{"enableMapClustering": false, "isMyApplicationsEnabled": false, "domain": "directsourcepro-rch.com", "isThinProfile": 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"}, "recaptcha_enabled": 0}, "chatbot": false, "isHomePageLoad": true, "isWillingToRelocate": false, "locationInsights": null, "pcsTextConfiguration": {}, "showWizard": 1, "showVeteranEmployerSignUp": false, "mocTitle": null, "isSubQuery": false, "query": {"pid": "", "location": "", "seniority": [], "department": [], "query": "", "skill": []}, "showBusinessUnitInPositionSidebar": false, "location_used": "", "candidate": {"firstname": "", "lastname": "", "phone": "", "enc_id": 0, "onboardingCompleted": false, "isUserInPcsIjp": false, "filename": null, "location": "", "starred_positions": [], "fullname": "", "email": "", "resumeUrl": ""}, "installed_app_data": [], "candidateBuildProfile": {}, "location_user": "any", "isDomainVeteran": false, "facetNoTitlecase": null, "isUserAuthenticated": false, "candidateLogin": {}, "enhancementsEnabled": false, "isDomainETX": false, "veteranProgramDetails": [], "user": "", "getHelpButton": {}, "signUpConfig": {}, "isUserETXCandidate": false, "count": 107, "iframeImplementation": null, "recommended_star_threshold": 4, "userTitles": [], "isCareerPlannerEnabled": false, "positions": [{"locations": ["Tucson, AZ"], "t_update": 1638500570, "job_description": "Responsibilities: Accountable for identifying, planning, and tracking documentation deliverables according to the Product Development Process (PDP) and Quality System processes. Participates in project planning and advises project leadership on best practices, tailoring of deliverables, timelines, and risks for the given project type. Facilitates technical, documentation and release review meetings. Drives completion of action items. Coordinates with cross functional team members (Quality, Architecture, Requirements, Development, Test, Support, etc.) to monitor deliverable status, and drives timely approvals per project schedule. Updates articles in the department wiki. Ensures that documentation deliverables adhere to correct templates and versions according to current Quality System processes. Has subject matter expertise on Product Development Processes and Work Instructions. Manages and maintains Software Design History Files (DHF) in the Document Control System. Manages change workflows via the Document Control System (DCS). Other duties as assigned by management. Knowledge, Skill or Ability Req Pref Proficiency Ability to create project documentation that is complete, consistent, and accurate. Ability to plan project components and effectively report status to stakeholders. Familiar with product development processes. Familiarity with electronic document control systems. Strong organizational skills. Strong written and verbal communication skills. Familiarity with project management tools. Ability to use established procedures, policies and methodologies to resolve standard problems.", "t_create": 1638499596, "id": 137449139903, "ats_job_id": 137449139903, "name": "Software Project Coordinator", "display_job_id": 137449139903, "business_unit": "Unknown", "medallionProgram": null, "hot": 0, "location": "Tucson, AZ", "stars": 0, "department": null, "type": "ATS"}, {"locations": ["Tucson, AZ"], "t_update": 1638499473, "job_description": "Responsibilities Manages clinical testing and lab services projects from initiation through contract completion in collaboration with Specialist Senior or Program Manager. Performs tactical coordination of timelines for all projects and functions within CDx Pharma Services and: Develops project plans, establish and coordinates timelines for assigned projects and functions. \\ Manages execution of crossfunctional plans and tracks progress of activities \\ Identifies gaps, potential bottlenecks or delays and challenge assumptions \\ Proposes options to close gaps and get projects back on track. Oversees and guides day to day activities of sample process flow and accurate reporting of results. Implements / pulls in best practices within the clinical sciences team; fosters continuous improvement by ensuring knowledge and experience exchange. Guides and manages crossfunctional interactions to complete the assigned projects within the deadline. Interface with resources outside of the company (Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serves as single point of contact with Pharma and Roche clients. Manages meeting activities such as setting agendas, organizing meeting time and editing meeting minutes. Tracks, maintains and communicates project reports and clinical study data to Pharma and Roche clients. Performs miscellaneous duties and special projects as assigned Other duties as assigned by management. Knowledge and Skills Proficiency with word processing, spreadsheet, database and email software (e.g., Microsoft Excel, Microsoft Word). Possesses interpersonal skills and ability to work in a team environment. Displays leadership skills. Ability to work under time pressure while maintaining high standards of precision and data quality. Ability to manage projects with activity/milestone achievement to complete clinical study testing and data reporting to pharma partners. Ability to apply specialized knowledge and skills in the functional areas, particularly interfacing with laboratory, scientific, and medical staff. Beginning November 15, 2021, Roche requires all US based contractors to be fully vaccinated against COVID19 as of their start date. This requirement is a condition of contractor assignment at Roche, and it applies regardless of whether the position is located at a Roche campus or is fully remote. If you are unable to receive the vaccine due to a disability or serious medical condition, or because it is prohibited as a result of your sincerely held religious beliefs, you will have an opportunity to request a reasonable accommodation.", "t_create": 1638499157, "id": 137449139900, "ats_job_id": 137449139900, "name": "Clinical Sciences Specialist I", "display_job_id": 137449139900, "business_unit": "Unknown", "medallionProgram": null, "hot": 0, "location": "Tucson, AZ", "stars": 0, "department": null, "type": "ATS"}, {"locations": ["Indianapolis, IN"], "t_update": 1638498866, "job_description": "The OffSite Implementation Center (OSIC) Field Service Installation Technician will be responsible for the setup and delivery of equipment ready for onsite installation at customer sites and according to the preinstallation process. Set up and operate equipment and processes in accordance with standard operating procedures and site protocols. Inspect product for quality and adherence to specifications. Completes and ensures accuracy of all process orders and associated required documentation, records, and metrics. Prepare and maintain work centers according to specifications. May train others in the department as needed. Responsible for maintaining and continuously improving the quality system and achieving quality objectives through daily actions. Skills 2 years progressive experience repairing or servicing mechanical/system hardware and software, or networking/wireless networking or equivalent military experience Effective timemanagement, organization and prioritization skills. Good written/verbal communication skills Detail oriented and ability to work in a fastpaced environment, both independently and within a team setting Advanced knowledge of electronics, electromechanical systems, and information technology and/or certified Medical Technician Preferred Valid forklift operator certificate or ability to obtain a forklift operator certificate. Roche will provide certification training Ability to understand and comply with appropriate safety, health, and environmental procedures Preferred: Experience working in a Lean Manufacturing environment Preferred: Experience working in a regulated work environment Education Required; High school diploma or GED Required; 2 years of technical school or equivalent military training or equivalent work experience Preferred; Bachelors Degree \ufeffRoche USA now requires all workers, whether onsite or remote to be fully vaccinated by 11/15/21. Exceptions will be given on a case by case basis only for medical.", "t_create": 1638497504, "id": 137449139817, "ats_job_id": 137449139817, "name": "Field Service Technician", "display_job_id": 137449139817, "business_unit": "Unknown", "medallionProgram": null, "hot": 0, "location": "Indianapolis, IN", "stars": 0, "department": null, "type": "ATS"}, {"locations": ["Vacaville, CA"], "t_update": 1638497026, "job_description": "Description: Conducts routine and nonroutine laboratory equipment maintenance. Performs sample management maintenance including but not limited to raw materials, inprocess items, finished product and stability program according to established operating procedures. Revises and updates standard operating procedures as needed. May perform special projects on analytical and instrument problem solving. Participates in the preparation of investigations, summaries and reports. Job Responsibilities Perform routine and semiroutine assignments that are complex in support of lab operations: Perform maintenance on Laboratory equipment in support of laboratory operations Exhibit detail oriented documentation skills to ensure RightFirstTime operations Identify and support resolution of technical problems Coordinate with customers to support operation activities Prepare basic and complex reagents as assigned. Create and maintain finite schedules. Create and maintain work in progress tracking tool. Receive and provide training. Identify discrepancies, participate in quality investigations and CAPA (corrective actions preventive actions) initiative as needed Actively participate in group and project teamwork; project and process improvement. Good understanding of global systems and cGMP Compliance requirements/regulations Assist in preparing for internal and external inspections by ensure Laboratory is inspection ready at all times. Ability to create/revise lab associated documents e.g. testing procedures, FNs, SOPs. Perform other duties as requested by managers to support Quality activities Important: Genentech has mandated COVID19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services to Genentech are required to comply with this requirement. If you are unable to receive the vaccine due to a disability or serious medical condition, or because it is prohibited as a result of your sincerely held religious beliefs, you will have an opportunity to request a reasonable accommodation.", "t_create": 1638496923, "id": 137449139791, "ats_job_id": 137449139791, "name": "Sr QC Analyst ", "display_job_id": 137449139791, "business_unit": "Unknown", "medallionProgram": null, "hot": 0, "location": "Vacaville, CA", "stars": 0, "department": null, "type": "ATS"}, {"locations": ["South San Francisco, CA"], "t_update": 1638496781, "job_description": "The candidate will maintain, operate, and troubleshoot LCMS/MS instruments, automated liquid handlers, and related laboratory equipment used to prepare and analyze the protein samples. The candidate is expected to perform the MAM data analysis, summarize and write the development technical reports. The candidate will closely work with analysts in GMP lab for implementation, training and method transfer. Requirements Ph.D. or Master's degree in Analytical Chemistry, Biochemistry, Mass Spectrometry, or related technical field. Handson experience in chromatography and mass spectrometry analysis of proteins, particularly with developing and implementing LCMS methods using high resolution instruments for MS/MS, peptide mapping, posttranslational modifications, etc. Ability to keep accurate and timely documentation per departmental guidelines, timely document and communicate abnormal laboratory observations. Highly motivated, achievementoriented, attention to detail, wellorganized, team player, with excellent troubleshooting and problemsolving skills for MS analytical workflows. Good oral and written communication skills are preferred. Important: Genentech has mandated COVID19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services to Genentech are required to comply with this requirement. If you are unable to receive the vaccine due to a disability or serious medical condition, or because it is prohibited as a result of your sincerely held religious beliefs, you will have an opportunity to request a reasonable accommodation.", "t_create": 1638496587, "id": 137449139784, "ats_job_id": 137449139784, "name": "Scientist", "display_job_id": 137449139784, "business_unit": "Unknown", "medallionProgram": null, "hot": 0, "location": "South San Francisco, CA", "stars": 0, "department": null, "type": "ATS"}, {"locations": ["South San Francisco, CA"], "t_update": 1638496294, "job_description": "Description: We are seeking a highly motivated individual to join the department of Protein Analytical Chemistry (PAC) (within PTDU) as a Contractor. A successful candidate will be expected to work handson in the laboratory to generate analytical data in support of the pipeline and technical development projects. This will include analytical characterization and testing as well as development and execution of analytical methods. The candidate may also collaborate with cross functional colleagues and contribute to manufacturing process development and clinical trial and commercializationenabling regulatory filings (e.g. BLAs and INDs). Requirements: A BS or MS in biological or chemical sciences, or related disciplines with 0 to 2+ years of relevant experience. Strong technical and handson lab skills; ability to quickly acquire new technical skills; experience working in research labs or industrial internships is highly desirable. Ability to follow and execute experimental protocols and test procedures as well as follow verbal or written instructions. Ability to work independently or under minimal supervision to design and conduct experiments, as well as, interpret, document, and communicate results. Ability to work safely in the laboratory, following all environmental health and safety requirements. Exceptional written and verbal communication skills, highly selfmotivated, eager to work in a dynamic and fastpaced environment, and be capable of handling multiple tasks while meeting timelines. Strong collaborative skills and a passion for working in a multidisciplinary project team environment. Familiarity with various traditional analytical methods for protein characterization, such as CE, HPLC or mass spectrometry, is helpful but not required. As needed, the candidate will be expected to learn new methods (based on provided training) and with time, become proficient in execution and troubleshooting. Prior experience with characterization of recombinant monoclonal antibodies or other protein therapeutics is helpful but not required. Important: Genentech has mandated COVID19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services to Genentech are required to comply with this requirement. If you are unable to receive the vaccine due to a disability or serious medical condition, or because it is prohibited as a result of your sincerely held religious beliefs, you will have an opportunity to request a reasonable accommodation.", "t_create": 1638495725, "id": 137449139775, "ats_job_id": 137449139775, "name": "Sr Research Associate", "display_job_id": 137449139775, "business_unit": "Unknown", "medallionProgram": null, "hot": 0, "location": "South San Francisco, CA", "stars": 0, "department": null, "type": "ATS"}, {"locations": ["South San Francisco, CA"], "t_update": 1638495633, "job_description": "Description: Important: Genentech has mandated COVID19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services to Genentech are required to comply with this requirement. Delivery Manager, Paid Media [Contractor] The contractor role, Delivery Manager, Paid Media reports to the Team Lead and is accountable for delivering highquality, timely, and efficient digital customer experiences through paid media and social placements within Digital Engagement & Delivery Team as part of Experience Operations (XO). Digital Engagement and Delivery is composed of experienced digital experts who partner across Commercial, Medical and Government Affairs (CMG) to orchestrate and deliver integrated digital customer experiences that drive measurable business outcomes. This role is based in South San Francisco, but is open to fully remote contractor candidates who are willing to travel up to South San Francisco at times. Key Responsibilities: Drives customer and patientcentric media service delivery, optimization for impact and efficiency Creates project plans and ensures key milestones, dependencies and timelines are proactively communicated across stakeholders and partners Partners with the marketing team to translate marketing messaging and strategy into integrated, omnichannel marketing strategies and tactics that support and drive the business goals of the brand and organization. Works closely with agency partners to analyze, track, optimize, and update media programs across all channels Leverages internal analytics and external data to support insights and businessfocused recommendations Understands the interplay between paid media, social media, email, and Website touchpoints and can speak to the role each plays across the customer and patient journey. Has a knack for developing and maintaining relationships with key stakeholders across a large, global, and highly matrixed organization. Delivers operational excellence by identifying and implementing process improvements and informing standards that enable great customer experience Designs and delivers quality production by adhering to XO processes and standards Seeks opportunities to optimize, test pilots, or advance new capabilities and share learnings across XO and the broader enterprise Skills Domain expertise in multichannel digital marketing and deep familiarity with paid media and social media marketing technology, processes, and tools Ability to apply data and analysis to drive decision making Strong planning, critical thinking and problemsolving skills to meet goals within the constraints of time and budget Bias for action, strong sense of immediacy, and drive to achieve objectives Adept at vendor/agency management to maintain healthy partnerships and deliver operational excellence Learning mindset and ability to identify/apply learning to other situations QUALIFICATIONS Bachelor's degree 7+ years experience working in digital/software marketing, digital production, marketing technology, or marketing operations related functions Pharma experience or experience in a highly regulated industry is a plug 5+ years of significant focus on paid media and social media Experience in the pharmaceutical, biotech or healthcare industry This is a contractor role and the individual in this role will be employed by a third party, not by Genentech", "t_create": 1638495536, "id": 137449139773, "ats_job_id": 137449139773, "name": "Paid Media Delivery Manager", "display_job_id": 137449139773, "business_unit": "Unknown", "medallionProgram": null, "hot": 0, "location": "South San Francisco, CA", "stars": 0, "department": null, "type": "ATS"}, {"locations": ["South San Francisco, CA"], "t_update": 1638495288, "job_description": "Description: We have a contract position opening for a talented Research Associate to join our Biochemical and Cellular Pharmacology Department within Genentech's Research and Early Development (gRED) organization. The successful candidate will support biochemical and cellbased functional characterization of protein therapeutics for immunooncology. More specifically, the individual will develop, validate and execute biochemical and cellbased assays to characterize and screen biologic therapeutics in vitro and support leadfinding/optimization efforts. In addition, the candidate will function as part of a multidisciplinary project team that will coordinate with Cancer Immunology, Antibody Engineering, and Protein Chemistry groups to advance lead molecules of the projects. Who You Are B.S. or M.S. degree in Immunology, Biochemistry, Cell Biology, or a related field with experience in academia, biotechnology and/or pharmaceutical industry More than 1year mammalian cell culture and cell based assay experience is a must. Practical experience in the design, development, validation and execution of biochemical and cellbased assays Ability to work independently to design, execute, and interpret experiments, and also collaborate with project teams Excellent teamwork, communication, time management, and organizational skills Additional desirable skills A strong foundation in immunology and handson expertise in immune cell assays Experience with flow cytometry Experience with primary immune cell isolation and culture Familiarity with automated or semiautomated instrumentation Important: Genentech has mandated COVID19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services to Genentech are required to comply with this requirement.", "t_create": 1638495156, "id": 137449139750, "ats_job_id": 137449139750, "name": "Research Associate", "display_job_id": 137449139750, "business_unit": "Unknown", "medallionProgram": null, "hot": 0, "location": "South San Francisco, CA", "stars": 0, "department": null, "type": "ATS"}, {"locations": ["South San Francisco, CA", "Remote"], "t_update": 1638495036, "job_description": "Important: Genentech has mandated COVID19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services to Genentech are required to comply with this requirement. If you are unable to receive the vaccine due to a disability or serious medical condition, or because it is prohibited as a result of your sincerely held religious beliefs, you will have an opportunity to request a reasonable accommodation. Description: The Human Genetics group at Genentech is seeking to engage a contractor with a computational and genetics background to implement advanced statistical methods and pipelines that deliver innovative analysis of largescale genetic datasets. This work will be carried out under the supervision of Scientists from Human Genetics. Relevant focus areas include methods involved in analysis of GWAS and functional genomic data, and the analysis of genenetworks and pathways. Skills The candidate should have experience programming in UNIX, bash/other scripting languages & R/python. They should have a detailed understanding of human genetics and/or genomics, and experience handling and analyzing genomescale data. The contractor should have experience working with high performance computing and be able to produce highquality output with minimal supervision. Experience working with longitudinal analyses using logistic and linear regression, survival analyses and repeated measures analyses would be a strong plus. Education Applicants should have completed a PhD in Computational Biology, Human Genetics, Computer Science, Biostatistics, or related fields. Additional postdoctoral experience is a major plus. This position would be available for a year and can be held remotely.", "t_create": 1638494790, "id": 137449139728, "ats_job_id": 137449139728, "name": "Bioinformatics Associate I", "display_job_id": 137449139728, "business_unit": "Unknown", "medallionProgram": null, "hot": 0, "location": "South San Francisco, CA", "stars": 0, "department": null, "type": "ATS"}, {"locations": ["Vacaville, CA"], "t_update": 1638494604, "job_description": "Description: Contractor is responsible for supporting gantenerumab tech transfer and tocilizumab commercial process monitoring. Tech transfer activities include review of manufacturing specifications against process descriptions and characterization reports to ensure successful engineering and qualification runs at large scale. Process monitoring activities include compilation and analysis of cell culture data to ensure consistent performance of commercial production. Skills Preferred: Working experience in cGMP biopharmaceutical production setting (process development and/or manufacturing technical support). Knowledge of Process Validation approaches, industry practice, and applicable regulations and guidance and MP documentation requirements. Knowledge with statistical methods (e.g. Design of experiments, and multivariate data analysis techniques) Knowledge with OSisoft, Inc., PI Server and client tools, Oracle server and client tools, Microsoft Visual Studio, Visual Basic, SQL, SAS JMP and associated scripting language Education To be eligible for this position, contractor must have completed BS or higher degree at an accredited college or university and proficiency in data acquisition and programing techniques, and strong technical writing and oral communication skills. Important: Genentech has mandated COVID19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services to Genentech are required to comply with this requirement. 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