHYAgW78OUaTwIQ target='blank'>Data Privacy Policy.</a></p></div>", "button": "Confirm", "title": "Data Privacy Policy"}, "companyName": "Roche", "navBar": {"color": "#FFFFFF", "image": "https://static.vscdn.net/images/careers/demo/directsourcepro-rch/New+Roche+generic+logo", "link": "https://directsourcepro-rch.prounlimited.com/careers", "background": "#FFFFFF", "title": "Roche"}, "custom_style": {"font": "https://fonts.googleapis.com/css?family=Open%20Sans", "css": ".nav-item a { color: #fff !important;} .refer .user-name { color: #fff !important; } \n.upload-resume-modal {overflow: scroll !important;\n} \n.hero-image {height: 400px !important;} .upload-resume-modal .privacy-agreement p {text-align: left !important; display: -webkit-box !important;\n\n list-style-position: inherit !important;\n text-indent: initial !important;\n ul {list-style-type: none; !important;} li {\n position: relative !important;\n left: -10px !important; display:block !important; margin: 0 !important; padding: 0 !important; margin-bottom: 5px !important; }} .upload-resume-modal .privacy-agreement {\n width: -webkit-fill-available !important;\n float: left !important;\n margin: 0 !important;\n display: inline-block !important;\n font-family: 'Helvetica', 'Arial', sans-serif !important;\n font-size: 11pt !important;\n line-height: 20px !important;\n margin-bottom: 20px !important;\n}.join-tn-link {color: #333333 !important;}.jumbotron h1 {color: #000000 !important;} .jumbotron h1 {text-align: center !important; color: #000000 !important} .jumbotron h1 {margin-top: 100px !important}.jumbotron h1{padding-left: 25px !important;}, .position-title line-clamp line-clamp-2 {color: #0066CC !important;}, .position-apply-button{background: #0066CC !important;} .fixed-top{text-align:right !important; padding-right: 20px !important} .navbar img{padding-right: 30px !important} .navbar {position:fixed; z-index: 99999; }"}, "custom_html": {"page-footer": "<p className='body-text-2'><a title='Visit Eightfold.ai homepage' target='_blank' rel='noopener noreferrer' style={{ color: 'black' }}><img src='https://static.vscdn.net/images/pro_direct_source.svg' alt='' width='100' height='11' align='middle' style='margin-bottom: 3px'/> &thinsp; %(text)s PRO Unlimited & eightfold.ai</a> </p>", "page-footer-text": "powered By"}, "hideJobCart": false, "recaptcha_enabled": 0}, "positions": [{"id": 137451307082, "name": "Clinical Trial Leader III", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 1, "department": null, "business_unit": "Unknown", "t_update": 1656632532, "t_create": 1656632398, "ats_job_id": 137451307082, "display_job_id": 137451307082, "type": "ATS", "job_description": "Description: The Genentech Research and Early Development (gRED) Global contract Clinical Trial Leader (cCTL) is accountable for the strategic planning and execution of assigned early development global clinical trials [includes First-in-Human, Phase Ib, and other signal-seeking Phase I trials, and evidence of activity, proof-of-concept, dose-ranging, dual New Molecular Entity (NME), and other types of Phase II trials] under the direction of the Sr. Global Clinical Trial Leader (Sr. CTL). The cCTL is a member of one or more cross-functional Protocol Execution Teams (PETs). These complex programs focus on the rapid development of NMEs with limited clinical data, and as such, require implementation of novel and highly flexible global operational strategies to support exploratory hypotheses, including biomarkers and diagnostics. The cCTL enables the efficient delivery of global clinical studies, under the leadership of the Sr. CTL.", "stars": 0.0, "medallionProgram": null}, {"id": 137452503660, "name": "Bioinformatics Engineer", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1664298318, "t_create": 1664298080, "ats_job_id": 137452503660, "display_job_id": 137452503660, "type": "ATS", "job_description": "Description: Development Sciences Informatics seeks a talented and highly motivated Bioinformatics Software Engineer with expert knowledge of modern genomic data processing workflows and their application to cutting-edge biological sciences. The team you are joining supports gRED scientists with highly scalable and reproducible workflows for the analysis of pre-clinical and clinical sequencing data from transcriptomic, genomic, and (epi)-genetic assays at the bulk and single cell level. The primary focus of this position is to maintain and extend an orchestration system for high throughput genomic workflows to scale with the ever growing data volume and diversity as biology becomes a quantitative science. Your work will enable us to readily deploy our containerized workflows, with an emphasis on reproducibility and scalability, to public and private cloud environments so we can compute where the data resides. You are well informed about evolving and established data standards, workflow frameworks and relevant open source tools. You can evaluate and incorporate these tools into our data platform and complement them with your own software as needed. A successful candidate will collaborate with interdisciplinary teams of Software Engineers, DevOps engineers and Computational Biology Scientists to deploy and execute genomic workflows on thousands of samples and hundreds of projects at any given time. You are adapting our platform to new compute environments and continually make it more performant and robust. You are guiding our workflow developers to optimize their workflows for throughput, reliability and cost. Successful candidates will meet many of the following requirements Skills: You have expert knowledge of a modern genomic framework system (ideally cromwell/WDL, alternatively CWL, nextflow, toil) and have not only written workflows but have looked behind the curtain and deployed or configured the framework in a cloud environment You have expert knowledge of containerization in the context of genomic workflows, including automatic builds, CI/CD and container registries (e.g. dockstore, quai.io) You have successfully planned and implemented multiple software projects throughout the whole development cycle (planning, implementation, testing, release, maintenance) following modern software development practices. You are able to break down large problems into smaller software components and can develop them independently or as part of a large team. You have strong experience in the use of a high-level, object oriented programming language such as Python, Java and a strong understanding of Linux/Unix. You have knowledge of best practices for software engineering including but not limited to IaC, CI/CD, and software containerization. You are comfortable working both independently and collaboratively, and with handling several concurrent, fast paced projects. You are able to execute technical projects at global scale, across multiple teams and time zones. Strategic, analytical mindset and ability to innovate using technology to advance business goals. You have strong communication skills and can untangle and discuss complex technical tasks. Prior experience in a life science or drug development environment is beneficial.", "stars": 0.0, "medallionProgram": null}, {"id": 137452502061, "name": "Document Archiving Administrative Assistant", "location": "Oceanside, CA", "locations": ["Oceanside, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1664257122, "t_create": 1664256804, "ats_job_id": 137452502061, "display_job_id": 137452502061, "type": "ATS", "job_description": "Description: Document Archiving Admin provides Document Control and prepares equipment history records for off-site storage, in facilities, and engineering environments. Typical duties will include, but not be limited to: Maintain documents in a cGMP environment. Prepare archive records for off-site storage. Establish and maintain familiarity with the facility, its systems, and documentation. Verify documentation compliance with company and regulatory standards. Catalog, organize, file, and retrieve paper and electronic documents. Track the status of archiving document deliverables. Scanning of documents and publishing in Adobe Acrobat PDF. Upload converted electronic documents into CMMS (SAP) Database or other identified electronic document management repositories as required. Communicate status and issues to management. Fulfill site training requirements. Performance qualifications: Relevant degree or equivalent experience. Professional, positive attitude, and a passion for excellence. Proficiency in MS Office - Excel, Word. Adobe Acrobat publishing is a plus. Experience with file organization systems. High productivity without sacrificing accuracy. Self-directed and able to work with minimal supervision. Outstanding organization skills. Good office etiquette. Detail-oriented and thorough. Familiar with printers, copiers, and scanners. Ability to lift storage boxes in preparation for shipment (approx. 20lbs).", "stars": 0.0, "medallionProgram": null}, {"id": 137452502059, "name": "Administrative Assistant II", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1664256317, "t_create": 1664256245, "ats_job_id": 137452502059, "display_job_id": 137452502059, "type": "ATS", "job_description": "Description: Provides analytical and specialized administrative support to relieve and assist executive, administrative, line and staff managers of complex details and advanced administrative duties. May handle special projects and execute research and data analysis tasks. Analyses problems, determines approach, compiles and analyses data and prepares reports and recommendations. Coordinates activities between departments and outside parties. Contacts company employees at all organizational levels to gather information and prepare reports. Work is generally of a critical or confidential nature. Represents the department in a polished and professional manner Assignments may be in various functional areas. Responsibilities Supports assigned manager and team with a variety of routine administrative and operational activities including but not limited to: Coordinating, scheduling and preparing for meetings, events, domestic and international travel and conference calls, channeling communication and/or materials; Coordinating interview scheduling, office moves, office supply management and vendor communications; Creating and submitting purchase orders and compiling expense reports. Serves as the first point of contact, greets and assists visitors; screens incoming calls and takes messages. Provides general support on editing and formatting departmental documents such as memos, reports, presentations and legal documentation that may require some data gathering and analysis. Serves as the departmental information resource for general operational or administrative inquiries, requiring basic administrative knowledge of departmental and organizational policies and procedures. Supports the department with new systems, processes and training compliance. Supports the training and on-boarding efforts for new staff on administrative processes, systems, practices, tools, etc. Actively participates in internal company meetings with other administrative professionals, finds ways to apply new methods of working, improvements in work processes and supports an exchange of ideas among colleagues. Provides back-up support to other teams as necessary, demonstrating flexibility, adaptability and positive demeanor in the face of change. Participates in administrative project initiatives within or outside department/functional area. Education Details H.S. Diploma Associate's Degree Years of Experience 2 Experience Details 2 years Directly related administrative support experience. Experience supporting a department/functional team in the life sciences/biotechnology industry is strongly preferred.", "stars": 0.0, "medallionProgram": null}, {"id": 137452502057, "name": "Research Associate V", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1664256095, "t_create": 1664255732, "ats_job_id": 137452502057, "display_job_id": 137452502057, "type": "ATS", "job_description": "Description: Research Associate Job Description for the Cleaning, Compendial, and Materials Group Job Description: This position provides analytical support for cleaning verification activities and the testing of materials in support of R&D activities and GMP manufacture of Drug Substance and Drug Product. Analytical Techniques HPLC HPLC-MS FTIR KF Conductivity ICP GC UV pH Wet Chemistry (USP) Analytical Duties Developing and qualifying (validating) analytical methods capable of detecting low levels of residues on manufacturing equipment. Perform swab/rinse sampling on manufacturing equipment in accordance to the qualified method. Perform analysis on cleaning verification samples to determine drug and detergent residues. Communicate analysis results to his/her supervisor and to the appropriate teams. Support analysis of raw materials, excipients, packaging components, starting materials, and packaged clinical supplies using various analytical techniques. Residual Solvents testing by GC. Routine Water Analysis by KF. Compile new specifications for raw materials, excipients, and packaging components. Assist in the testing of drug substance and drug products as needed. Requirements BS/BA in a relevant scientific discipline. Candidates must have familiarization of analytical instruments, making buffers, hands on experience with pH meter, chromatography (HPLC and GC), and FTIR. Candidates should be detail-oriented and have good problem solving, written and oral communication skills. Full vaccination against COVID-19, defined as two weeks after final dose, is required for all contractors working onsite at Genentech facilities or leased facilities, unless otherwise exempt due to medical or religious accommodation. This is an ONSITE position.", "stars": 0.0, "medallionProgram": null}, {"id": 137452488902, "name": "Research Associate III", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663996612, "t_create": 1663996474, "ats_job_id": 137452488902, "display_job_id": 137452488902, "type": "ATS", "job_description": "Description: We are seeking an outstanding candidate to join the Biomolecular Resources Department. In this role, you will have the opportunity to be part of our state-of-the-art high-throughput subcloning pipeline to generate DNA constructs for recombinant protein expression and cell engineering in support of basic research, Small and Large Molecule Drug Discovery. The successful candidate will be responsible for generating DNA constructs in a timely manner through a combination of outsourcing and wetlab work, contributing to the advancements of the high-throughput subcloning platform in a core facility setting using automated liquid handling systems and bioinformatics tools. The ideal candidate will have deep expertise in standard and sophisticated Molecular Biology techniques and be able to partner with a variery of stakeholders throughout the organization. They will also thrive on standardizing and simplifying methods to construct complex DNA constructs. The successful candidate will be a team player with passion for quality work and timely delivery and enjoy working in a fast-pace, innovative environment. Requirements: Bachelors, or higher, degree in Biology/Biochemistry or a related scientific discipline with a minimum of 3 years experience, ideally in an industry or core facility setting. Extensive hands-on experience with Molecular Biology techniques in high-throughput formats. Detail oriented and comfortable in dealing with large data sets and distilling data to important points. Familiarity with molecular biology software, such as Benchling, Geneious Prime. Excellent agility to adapt to the changing needs and priorities for an organization to fulfill the business needs. A team-oriented individual who recognizes the strengths of everyone on the team and appreciates diverse viewpoints. Excellent communication, organization, time management and record keeping skills with a strong emphasis on data entry into the database. Experience with liquid handling equipment is a plus. Experience with protein expression is strongly desired.", "stars": 0.0, "medallionProgram": null}, {"id": 137452488888, "name": "Research Associate I", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663995647, "t_create": 1663995551, "ats_job_id": 137452488888, "display_job_id": 137452488888, "type": "ATS", "job_description": "Duties Responsibilities for this position would focus on animal studies including monitoring, dosing, and animal necropsy and organ collection. The individual will be expected to work with infectious and/or bio-hazardous reagents and material. The individual is also going to be involved with general lab managerial duties such as stocking and ordering supplies, maintaining lab cleanliness, autoclaving supplies, and appropriately disposing of biohazardous and chemical waste. Limited administrative functions such as attending select meetings, equipment and supply inventory, preparation of work schedules, etc are expected. Experience in handling animals with excellent in vivo dosing techniques, such as i.v., i.p., s.c., i.n., p.o., and animal organ collection and dissection techniques. Excellent skills in communication, organization, flexibility and an eagerness to learn. Must work well with others and be a team player. Must be capable of standing, lifting, kneeling, bending, etc., for extended periods of time, and must be willing to work with potentially hazardous materials, adhering to health and safety guidelines. BA/BS/MS or equivalent experience", "stars": 0.0, "medallionProgram": null}, {"id": 137452488887, "name": "Mechanical Engineer II", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663995350, "t_create": 1663995263, "ats_job_id": 137452488887, "display_job_id": 137452488887, "type": "ATS", "job_description": "Description: Key Requirements : 1\\. Computer aided design experience preferably Solidworks 2\\. Sound hands on experience of creating drawings and a thorough understanding of Geometric dimensioning and tolerancing (GD&T) 3\\. Experience of change management using product life cycle tools in preferably medical devices or any other highly regulated industry 4\\. Excellent analytical skills in regards to design calculations such as tolerance stackups, torque calculations etc 5\\. Hands on experience with risk assessment and excellent problem solving skills such as DFMEA, root cause identification, pugh analysis etc Summary Designs and analyses mechanical systems, equipment and packaging. Conducts feasibility studies and testing on new and modified designs. Directs support employees in the preparation of detailed design, design testing and prototype fabrication. Provides design information to drafting for packaging documentation. Responsibilities Practices and mentors in the use of company concepts, policies and procedures, familiar with and follows standard practices. Applies functional expertise routinely on the job. Receives general direction and exercises considerable discretion as to work details, and contributes to the definition and timely achievement of overall project goals. Participates or leads in efforts to define new components, products or processes; Identifies and solves technical challenges, implements improvements to work processes. Creates potentially patentable components for systems, or processes. Designs, plans and executes project related tasks. Designs and executes experiments to test hypothesis related to project outcomes, and applies advanced scientific knowledge to projects; determines priorities for experiments. Independently designs and executes experiments. Utilizes DOE as appropriate. Assures experimental quality through sound, independent, experimental design. Participates or leads cross-functional technical teams. Establishes interfaces across other organizational groups. Provides technical direction and feedback to others, teaches others and troubleshoots problems. Participates in project planning, process updates and contributes to experimental design. Prepares and delivers presentations of project results to others; presents data to larger and more diverse audiences. Monitors work to ensure quality, and continuously promote Quality First Time. Qualifications Bachelor's Degree or equivalent in a directly related discipline plus 8 years Minimum of related experience OR MS degree in directly related discipline + 4 years of related experience required OR PhD degree in directly related discipline + 2 years of related experience required. Demonstrates success in technical proficiency, creativity, collaboration with others and independent thought. Expert knowledge of engineering principles and concepts.", "stars": 0.0, "medallionProgram": null}, {"id": 137452488885, "name": "Data Scientist III", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663995154, "t_create": 1663995013, "ats_job_id": 137452488885, "display_job_id": 137452488885, "type": "ATS", "job_description": "Description: The Real Estate & Workplace Effectiveness (RE & WE), Workplace Digital Insights - Analytics (WDI-A) Data Scientist will report to the Director of Workplace Digital Insights - Analytics. This role presents a unique opportunity to apply data science to help Genentech build the workplace of the future and help understand how well groups are doing in their work environments. Analyses will inform the design of the Physical Work Environment, Social Agreements and Technology (e.g. advanced sensor technologies / IoT) so Genentech employees can be at their best when serving patients. Job Duties/Responsibilities: \u25cf Leverage data to discover patterns and solve strategic analytic business problems \u25cf Execute sophisticated analyses that result in actionable recommendations \u25cf Collaborate with subject matter experts across RE & WE and the business \u25cf Contribute to data integrity and data forensics efforts \u25cf Define requirements and work with local and global Informatics (IT) to extend and maintain the Site Services Analytics platform \u25cf Design and implement self-service reporting tools (e.g. R-Shiny, Tableau) \u25cf Identify opportunities to further build out our IoT strategy \u25cf Work independent as well as collaborating with other team members Competencies Identified for Success: \u25cf Achieving Results \u25cf Communication \u25cf Innovation \u25cf Teamwork & Collaboration \u25cf Technical & Business Expertise Qualifications: Education, Experience, Knowledge and Skills: (Minimum requirements) Minimum Qualifications \u25cf Degree in Data Science, Computer Science, Engineering, Psychology, Statistics, or related technical field or equivalent experience \u25cf Business Experience 5+ years of experience in data related fields - experience with research programs that seek practical/predictive (rather than only statistical) significance is particularly valued \u25cf Experience working with large, complex data systems to aggregate, organize, and prepare data for use in business analysis \u25cf Extensive background in data mining and statistical analysis to drive insights from data \u25cf Demonstrated experience in bridging business requirements and technical development \u25cf Strong background in statistical programming (preferably R, with Python as a plus) and data-oriented scripting (e.g. SQL) and \u25cf Classical statistics Preferred Qualifications \u25cf Advanced degree in Data Science, Computer Science, Statistics, or related technical field \u25cf Experimental design and analysis, including validating questionnaires, and designing surveys \u25cf Developing shared code (e.g., version control, programming patterns, libraries/packages) and creating data pipelines \u25cf Experience building R-Shiny applications \u25cf Experience working with Tableau \u25cf Machine learning approaches to fitting models (e.g., ensembles, bootstrapping) and estimating their performance (e.g., cross-validation) Desirable (not required) \u25cf Experience using web services, such as AWS, and big data toolkits \u25cf Architecture background/experience working with architects, space planners and interior design specialists \u25cf Experience working with HR / organizational people data \u25cf Publicly available examples of code (github, etc) or projects (websites, decks, publications)", "stars": 0.0, "medallionProgram": null}, {"id": 137452488884, "name": "Scientist II", "location": "Pleasanton, CA", "locations": ["Pleasanton, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663994721, "t_create": 1663994614, "ats_job_id": 137452488884, "display_job_id": 137452488884, "type": "ATS", "job_description": "Description: The Scientist II will be a member of the Research and Early Development Team in Pleasanton to support clinical sample processing which include nucleic acid extraction, library preparation, and Next Generation Sequencing. We are looking for an experienced candidate who understands both the technical and professional components of lab work. KEY ROLES & RESPONSIBILITIES Routinely execute standard molecular biology techniques, from DNA extraction to target enrichment and next generation sequencing library preparation Follow protocols precisely, and with extreme care under design control regulations and GMP laboratory conditions Be comfortable with and able to adapt to regular protocol changes as protocols are being developed and improved Regularly work with human biological samples including blood, plasma, tissue for nucleic acid extraction Routinely process multiple samples with accuracy and consistency Work under manager supervision to plan and conduct hands-on development and optimization experiments as needed Assume responsibility for timely completion of projects Be comfortable with changing priorities Accurately and consistently record sample tracking information, experimental methods, materials and results in electronic laboratory notebooks. Occasionally present findings and/or comprehensive project status reviews at internal seminars and department meetings. Apply technical writing skills to produce reports and documents. Skills: Ability to work under pressure with highly precious samples Strong laboratory proficiency and experience with processing multiple samples in a high through-put environment is highly preferred Familiarity with Microsoft Office suite of programs, especially Word, Excel, Powerpoint is preferred Experience with NGS based workflows including target enrichment, and library preparation is preferred Experience with sequencing on NGS platforms is preferred. Accurate record keeping a must Flexibility in working hours, especially during the training period a must Multichannel pipetting proficiency a must. 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