{"data":[{"id":"519365","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eMedical, Dental and Vision Insurance\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eBasic Life, AD\u0026amp;D, Short- and Long-Term Disability Insurance\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e401k with Company Match up to 4%\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCompany Equity\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eGenerous Paid Time Off including 18 Company Holidays (with a summer and winter shutdown), Vacation, and Wellness Time\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAnnual Lifestyle Account for reimbursement of fitness programs, equipment and more\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEmployee Stock Purchase Program (ESPP)\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eFlexible Spending Accounts (Commuter/Parking, Dependent Care \u0026amp; Healthcare)\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStudent Debt Program (Company Contribution to Loans)\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMental Health Wellness Program\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSubsidized onsite lunch program\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOnsite Gym Facilities\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePaid Parental Leave\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003eAnd More!\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Job Benefits","compensation":"$165,000 - $185,000 / year","compensation_minimum":165000.0,"compensation_maximum":185000.0,"compensation_currency":"USD","compensation_frequency":"year","compensation_visible":true,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eWe are seeking a highly experienced and innovative Process Engineer to support process development activities for Codexis’ Enzyme Catalyzed Oligonucleotide (ECO) Synthesis® manufacturing platform, driving innovation and scalability from bench to GMP production. This role is pivotal in advancing sustainable oligonucleotide manufacturing technologies that disrupt traditional chemical synthesis methods and meet stringent quality and regulatory standards.\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eIf any of the below describes you, we would love to meet you!\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003ePossess a passion for being part of the therapeutic community helping bring cutting edge treatments to patients in need.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnjoys collaboration across different functional groups to get a holistic understanding of process development along with aligning data with internal stakeholders.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnjoys problem solving by implementing engineering and analytical solutions.\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProviding technical leadership in hands‑on process development, applying advanced engineering principles to drive the design, build‑out, and maturation of the ECO Synthesis® platform in close partnership with cross‑functional development teams\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eLeading the scale‑up strategy for the ECO Synthesis® platform, ensuring process is robust, well‑characterized, and ready for transition into a cGMP manufacturing environment.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eChampioning laboratory safety, maintaining a clean and compliant workspace, conducting process hazard analyses and risk assessments, and ensuring safe working environment for all team members.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOverseeing documentation quality, ensuring batch records, SOPs, and development reports meet GDP standards; providing mentorship and guidance to early‑career engineers and scientists on documentation and experimental/statistical rigor.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eLeading the development and delivery of key technical work, including internal and external presentations, detailed technical reports, and comprehensive technology transfer packages for siRNA manufacturing processes.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOwning the creation of engineering design tools, including mass and energy balances, process flow diagrams (PFDs), equipment specifications, and cost models to support scale‑up, facility integration, and long‑term platform deployment.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eServing as primary technical liaison with external vendors, driving equipment selection, qualification, and support activities essential for effective process development and scale‑up.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e• Bachelor’s degree in Chemical Engineering, Biochemical Engineering, or related field with 10+ years of relevant industrial experience, or M.S. with 8+ years.\u003cbr\u003e• Expertise in flow chemistry, biocatalysis, or oligonucleotide synthesis technologies (e.g., SPOS, enzymatic platforms).\u003cbr\u003e• Demonstrated leadership in scale‑up activities, including tech transfer of biocatalytic or nucleic acid–based processes from laboratory to pilot or commercial manufacturing environments.\u003cbr\u003e• Proficiency in process modeling and simulation tools such as Aspen Plus, SuperPro Designer, COMSOL, or DynoChem; and proficient with data analytics or scripting tools (e.g., R, JMP, Python).\u003cbr\u003e• Strong leadership, communication skills, with the ability to collaborate effectively across cross-functional teams including R\u0026amp;D, Operations, Quality, and Engineering.\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003eAdditional experience that would be valuable for this role includes:\u003c/strong\u003e\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e• Prior experience managing early career engineers, scientist, or research associates.\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e• Expertise in purification technologies, such as chromatography, filtration, or enzyme/oligonucleotide purification workflows.\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e• Experience with facility design or equipment specification, for nucleic acid manufacturing.\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e• Deep understanding of quality systems and regulatory expectations, including ISO-based quality frameworks and GMP principles.\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","skills_knowledge_expertise_header":"Skills, Knowledge \u0026 Expertise","title":"Principal Process Engineer, ECO Synthesis","url":"https://codexis.pinpointhq.com/en/postings/c90e4921-af0f-4252-ac02-93eee5cf24d4","path":"/en/postings/c90e4921-af0f-4252-ac02-93eee5cf24d4","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"525365","requisition_id":"CDX-DPT-GR-0293","department":{"id":"77600","name":"46 - Process Engineering"},"division":null,"structure_custom_group_one":null},"location":{"id":"10326","city":"Redwood City","name":"Redwood City, CA","postal_code":"75024","province":"California"}},{"id":"519381","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eMedical, Dental and Vision Insurance\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eBasic Life, AD\u0026amp;D, Short- and Long-Term Disability Insurance\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e401k with Company Match up to 4%\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCompany Equity\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eGenerous Paid Time Off including 18 Company Holidays (with a summer and winter shutdown), Vacation, and Wellness Time\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAnnual Lifestyle Account for reimbursement of fitness programs, equipment and more\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEmployee Stock Purchase Program (ESPP)\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eFlexible Spending Accounts (Commuter/Parking, Dependent Care \u0026amp; Healthcare)\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStudent Debt Program (Company Contribution to Loans)\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMental Health Wellness Program\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSubsidized onsite lunch program\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOnsite Gym Facilities\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePaid Parental Leave\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003eAnd More!\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Job Benefits","compensation":"$128,000 - $142,000 / year","compensation_minimum":128000.0,"compensation_maximum":142000.0,"compensation_currency":"USD","compensation_frequency":"year","compensation_visible":true,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eThe Scientist I is a part of the Process Chemistry department and responsible for process design and optimization for enzymatic synthesis of therapeutic RNA oligonucleotides using immobilized enzymes. The process development team within Process Chemistry is developing a cutting-edge synthesis technology for the generation or RNAi based compounds. The individual will have the opportunity to pioneer novel processes while developing enzymatic and oligonucleotide skill sets. 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Successful candidates will be a part of a dynamic and enthusiastic team responsible for development, scale up and tech transfer of the ECO Synthesis™ platform. The individual will be working with a high performing team with day-to-day laboratory workflows and operations helping design, optimize, and analyze workups from the ECO Synthesis™ platform. The position is an on-site role located at our Redwood City facility\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cbr\u003eIf any of the below describes you, we would love to meet you!\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003ePossess a passion for being part of the therapeutic community helping bring cutting edge treatments to patients in need.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnjoys collaboration across different functional groups to get a holistic understanding of process development along with aligning data with internal stakeholders.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnjoys problem solving by implementing engineering and analytical solutions.\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eEstablishing and executing scientific experimentation plans for ECO Synthesis™ with scientists in the process development team.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eGenerating Design of Experiments (DoE) models, executing laboratory workflows and compiling data into the design space.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eIdentifying critical process parameters that can be improved and proposing solution-based applications from data driven analysis. \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePresenting data at team and cross functional level on the current PD ongoings.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eProviding routine troubleshooting and maintenance of process development instruments including reactors, HPLCs, purification skids and UF/DF manifolds.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"","skills_knowledge_expertise":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eBachelor’s degree in Chemistry, Chemical Engineering, Biology, Biochemistry or relevant scientific field and 4 years of relevant industrial/academic experience in a laboratory environment OR Master’s degree in Chemistry, Chemical Engineering, Biology, Biochemistry or relevant scientific field and 2 years of hands on experience.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to learn quickly, prioritize responsibilities, multi-task, think critically, and work both independently and within teams in a fast-paced environment.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eExperience with documentation, record keeping, writing SOPs and reports.\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u0026nbsp;\u003cstrong\u003eAdditional experience that would be valuable for this role includes:\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eHands-on experience working with laboratory scale bioreactors, laboratory automation, HPLC, TFF, or preparatory scale purification.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eGeneral knowledge of biochemistry and protein expression concepts.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUnderstanding of DoE based applications and generating of design spaces.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eExperience with statistical modeling software such as JMP.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","skills_knowledge_expertise_header":"Skills, Knowledge \u0026 Expertise","title":"Research Associate III, Process Development ","url":"https://codexis.pinpointhq.com/en/postings/438e8330-e03a-4c35-b936-4d41fb2c03fc","path":"/en/postings/438e8330-e03a-4c35-b936-4d41fb2c03fc","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"530509","requisition_id":"CDX-DPT-GR-0292","department":{"id":"21436","name":"55 - 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Successful candidates will be a part of a dynamic and enthusiastic team dedicated to supporting Codexis product development through analytical development. The individual will be working with a high performing team with day-to-day laboratory workflows and operations to help with analytical method development, validation, and transfer. The position is an on-site role located at our Redwood City facility.\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eEstablishing and executing scientific experimentation plans for analytical method development with scientists on the analytical development team.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform data processing, evaluation and interpretation of experimental data, drawing conclusions based on the results.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform analytical testing of finished products and development samples.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eParticipate in analytical activities including method development, validation, and various analytical studies.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePresent data at team and cross functional level on the current AD ongoings.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform overall lab support functions including routine maintenance of analytical instruments, ordering and maintaining inventory of sample, reagents and lab supplies.\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e•\tBS in Analytical Chemistry, Biochemistry or Biology science or relevant scientific field with a minimum of 6 years of relevant industrial/academic experience in a laboratory environment, OR Master’s degree and 4 years of relevant industrial/academic experience in a laboratory environment.\u003cbr\u003e•\tAbility to learn quickly, prioritize responsibilities, multi-task, think critically, and work both independently and within teams in a fast-paced environment.\u003cbr\u003e•\tPrior working experience with HPLC-UV-MS, UV-Vis, ELISA and CE-SDS. \u003cbr\u003e•\tWorking knowledge and experience with good documentation practices.\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003eAdditional experience that would be valuable for this role includes:\u003cbr\u003e\u003c/strong\u003e\u003cbr\u003e•\tKnowledge of ICH Quality Guidelines related to analytical method development and validation, impurities and stability.\u003cbr\u003e•\tGeneral knowledge of oligonucleotide, biochemistry and enzyme science.\u003cbr\u003e•\tUnderstanding of systematic study design and conception.\u0026nbsp;\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e","skills_knowledge_expertise_header":"Skills, Knowledge \u0026 Expertise","title":"Research Associate IV, Attribute Sciences","url":"https://codexis.pinpointhq.com/en/postings/dda4e074-6bbb-452e-a7b6-fcd965b5282f","path":"/en/postings/dda4e074-6bbb-452e-a7b6-fcd965b5282f","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"533769","requisition_id":"CDX-DPT-GR-0299","department":{"id":"21436","name":"55 - ECO Process Development"},"division":null,"structure_custom_group_one":null},"location":{"id":"10326","city":"Redwood City","name":"Redwood City, CA","postal_code":"75024","province":"California"}},{"id":"528604","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eMedical, Dental and Vision Insurance\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eBasic Life, AD\u0026amp;D, Short- and Long-Term Disability Insurance\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e401k with Company Match up to 4%\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCompany Equity\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eGenerous Paid Time Off including 18 Company Holidays (with a summer and winter shutdown), Vacation, and Wellness Time\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAnnual Lifestyle Account for reimbursement of fitness programs, equipment and more\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEmployee Stock Purchase Program (ESPP)\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eFlexible Spending Accounts (Commuter/Parking, Dependent Care \u0026amp; Healthcare)\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStudent Debt Program (Company Contribution to Loans)\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMental Health Wellness Program\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSubsidized onsite lunch program\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOnsite Gym Facilities\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePaid Parental Leave\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003eAnd More!\u003c/div\u003e","benefits_header":"Job Benefits","compensation":"$160,000 - $180,000 / year","compensation_minimum":160000.0,"compensation_maximum":180000.0,"compensation_currency":"USD","compensation_frequency":"year","compensation_visible":true,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eThe Senior Manager, Maintenance \u0026amp; Calibration will lead the development, implementation, and execution of maintenance and calibration programs for the GMP manufacturing facility.\u0026nbsp; This role is hands-on during facility startup, supporting commissioning and qualification (C\u0026amp;Q) activities, and will transition into building and leading a high-performing maintenance organization responsible for ongoing GMP compliance, asset reliability, and continuous improvement. This position will be based in Hayward, CA at our Huntwood Facility.\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003eIf any of the below describes you, we would love to meet you! \u003c/strong\u003e\u003cbr\u003e•\tStrong technical leader with the ability to operate at both strategic and hands-on levels\u003cbr\u003e•\tExperience supporting startup, commissioning, and GMP qualification activities\u003cbr\u003e•\tProven ability to build maintenance programs from the ground up\u003cbr\u003e•\tCollaborative leader capable of integrating with Facilities, Manufacturing, QC, and Engineering teams\u003cbr\u003e•\tContinuous improvement mindset with focus on reliability, uptime, and compliance\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e•\tServe as a core team member supporting facility startup, commissioning, and operational readiness\u003cbr\u003e•\tSupport development and execution of commissioning plans, qualification protocols and reports, turnover packages, and system walkdowns\u003cbr\u003e•\tDesign, implement, and scale a GMP-compliant maintenance and calibration program\u003cbr\u003e•\tEstablish and maintain a Computerized Maintenance Management System (CMMS)\u003cbr\u003e•\tDevelop maintenance and calibration SOPs, job plans, intervals, and standard work instructions\u003cbr\u003e•\tEnsure maintenance and calibration requirements are embedded in system design and project turnover\u003cbr\u003e•\tDevelop spare parts strategies, critical equipment lists, and asset hierarchies\u003cbr\u003e•\tDevelop and execute preventive, predictive, and corrective maintenance programs to maximize reliability and uptime\u003cbr\u003e•\tCoordinate contractor and vendor activities for maintenance and calibration services\u003cbr\u003e•\tRecruit, train, and mentor maintenance staff while fostering a safety-first, GMP-compliant culture\u003cbr\u003e•\tPartner with cross-functional teams to support facility modifications and manufacturing operations\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e•\t10+ years of experience in maintenance, reliability, or facilities engineering in a GMP or regulated environment\u0026nbsp;\u003cbr\u003e•\tDirect experience supporting facility startup, commissioning, and qualification\u0026nbsp;\u003cbr\u003e•\tStrong knowledge of GMP / GDP requirements, equipment qualification (IQ/OQ/PQ) and CMMS systems and maintenance program development\u003cbr\u003e•\tExperience managing utilities and process equipment (e.g., HVAC, clean utilities, process skids)\u0026nbsp;\u003cbr\u003e•\tDemonstrated ability to lead teams and cross-functional initiatives\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e","skills_knowledge_expertise_header":"Skills, Knowledge \u0026 Expertise","title":"Senior Manager, Maintenance \u0026 Calibration","url":"https://codexis.pinpointhq.com/en/postings/85903a3f-16d0-4225-a32f-82f6fa890ae6","path":"/en/postings/85903a3f-16d0-4225-a32f-82f6fa890ae6","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"533800","requisition_id":"CDX-DPT-GR-0301","department":{"id":"78370","name":"63 Facilities Operations"},"division":null,"structure_custom_group_one":null},"location":{"id":"88762","city":"Hayward","name":"Huntwood, CA","postal_code":"94544","province":"California"}}]}