{"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": "<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 Magnit Global & eightfold.ai</a> </p>", "page-footer-text": "powered By"}, "hideJobCart": false, "recaptcha_enabled": 0}, "positions": [{"id": 137453682888, "name": "Research Associate IV", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1670457886, "t_create": 1670457706, "ats_job_id": 137453682888, "display_job_id": 137453682888, "type": "ATS", "job_description": "To independently design, implement and report in vitro and in vivo studies. To make independent and innovative intellectual contributions to advance the program. To interact and communicate with other groups as part of a diverse multidisciplinary team. The successful applicants will have a PhD in immunology, molecular biology, biochemistry or related field. Candidates must be familiar with immunological principles and techniques including primary cell isolation, cell culture and flow cytometry. A strong background in myeloid cell immunology, molecular biology, and innate sensing of nucleic acids is highly desired. Excellent oral/written communication skills and creative problem-solving will be expected.", "stars": 0.0, "medallionProgram": null, "id_locale": "137453682888-en"}, {"id": 137453682872, "name": "Data Architect", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1670456324, "t_create": 1670456176, "ats_job_id": 137453682872, "display_job_id": 137453682872, "type": "ATS", "job_description": "Analyze data and data architecture to simplify processes including integration, transfer and extraction. Defines how the components of all the applications relate to each other, and how to best support the capability or the business area. Ensures the application components align with the application architecture and meet application performance goals. Performs technology due diligence on software development and architecture topics, including locally developed and open source. Helps to drive cross functional technical alignment on the definition, understanding & architecture of technologies and solutions in several key areas, to include cross capability, cross release issues, and issues affecting application integrity. Works with cross-functional teams to architect innovative operating alternatives that form the overall operating strategy and business architecture. Analyzes the impact of process or technical tool changes on existing processes, tools, and interfaces based on knowledge of interdependence of related functions and systems Ensures adequacy and quality of process controls and procedure documentation. Excellent communication and relationship skills, especially the ability to articulate advanced technical topics to non-technical individuals. Ability to contribute to multiple projects/demands simultaneously. Entrepreneurial drive with demonstrated ability to achieve/stretch goals in an innovative and fast paced environment with shifting priorities and loosely defined objectives. Ability to operate successfully in an unstructured, fluid environment - comfortable \u2018taking a position' with imperfect or incomplete information. Ability to constantly build, leverage and influence large network of senior technology and business experts across a large, diverse enterprise, and outside: standards bodies, analysts, and academia. Ability to demonstrate initiative, tenacity and persuasive capabilities to identify, form and drive forward new projects with limited formal process or managerial oversight. Ability to provide expertise and thought leadership on diverse modern software development practices and trends, across multiple platforms (desktop, mobile, data center, cloud), languages, databases etc. Excellent long term technological capability and operating cost optimization. Adept at influencing change/improvement in the organization beyond their own team. Information Security and Data Privacy fundamentals This is the pay range that Magnit reasonably expects to pay for this position: $56.00/hour-$65.00/hour", "stars": 0.0, "medallionProgram": null, "id_locale": "137453682872-en"}, {"id": 137453626488, "name": "Sr. Project Controls Engineer", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1669999353, "t_create": 1669999250, "ats_job_id": 137453626488, "display_job_id": 137453626488, "type": "ATS", "job_description": "Ensures that the Project Controls Processes are carried out in accordance with the Design & Construction Engineering Manual and the specific project-related Project Controls Plan. Coordinates, leads/supervises and monitors the Project Controls activities of Contractors and other involved parties. Manage the interface for Project Controls activities to all required Genentech Departments involved in the project (e.g. Finance, Procurement). Implements project controls procedures and systems, project controls training and workshops for project management team and/ or contractor. Reviews GC GMP bids as a member of the bid review team. Establishes and maintains WBS (Work breakdown Structure) and project cost ledger. Implements cost control, total project forecasting, and monthly cash-flow forecast based on the analysis of the actual incurred cost against the agreed budget, inclusive of work in place and project trends. Monitor cost performance to detect and understand variances from the budget. Produce accurate and unbiased cost forecasts at a detailed and summary level. Identify and ensure early warning of adverse cost trends such that corrective actions may be taken. Manage, review, and approve the project change requests (PCN Process). Incorporates the changes to the scope, schedule and cost into reporting. Leads/facilities risk workshops and manage the risk log and mitigation plans. Provides input to the project reports including Project Monthly Reports and is accountable for cost and schedule data in Cora PPM. Assist in the implementation of project financial accounting procedures and systems. Skills and abilities: Proficient in using MS-Office and/or Google Suite applications. Very good data analytical skills and advanced Excel skills. Ability to troubleshoot and work independently as well as within a team. Knowledge of SAP finance module. Experience utilizing a CAPEX Project Portfolio Management system to manage CAPEX projects. (eg Unifier, Ecosys, Ebuilder, Cora). Education: University degree in engineering or economics/business administration or equivalent (e.g. cost engineer, quantity surveyor) Minimum 10 years of experience in the area of project management and project controls.", "stars": 0.0, "medallionProgram": null, "id_locale": "137453626488-en"}, {"id": 137453414490, "name": "Research Associate III", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1669650675, "t_create": 1669650608, "ats_job_id": 137453414490, "display_job_id": 137453414490, "type": "ATS", "job_description": "Provide viral vector core services, which include lentiviral library production, Adeno-associated virus (AAV) production and viral vector analytics. Maintain virus inventory and registry using informatics platform such as the Benchling system. Assist with viral vector technology development and application for in vitro or in vivo genome engineering. Work independently within a dynamic, highly collaborative research environment. Proficient in mammalian cell culture and general molecular biology techniques such as transient plasmid transfection, PCR, qPCR, ddPCR and Western blot. Working experiences with lentivirus or AAV production and application, CRISPR technology for genome editing are highly desirable. Experiences with flow cytometer operations and electronic notebook are also a plus. Must be self-motivated, detail-oriented, analytical, highly organized, and have excellent communication and interpersonal skills. MS/PhD degree in Cell Biology, Molecular Biology, Virology, Biochemistry, Genetics, or a related discipline with 3+ years of laboratory research experience.", "stars": 0.0, "medallionProgram": null, "id_locale": "137453414490-en"}, {"id": 137453356119, "name": "System Engineer II/III", "location": "Pleasanton, CA", "locations": ["Pleasanton, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1668780000, "t_create": 1668779349, "ats_job_id": 137453356119, "display_job_id": 137453356119, "type": "ATS", "job_description": "Develops and deploys a wide range of technologies, including sample extraction, library preparation, sequencing, and analysis. Performs integration testing of system components and assesses performance against system-level product requirements. Participates in managing the total product development lifecycle spanning from product concept to launch. Creates and maintains design artifacts in Design History Files. Organizes, writes, and executes test cases for requirement verification. Ensures complete and comprehensive coverage of requirements in the test campaign. Develops and manages system-level product requirements and traceability analysis. Performs product risk management activities using tools such as Hazard Analysis or Failure Modes and Effects Analysis (FMEA). Updates work progress in collaboration tools (Jira, Confluence, Kanban, Slack) Keeps supervisor/project leader informed of project status, particularly of significant findings and results in critical problem areas. Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g. OSHA) Assesses results for applicability, validity, and conformance to Product Requirements Works independently with general management direction to drive product development and collaborates to identify opportunities for continuous process improvement. Maintains compliance as required by regulatory bodies and the company's quality system. Work closely with internal stakeholders to understand and resolve product performance issues. Level II Bachelor's degree in Chemistry, Biology, Biomedical Engineering, System engineering or related disciplines. Advanced degree preferred. Required BS or equivalent with 2-3 years related experience Hands-on experience with next generation sequencing platforms and/or robotic liquid handlers Experience working with IVD medical device systems. Experience integrating components into a system. Experience in product risk management, integration and verification testing, and requirements management", "stars": 0.0, "medallionProgram": null, "id_locale": "137453356119-en"}, {"id": 137453348114, "name": "Research Associate, Complex in-vitro Systems", "location": "South San Francisco, Ca", "locations": ["South San Francisco, Ca"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1668650843, "t_create": 1668650699, "ats_job_id": 137453348114, "display_job_id": 137453348114, "type": "ATS", "job_description": "Bachelor's (BS/BA) degree in bioengineering, chemical engineering, biology, physiology, pharmaceutical sciences or related discipline is required. A Master's degree (MS) is not required but preferred. Candidate will provide technical support to assays and platforms supported by the CiS group by performing duties that may include the following. Experience with all of the listed activities is not required. Routine culture and maintenance of immortalized, stem, and primary cell cultures, both in standard formats (flask or well plate) as well as organoids or organ-on-chip formats. Experience with these systems, and experience with a variety of different cell types (e.g. endothelial cells, GI stem cells, lung cells, etc) is highly desirable. Routine quantitative endpoint assays, such as immunostaining, confocal imaging and image analysis, high content imaging, qPCR, Luminex, ELISA, cell viability assays, etc. Performing tasks required for laboratory upkeep, such as: routine sterilization of incubators, routine mycoplasma testing, restocking of general laboratory supplies, etc. The candidate must have strong hypothesis driven research skills, problem-solving skills, and strong verbal and written communication skills. Especially critical for this role is organizational skills: the candidate will be asked to contribute on multiple different projects simultaneously, and proper organization of relevant protocols, observations, and data is key. Experience with high throughput or automated systems is a plus but not required. Need for excellent collaborative skills across the team and with key stakeholders Ability to analyze, integrate, and present data to collaborators and stakeholders and outside meetings as appropriate Maintaining electronic documentation related to departmental SOP adherence, execution, and results, and contributing to final reports as appropriate. Conducting experiments with a high level of independence and initiative, and performing tasks with minimal direct supervision for routine methods. 1-3+ years minimum of laboratory experience with hypothesis-driven research; we will also consider candidates with more years of experience. Ability to analyze, integrate, and present data in a presentation is required. Experience with immortalized and/or primary cell culture is required. Experience with organoid, organ-on-chip, or other MPS culture platform is highly desired. Experience with quantitative end point assays (e.g. confocal microscopy, qPCR, Luminex, Cell-Titer) is highly desired.", "stars": 0.0, "medallionProgram": null, "id_locale": "137453348114-en"}, {"id": 137453348095, "name": "Research Associate II / III \u2013 Assay Transfer", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1668650241, "t_create": 1668650034, "ats_job_id": 137453348095, "display_job_id": 137453348095, "type": "ATS", "job_description": "Responsible for transitioning products from Development to Manufacturing as a member of the Assay Transfer team. Prepares manufacturing documents and completes transfer activities for new products, including pilot lot formulation. Executes laboratory research as it pertains to process characterizations or other manufacturing matters. Investigates development and manufacturing process strategies to support new and existing reagent products. Executes research and development activities for products, methods and/or processes to ensure manufacturability. Prepares manufacturing documents, technical reports, summaries and quantitative analyses. Manufactures GMP lots and participates in process characterizations for reagents transferring to Manufacturing. Collaborates with other functions regarding Design Transfer activities. Maintains complete and accurate records. Normally receives general directions on routine work and detailed instructions on new work by more experienced members of the Assay Transfer team. Makes suggestions to improve work processes. Works on projects of diverse scope in which analysis of situation or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. May participate in project team meetings and other cross functional collaboration. Presents and discusses data within group. Monitors work to ensure quality, and continuously promote Quality First Time. Knows basic and some specialized laboratory techniques. Familiar with manufacturing processes and/or design transfer activities. Familiar with searching scientific literature. Skilled with use of word processing, spreadsheets, graphical and presentation software applications. Hourly Pay Rate Range (dependent on location, experience, expectation): $27-34/hr 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, "id_locale": "137453348095-en"}, {"id": 137453347080, "name": "Automation Engineer V", "location": "Oceanside, Ca", "locations": ["Oceanside, Ca"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1668649692, "t_create": 1668643774, "ats_job_id": 137453347080, "display_job_id": 137453347080, "type": "ATS", "job_description": "Perform automation and instrumentation and control engineering design services for existing facility projects, including upgrades and capacity expansions, equipment upgrading and replacement. Produce and review design drawings and specification documents (URS, FS, DS, etc.). Generate, execute, and review design testing, generate and participate in functional specification testing, and perform field inspection services. Generate, execute, and review Installation, Operational, and Performance Qualification protocols. Generate, review, and approve GMP Lifecycle Documents (e.g. risk documents, trace matrices, periodic review, etc.) Execute and track progress of change records. Troubleshooting of automation and critical process utility systems. Lead plant operations to assess discrepant events and changes for automation impact, deliver automation solutions to resolve operational issues, assist in troubleshooting and providing real time on floor support of manufacturing operations, participate in site coordination meetings and attend network meetings. Adhere to site SOPs and WIs for daily and project deliverables and provide improvements to business processes. Attendance and participation in department and staff meetings. Maintain training qualifications. Adhere to company policies regarding performance management, department time reporting and notification requirements, budget, and expense reporting guidelines. Track project deliverables, and provide status updates to project team. All employees with jobs that require access to the Warehouse must be able to pass the Transportation Security Administration (TSA) Security Threat Assessment (STA). Ensures the integration of environmental health, safety, and security into the business processes, systems, and programs while reporting safety and environmental incidents including injuries, illnesses, and safety suggestions within one's functional area. Fosters a positive safety culture in which no one gets hurt. Experience with Biopharmaceutical manufacturing, design or/and construction. Knowledge of process, utility and building control systems. Knowledge of GMP guidelines, experience in generation of controlled documents. Qualification experience related to control and computer systems. Ability to generate engineering drawings and specifications. Knowledge of ISA standards and practices for instrumentation. Knowledge of PID control theories and techniques. Knowledge of programmable logic controllers, and associated programming languages (RS Logix Preferred). Practical knowledge of distributed control systems, and associated programming languages - ***Strong DeltaV Coding P2 experience is strongly preferred. Knowledge of computer aided manufacturing automation. Demonstrate good organizational and time utilization skills. Demonstrate good written and verbal communication skills. Ability to comply with cGMP requirements (gowning, documentation, and procedures) for performing work within the manufacturing facility. Demonstrate strong working knowledge of PC based programs and web based systems. Ability to work most of the time independently with minimal direct supervision. Demonstrate good interpersonal skills with an ability to interact well with a variety of personalities, discipline skills and educational levels. Bachelor's or Master's degree in Engineering (Chemical, Mechanical, Electrical, or Computer Science preferred) and 5 years' experience, or Master's degree in Engineering (Chemical, Mechanical, Electrical, or Computer Science preferred) and 4 years' experience. Minimum of 8 years applicable automation and/or instrument and control system experience. Minimum of 5 years in the pharmaceutical/biotech industry/GMP experience.", "stars": 0.0, "medallionProgram": null, "id_locale": "137453347080-en"}, {"id": 137453346901, "name": "Clinical Imaging Analyst", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1668643321, "t_create": 1668642471, "ats_job_id": 137453346901, "display_job_id": 137453346901, "type": "ATS", "job_description": "Your responsibilities will include working with a diverse team of scientists and IT staff to curate, organize, and document clinical images and associated clinical data from clinical trials. Work with scientists, contractors, and IT staff to curate, organize, and document clinical images and associated clinical data from clinical trials Support data integration efforts across diverse data sources Support annotation pipelines using the image data Support development of Machine Learning/Deep Learning (ML/DL) algorithms and pipelines using the image data Continually search for opportunities to automate workflows and streamline processes Master's or PhD in Computer Science, Biomedical Engineering, or a similar discipline Experience with clinical imaging in Ophthalmology and/or Respiratory (e.g., OCT, CT, MRI, etc.) Experience with medical/clinical image data analysis techniques Proficient in scripting languages such as Python, Matlab, etc. Experience with ML/DL, proficient with DL frameworks like PyTorch, TensorFlow, etc. Familiarity with medical image formats (e.g., DICOM, NIfTI) Some experience with database applications Understanding of clinical trials a plus Excellent communication and presentation skills Proactive attitude", "stars": 0.0, "medallionProgram": null, "id_locale": "137453346901-en"}, {"id": 137453342894, "name": "Senior Research Associate / Scientist \u2013 Investigation and Resolution", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1668631160, "t_create": 1668631146, "ats_job_id": 137453342894, "display_job_id": 137453342894, "type": "ATS", "job_description": "\u25cf Conducts independent reagent-based or assay-based investigations and resolution projects in alignment with business and compliance needs \u25cf Contributes to the technical execution and timeliness of CAPAs/NCRs and on-market support (OMS) \u25cf Designs experimental plan to support project objectives \u25cf Executes bench experiments; makes detailed and general observations and analyzes data \u25cf Prepares technical reports, summaries and quantitative analyses \u25cf Maintains complete and accurate records \u25cf Normally acts independently for developing methods, techniques and evaluation criteria for obtaining results \u25cf Identifies and implements improvements to work processes and laboratory environment \u25cf Recognized expert across a wide range of techniques and their application \u25cf Works on extremely complex problems in which analysis of situations or data requires an evaluation of intangible variables \u25cf Exercises independent judgment in developing methods, techniques and evaluation criteria for obtaining results \u25cf Participates or leads cross functional technical teams such as a failure investigation or core team \u25cf Works well in a team environment by being a productive project team member, suggesting creative solutions to problems and providing input to project planning \u25cf Establishes interfaces across other organizational groups \u25cf Conducts independent reagent-based or assay-based investigations and resolution projects in alignment with business and compliance needs \u25cf Contributes to the technical execution and timeliness of CAPAs/NCRs and on-market support (OMS) \u25cf Designs experimental plan to support project objectives \u25cf Executes bench experiments; makes detailed and general observations and analyzes data \u25cf Prepares technical reports, summaries and quantitative analyses \u25cf Maintains complete and accurate records \u25cf Normally acts independently for developing methods, techniques and evaluation criteria for obtaining results \u25cf Identifies and implements improvements to work processes and laboratory environment \u25cf Recognized expert across a wide range of techniques and their application \u25cf Works on extremely complex problems in which analysis of situations or data requires an evaluation of intangible variables \u25cf Exercises independent judgment in developing methods, techniques and evaluation criteria for obtaining results \u25cf Participates or leads cross functional technical teams such as a failure investigation or core team \u25cf Works well in a team environment by being a productive project team member, suggesting creative solutions to problems and providing input to project planning \u25cf Establishes interfaces across other organizational groups \u25cf Troubleshoots problems and institutes corrective action \u25cf Prepares and presents experimental procedures and results in group and project teams \u25cf Monitors work to ensure quality, and continuously promote Quality First Time \u25cf MS in Biology/Chemistry/Biochemisty or related field with ~1 year or more experience (Preferred) \u25cf BS in Biology/Chemistry/Biochemistry or related field with 6 yrs or more demonstrating progressive work experience of increased competencies \u25cf Demonstrated record of accomplishments within a FDA/IVDR regulated environment \u25cf Knows wide range of experimental techniques and skilled in their applications \u25cf Acts independently to determine methods and procedures on new assignments \u25cf Capable with searching scientific literature to gain general and specific information \u25cf Skilled with use of word processing, spreadsheets, graphical and presentation \u25cf Maintains broad knowledge of state-of-the-art principles and theories in chemistry, biochemistry and biology \u25cf Excellent time management, planning, organization and problem solving skills \u25cf Ability to work independently and as part of an interdisciplinary team to achieve project goals and timelines is required Ability to prepare and present information to groups \u25cf Uses professional concepts to contribute to the development of company concepts and principles and to achieve objectives in creative and effective ways \u25cf Experience with SAFe Agile methodologies is a plus Scientist: \u25cf Troubleshoots problems and institutes corrective action \u25cf Prepares and presents experimental procedures and results in group and project teams \u25cf Monitors work to ensure quality, and continuously promote Quality First Time \u25cf BS in Biology/Chemistry/Biochemistry or related field with 8 yrs or more demonstrating progressive work experience of increased competencies \u25cf MS in Biology/Chemistry/Biochemistry or related field with 3 yrs or more experience \u25cf Demonstrated record of accomplishments within a FDA/IVDR regulated environment \u25cf Knows wide range of experimental techniques and skilled in their applications \u25cf Acts independently to determine methods and procedures on new assignments \u25cf Capable with searching scientific literature to gain general and specific information \u25cf Skilled with use of word processing, spreadsheets, graphical and presentation \u25cf Maintains broad knowledge of state-of-the-art principles and theories in chemistry, biochemistry and biology \u25cf Excellent time management, planning, organization and problem solving skills \u25cf Ability to work independently and as part of an interdisciplinary team to achieve project goals and timelines is required Ability to prepare and present information to groups \u25cf Uses professional concepts to contribute to the development of company concepts and principles and to achieve objectives in creative and effective ways \u25cf Experience with SAFe Agile methodologies is a plus Hourly Pay Rate Range (dependent on location, experience, expectation): $34-42/hr 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, "id_locale": "137453342894-en"}], "debug": {}, "count": 250, "location_user": "any", "location_used": "", "locationInsights": null, "showWizard": 1, "disableLocationSearchDropdown": false, "pcsAutocompleteLocationEnabled": 0, "recommended_star_threshold": 4, "mocTitle": null, "query": 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