{"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 Magnit Global", "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/1670426473::magnit-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": "<b>Magnit Direct Sourcing</b> powered by Magnit Global & eightfold.ai</a> </p>", "page-footer-text": "powered By"}, "hideJobCart": false, "recaptcha_enabled": 0}, "positions": [{"id": 137454617426, "name": "Contracts Manager IV", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1680046448, "t_create": 1680042519, "ats_job_id": 137454617426, "display_job_id": 137454617426, "type": "ATS", "id_locale": "137454617426-en", "job_description": "Expertise in the processes, systems, and tools that support various contracting-related activities is critical to the success of this position. Scientific/Business Degree, BA or BS; J.D. or Paralegal Certification preferred 5 or more years relevant experience in pharmaceutical/biotechnology, preferably in Medical Affairs, contract management, or project management Working knowledge and experience of drug development/medical affairs, product development, drug commercialization and/or healthcare/market landscape Demonstrate flexibility and an agile mindset - able to adapt in a regularly changing environment Strong problem-solving capabilities and skills. Has demonstrated the ability to anticipate and solve problems of moderate complexity and scope e.g. evaluate, interpret and present complex data Strong interpersonal, partnering and influencing skills; can effectively and quickly establish rapport with all partners and stakeholders and influence without authority Excellent communication and presentation skills, highly effective at summarizing information and tailoring messages towards specific audiences Strong business acumen: ability to integrate knowledge of pharmaceutical industry and drug development in development of strategy and plans, key competitors and marketplace factors/dynamics and assess impact to strategy, plans, activities Ability to effectively influence business terms and financial costs Enterprise mindset: dedication to acting on behalf of the whole company, not just the group being supported - Proficiencies with various project management systems and software/programs is a plus Proven ability to manage multiple tasks to conclusion, on time and without compromising quality Track record of effectively working within a highly matrixed organization and cross functional teams and collaborating with others internally and externally Business travel, by air or car as required for regular internal and external business meetings Ability to embrace and believe in Genentech's operating principles Enable Business Owners to accelerate execution of projects by reducing the burden of navigating through the contracts process Implement the overarching BSO strategies, plans, objectives, standards and practices in alignment with business needs to deliver operational excellence within USMA Manage tracking of contracts and purchase orders that enables Business Owners to maintain line-of-sight to their projects or business Manage business process navigation (contract management, drug safety language, MC-FMV process, iHCP process, etc.), provide guidance and support to USMA while mitigating legal risk", "stars": 0.0, "medallionProgram": null, "location_flexibility": null}, {"id": 137454583941, "name": "Safety Scientist II", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1679616874, "t_create": 1679614444, "ats_job_id": 137454583941, "display_job_id": 137454583941, "type": "ATS", "id_locale": "137454583941-en", "job_description": "Under the matrix leadership of the SSL and in collaboration with PCS colleagues \u25cf Develop and maintain an understanding of the safety profile of their assigned product(s) or therapy areas. Develop and maintain an expert understanding of the safety profile of the assigned product(s) as well as understanding of the relevant strategic context (e.g., disease under study, safety profile of competitors, mechanism of action) \u25cf Responsible for individual and aggregate case reporting activities including ICSR case management (medical review) and aggregate reporting (i.e. DSUR, PBRER) \u25cf Responsible for signal detection and management activities including, but not limited to STAR maintenance, ISMP maintenance. Contribute to the strategy and review of safety assessments and drug safety reports for signals or issues (inc, product quality) or in response to Regulatory Authority requests \u25cf Contribute to the development of the product safety strategy and provide drug safety input into the Clinical Development strategy \u25cf Contributing to risk management activities including preparation and maintenance of CCDS, labeling document maintenance (including the IB), risk communications, RMP, REMS \u25cf Contributing to study management from a safety perspective through SMT/PET activities and document review and maintenance across the development continuum (early phase to post marketing studies), including PASS \u25cf Contribute to regulatory authority submissions (Investigational New Drug/IND applications, New Drug Applications/NDAs, Marketing Authorization Applications/MAAs, Variations, Renewals, etc.) by reviewing safety data and preparing relevant sections of the filing and submission packages in consultation with SPL \u25cf Responsible for the preparation and maintenance of safety sections of the Company Core Data Sheet and/or Reference Safety Information in the IB \u25cf Participate in and provide input for Drug Monitoring Committees (iDMC) or internal monitoring committee (IMC) meetings, as applicable \u25cf In partnership with the SSL, support presentation of important safety issues to the Drug Safety Committee (DSC), Development Review Committee (DRC) and other internal and external review and governance committees as needed. \u25cf Author or contribute to scientific publications (abstracts, posters, papers) for scientific meetings/journals \u25cf Acts independently to manage safety responsibilities on study teams and in activities supporting safety science \u25cf Take on the responsibility for specialized roles with PCS. These may include, but are not limited to; functional business process owner, subject matter expert. \u25cf Demonstrates independence and high competence in the conduct of all safety science responsibilities \u25cf Develop and maintain knowledge of the pharmaceutical industry and drug development, including a comprehensive knowledge of pharmacovigilance activities and requirements \u25cf Understands how safety activities contribute to company development and commercialization goals and takes measures to maximize safety value to the organization \u25cf Establish and maintain collaborative working relationships with all key stakeholders, and internal and external customers and ensure the same across relevant teams \u25cf Responsible for coordination and collaboration with vendors servicing Safety Science \u25cf Acts independently and with minimal supervision to manage safety responsibilities on study teams and in activities supporting safety science \u25cf Trains and mentors more junior PCS scientists \u25cf Proactively takes on responsibility for more complex deliverables \u25cf Takes on team leadership responsibility in order to manage and complete medium and high priority projects \u25cf Seen by peers and cross-functional colleagues as expert in some safety science activities \u25cf Willing to challenge embedded behaviors/mindsets, in order to bring new and agile approaches to ways of working, and/or to improve quality and efficiency. \u25cf Holds themselves and peers accountable for their behaviors and actions. \u25cf Minimum Qualifications: Qualified healthcare professional or Life Sciences graduate. \u25cf Preferred Qualifications: A relevant postgraduate qualification (e.g. PHD/MSc in a Life sciences discipline; PharmD or other post-graduate health professional qualifications) would be advantageous. \u25cf Understanding of GxP and regulated processes and end to end clinical trial lifecycle \u25cf Strong orientation towards process improvement and cross-functional teamwork \u25cf Effectively work with remote partners on a global team \u25cf Excellent communication skills, both written and verbal \u25cf Apply complex data analysis / statistical methods to evaluate, interpret and present scientific data with clarity \u25cf Strong presentation skills, effective at summarizing and presenting the key considerations and decision points \u25cf Ability to effectively train others on departmental practices and processes \u25cf Application of project management methodology This is the pay range that Magnit reasonably expects to pay for this position: $79.14/hour-$105.51/hour Benefits: Medical, Dental, Vision, 401K (provided minimum eligibility hours are met) Magnit has an ongoing commitment to the diversity and inclusion of all team members. We believe that embracing diversity leads to innovation and helps address the needs of the business. We welcome individuals from different backgrounds, experiences, and cultures to join our team. We value this diversity and strive to create an inclusive environment that celebrates these unique perspectives, allowing you to contribute to your full potential. Finally, but most importantly, we expect all team members to be treated with dignity and respect. Important: Genentech has mandated COVID-19 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.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null}, {"id": 137454583905, "name": "Scientist III", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1679611772, "t_create": 1679611555, "ats_job_id": 137454583905, "display_job_id": 137454583905, "type": "ATS", "id_locale": "137454583905-en", "job_description": "\u25cf A BS or MS degree in Analytical Chemistry, Biochemistry, Biological Sciences or a related scientific discipline with 4+ years industry experience in pharmaceutical or biotechnology drug development. \u25cf In-depth knowledge and demonstrated proficiency in HPLC and mass spectrometry with a proven track record of solving bioanalytical problems. \u25cf Expertise in bioanalysis of therapeutic peptides/proteins or proteomics is required, with specific hands-on experience using QTRAP 6500/7500 and/or Orbitrap MS technologies as a plus. \u25cf Knowledge in immunoaffinity capture, proteolytic digestion/inhibition, and peptide analysis is a plus. \u25cf Have experience or are interested in gaining experience working with primary immune cells and cancer cell lines is required (eg. techniques of immune cell isolation, cellular phenotyping, cell activation and differentiation and antigen processing) \u25cf Experience in LC-MS/MS qualitative and/or quantitative method development is required. \u25cf Data analysis experience using different proteomic software including Proteome Discoverer, PMI or PEAKs is desirable. \u25cf A motivated team player with strong communication and interpersonal skills is essential. This is the pay range that Magnit reasonably expects to pay for this position: $70/hour-$120.66/hour Benefits: Medical, Dental, Vision, 401K (provided minimum eligibility hours are met) Magnit has an ongoing commitment to the diversity and inclusion of all team members. We believe that embracing diversity leads to innovation and helps address the needs of the business. We welcome individuals from different backgrounds, experiences, and cultures to join our team. We value this diversity and strive to create an inclusive environment that celebrates these unique perspectives, allowing you to contribute to your full potential. Finally, but most importantly, we expect all team members to be treated with dignity and respect. Important: Genentech has mandated COVID-19 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.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null}, {"id": 137454583673, "name": "Research Associate II", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1679609872, "t_create": 1679605480, "ats_job_id": 137454583673, "display_job_id": 137454583673, "type": "ATS", "id_locale": "137454583673-en", "job_description": "Routinely conduct protein purification using GE (AKTA) and HPLC systems and an automated liquid handling workstations. Carry out protein characterization and bio-analytical analysis using established or newly developed protocols Analyze datasets generated by bio-analytical instrumentation and upload results to data storage systems Establish and troubleshoot methods related to lab automation, purification, characterization, and assay development as the need arises Interact with members within the group and across the department to co-ordinate sample transfer, and communicate the status of ongoing projects Report directly to the group manager and present results and workflow progress at group meetings on a regular basis Experience with protein purification using GE (AKTA) and HPLC systems Knowledge of different types of columns pertaining to affinity, IEX, and Size exclusion chromatography Good quantitative data analysis skills and ability to handle large datasets Good written/verbal communication skills including experience with Microsoft Word, Excel and PowerPoint The ideal candidate will be meticulous, highly organized, pay great attention to detail, deliver consistent results, and possess the ability to work in a highly collaborative environment while interacting with different groups within and outside of the department Operational knowledge of automated liquid handling systems (e.g. Tecan, Hamilton, Dynamic Devices) and their application in support of purification, screening, and functional characterization of proteins is preferred but not required Experience with bio-analytical or biophysical techniques for protein characterization, such as HPLC-SEC, Mass Spectrometry, microfluidic electrophoresis (Caliper) BS or MS in biochemistry, biophysics, or a related field with relevant industry experience. This is the pay range that Magnit reasonably expects to pay for this position: $37.00/hour-$51.91/hour Benefits: Medical, Dental, Vision, 401K (provided minimum eligibility hours are met) Magnit has an ongoing commitment to the diversity and inclusion of all team members. We believe that embracing diversity leads to innovation and helps address the needs of the business. We welcome individuals from different backgrounds, experiences, and cultures to join our team. We value this diversity and strive to create an inclusive environment that celebrates these unique perspectives, allowing you to contribute to your full potential. Finally, but most importantly, we expect all team members to be treated with dignity and respect. Important: Genentech has mandated COVID-19 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.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null}, {"id": 137454570700, "name": "Research Associate I", "location": "Dixon, CA", "locations": ["Dixon, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1679501826, "t_create": 1679501145, "ats_job_id": 137454570700, "display_job_id": 137454570700, "type": "ATS", "id_locale": "137454570700-en", "job_description": "The Molecular Biology department seeks a motivated laboratory researcher who will assist in the discovery of groundbreaking therapeutics by supporting the primary research of several hundred internal customers. The responsibilities include processing samples in the laboratory (both manually and via laboratory robotics), analyzing and performing quality control of genetic data, and helping to evaluate and implement new technologies. Applicants should have a learning mindset, be able to work in a fluid and diverse environment and possess a strong desire to participate in research support efforts while feeling comfortable working primarily in a laboratory setting. Basic understanding of PCR, quantitative/real-time PCR (TaqMan; 5' nuclease assay), and other nucleic acid amplification and detection techniques. You should demonstrate the ability to create basic PCR and qPCR assays. High attention to detail Communicate effectively A more qualified candidate would also have functional knowledge regarding routine mammalian genetic constructs used in genome engineering, such as conditional knock-out models employing the Cre-Lox system. Bachelor's degree preferably in Life Sciences or engineering, with one to two years' job experience in an academic or industrial research laboratory (university and class experience does not qualify)", "stars": 0.0, "medallionProgram": null, "location_flexibility": null}, {"id": 137454540494, "name": "Scientific Researcher, Investigative Toxicology", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1678923363, "t_create": 1678922931, "ats_job_id": 137454540494, "display_job_id": 137454540494, "type": "ATS", "id_locale": "137454540494-en", "job_description": "Candidate will provide scientific and technical support to assays and platforms supported by the Investigative Toxicology group by performing experiments involving: immortalized and primary cell culture, cell viability assessment, ELISAs, gene expression analysis, high content screening, confocal microscopy, and flow cytometry. Experience with these methodologies is desirable, but not required. Maintaining documentation related to protocol execution and results. Writing protocols and contributing to final reports as appropriate. Adhering to departmental SOPs to ensure study integrity and quality. Conducting experiments with a high level of independence and initiative. Performing tasks with minimal direct supervision for routine methods and studies commonly employed by the team. Bachelors (BS/BA) in pharmacology, pharmaceutical science, biology, bioengineering, chemistry, physiology, or related discipline is required; Masters (MS) degree is desirable, but not required. 1-3+ years of laboratory experience with hypothesis-driven research. Ability to analyze, integrate, and present data in a presentation is required. Experience with immortalized and/or primary cell culture, cell viability assessment, ELISAs, gene expression analysis, high content screening, confocal microscopy, and flow cytometry is highly desired. Experience with complex in-vitro model systems is highly desired.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null}, {"id": 137454536513, "name": "Employee Communications Specialist", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1678902074, "t_create": 1678898634, "ats_job_id": 137454536513, "display_job_id": 137454536513, "type": "ATS", "id_locale": "137454536513-en", "job_description": "\u25cf Lead efforts to create our Q2 DevSci Town Hall presentation with leadership \u25cf Writes, edits, reviews and oversees release of internal communication documents and programs that support the organization \u25cf DevSci Senior Vice President communications support; including ad-hoc DevSci Leadership Team communication support \u25cf Maintain and update departmental intranet \u25cf Collect relevant information and stories for leadership monthly email updates \u25cf Support any updates or changes to existing DevSci Google sites \u25cf Communication/Slide support for DevSci Directors Meeting presentations (leadership business updates) \u25cf DevSci Community & Culture Team communication support (email creation, flyers, digital posters, ect) \u25cf Ad-hoc DevSci / TM communication support as needed \u25cf Excellent written and oral communication skills \u25cf Self-motivated, well organized and flexible \u25cf Works independently within guidelines and policies. \u25cf Creative problem solver and team player \u25cf Proficiency with Google Suite, Microsoft Office, and google sites \u25cf Experience with Adobe Illustrator, Video Editing software, and other design software is a plus This is the pay range that Magnit reasonably expects to pay for this position: $42.85/hour-$57.14/hour", "stars": 0.0, "medallionProgram": null, "location_flexibility": null}, {"id": 137454521762, "name": "Project Manager III", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1678736629, "t_create": 1678735274, "ats_job_id": 137454521762, "display_job_id": 137454521762, "type": "ATS", "id_locale": "137454521762-en", "job_description": "Manages project team information to support project team, LCT and/or LCC decision making Accountable for quality implementation on projects in the following areas: Project risk management; Critical path analysis; Scenario creation and analysis; Budget; Robust planning Ability to identify and communicate issues proactively to a wide range of stakeholders Creates, coordinates and maintains integrated project plans in Project & Portfolio Mgmt. Tool (PPM) Identifies gaps, potential bottlenecks or delays, challenges assumptions and proposes options to close gaps and get projects back on schedule Guides and manages preparation for project milestone reviews Manages meetings to include setting agendas, organizing meeting time and meeting minutes Consistently executes project management processes, and may lead improvement initiatives Follows best practices in project teams and fosters continuous improvement by sharing knowledge and continuous exchange * Performs other duties as assigned Problem solving skills and ability to coordinate project related activities Proficient in MS Project and/or Project & Portfolio Management Tool Ability to manage projects with ambitious milestones Ability to escalate and drive management decisions in relation to project execution and resource needs Understanding of relevant Design Control and/or Phased Development processes preferred This is the pay range that Magnit reasonably expects to pay for this position: $41.00/hour-$55.00/hour", "stars": 0.0, "medallionProgram": null, "location_flexibility": null}, {"id": 137454500794, "name": "Associate Quality Partner", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1678480641, "t_create": 1678480527, "ats_job_id": 137454500794, "display_job_id": 137454500794, "type": "ATS", "id_locale": "137454500794-en", "job_description": "Responsible for performing activities as required to meet Operations Quality goals and objectives with direction as appropriate. Performs assignments within existing procedures and instructions. Work day to day with limited supervision to correctly complete daily scheduled and unscheduled activities. Participate and implement process improvements to meet business needs. Build and maintain strong partnerships with colleagues and business patterns to assure alignment around strategic projects and day-to-day activities and to assure mutually successful working relationships. Build a culture of continuous improvement. Enable the organization's New Ways of Working: Review and evaluate Quality Data, visual inspection of finished goods, and Device History Records (DHRs) to ensure accuracy, completeness, appropriate release and control of products. Understand the requirements of the Quality System such as Good Documentation Practices, Quality Systems Procedures, Work Instructions, and Quality Records. Supports Verification activities, Audits, Training, Design Transfers, Validations, Non-Conforming Product, CAPA, Production & Process Controls, Storage & Handling, and Document & Data Control. Compiles and maintains daily Quality Assurance metrics to ensure compliance with quality system requirements and continuously promotes \u201cRight First Time\u201d Participate in continuous improvement initiatives and manufacturing projects Bachelor's / Master degree in Life Science, Data Science or related subject or equivalent experience. Completed training as a technician or laboratory technician; or equivalent qualification for the tasks; limited working experience..", "stars": 0.0, "medallionProgram": null, "location_flexibility": null}, {"id": 137454493387, "name": "Sr Software Engineer", "location": "Santa Clara, CA", "locations": ["Santa Clara, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1678374955, "t_create": 1678374612, "ats_job_id": 137454493387, "display_job_id": 137454493387, "type": "ATS", "id_locale": "137454493387-en", "job_description": "Design conception, design reviews for components or features, development, and testing of the core software stack. Builds, maintains, and extends our DevOps toolset to ensure ongoing improvements to team productivity and product scalability; lead team members to design, plan, deliver and operate high-quality software Ability to understand complex workflows and develop and validate innovative solutions to solve difficult problems Experience in API Design, Data Modeling, Capacity planning Experience architecting and developing large scale design Experience in Agile methods for both delivery and operations Experience of on-call production support, lead incident resolution Master in CS, Engineering (Preferred) Experience in Healthcare tech, standards, and workflows (e.g. HL7, FHIR) Experience with QMS for FDA-regulated products Experience in Data Analytics, Machine Learning", "stars": 0.0, "medallionProgram": null, "location_flexibility": null}], "debug": {}, "count": 72, "location_user": "any", "location_used": "", "locationInsights": null, "showWizard": 1, "disableLocationSearchDropdown": false, 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