Contractor Positions for Roche and Genentech

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Evaluate changes in study protocols to determine the impact on clinical trial site budgets; develop, negotiate and finalize budget amendments. Provide continuing support on executed agreements (e.g., drafting amendments, extensions and terminations, interpreting contractual language in response to issues or questions that arise). Work closely and communicate with members of the Lifecycle Finance teams and other internal stakeholders; provide timely updates on contract and site budget status', identifying and escalating any potential critical path items as appropriate. Track, maintain and update assigned contract information within the COBM Clinical Trial Management System (CTMS) and other tracking tools, to ensure completeness and accuracy, as applicable. Works with Supplier Relationship Manager and Legal to establish Master Services Agreement (MSA) for as many suppliers as possible. Works with Supplier Relationship Manager to incorporate Key Performance Indicators into contracts for applicable suppliers. Establish Purchase Orders (PO), review related Invoices, track spend against contracts / PO's, and report spend as necessary. Other tasks may be assigned from time to time to support overall COBM function. Clinical Trials Contracting: MSA and contracts Vendor Management This is the pay range that Magnit reasonably expects to pay for this position: $32.00/hour-$46.39/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.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 137455398820, "name": "Project Scheduling Engineer", "location": "Oceanside, Ca", "locations": ["Oceanside, Ca"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1685740024, "t_create": 1685739871, "ats_job_id": 137455398820, "display_job_id": 137455398820, "type": "ATS", "id_locale": "137455398820-en", "job_description": "- Extensive experience planning and scheduling on complex Good Manufacturing Practice (GMP) biotech projects. - Facilitates understanding and alignment across multi-disciplinary groups and partners on a complex project. - Extensive knowledge Commissioning, Qualification, Validation, and Automation are integrated in a GMP Biotech project. - Ability to prioritize competing demands and manage multiple stakeholder requests. - Collaborate with project team to establish Project WBS and Work Packages - Participate in RFP preparation and bid reviews to ensure contractors' and vendors' schedule performance capabilities - Support contractors and vendors in developing discipline schedules to meet Project goals - Review various discipline schedules for its technical integrity, soundness of the contents and logic, and accuracy of updates - Facilitate pull planning sessions and support the implementation of Last Planner\u00ae System and Lean Construction - Assist Project's strategic planning and perform \u201cwhat-if\u201d analyses as needed - Apply change management process, evaluate the need for rebaseline and perform it as needed - Cost- and resource-load schedules as needed and assist resource planning - Perform or assist Risk Workshops and risk review sessions, and perform Monte Carlo simulations as required, interpret the results for the project team - Monitor project progresses, update Project Master Schedule and other relevant project schedules, report out and communicate the status - Analyze schedule performances (use Earned Value method as appropriate) to detect and understand variances from the Baseline, identify early warning of schedule trends, provide schedule forecasting, and assist project team in taking corrective actions - Perform schedule analysis such as critical path analysis, float trend analysis, variances analysis, multiple float paths analysis, etc. and provide the team with recommendations - Perform job progress walks periodically and check schedule updates accuracy - Provide input to the Project Monthly Reports and the Project Data Collection Report - Bachelor or University degree in engineering / economics / business administration - PMI or ACCEi Project Control Professional qualification or equivalent - Min 5 years work experience as project schedule engineer - Project Management and Project Controls - Experience in Biotech or Pharmaceutical CAPEX projects is preferred - Knowledge and experience in the Last Planner\u00ae System and Lean Construction is preferred - Proficiency in Primavera P6, MS Project, Monte Carlo Simulation software such as Pertmaster or Safran Risk, MS Office, Google Suite - Knowledge and experience in Earned Value Management This is the pay range that Magnit reasonably expects to pay for this position: $80.00/hour-$110.71/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, "work_location_option": null}, {"id": 137455379078, "name": "Associate Quality Partner", "location": "Pleasanton, Ca", "locations": ["Pleasanton, Ca"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1685588739, "t_create": 1685588630, "ats_job_id": 137455379078, "display_job_id": 137455379078, "type": "ATS", "id_locale": "137455379078-en", "job_description": "Attention to detail communication quality minded 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.. 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. 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.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 137455377150, "name": "Project Manager II", "location": "Tucson, Az", "locations": ["Tucson, Az"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1685570997, "t_create": 1685570680, "ats_job_id": 137455377150, "display_job_id": 137455377150, "type": "ATS", "id_locale": "137455377150-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 Manages preparation for project milestone reviews Manages meetings to include setting agendas, organizing meeting time and meeting minutes Executes project management processes 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 Strong written and oral communication skills Basic stakeholder management and facilitation skills 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", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 137455369757, "name": "DevOps Engineer", "location": "Tucson, Az", "locations": ["Tucson, Az", "remote"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1685553625, "t_create": 1685545563, "ats_job_id": 137455369757, "display_job_id": 137455369757, "type": "ATS", "id_locale": "137455369757-en", "job_description": "Implements strategies regarding the build environment, build artifacts, repository structure, branching and merging in supporting software development releases. Configures and improves the build process in coordination with the development team to resolve merge conflicts in support of CI/CD. Creates deployment packages according to the requirements for distribution, archiving, automated integration testing, and dependency handling. Creates Microsoft Azure DevOps (ADO) Team Projects, boards, dashboards, sprints, area/iteration paths, and manages permissions. Maintains quality gates, test automation, and analysis tools of the CI/CD pipeline for tracking and measuring software quality metrics across projects. Communicates status and/or results of build and repository related quality gates to include repository structure quality, build output structure quality, source code analysis results, code coverage and test results. Creates documentation according to applicable processes in the area of configuration, build, and release management. Proven knowledge of the end-to-end software development process, application infrastructure, and DevOps toolchain Ability to maintain DevOps project lifecycles and software source control tools in Microsoft Azure DevOps (ADO) environment. Expertise with Microsoft Azure DevOps (ADO) Process Templates, Work Item Types, and Boards. DevOps experience with troubleshooting, structured logging, and documenting software build and deployment processes. Knowledge of MSBuild and YAML with understanding of build pipeline principles and practices for Continuous Integration. Ability to integrate source, third party components, data, and deployment dependencies of a software system to implement CI/CD. Knowledge of containerization and orchestration technologies such as Docker and Kubernetes. Familiarity working with Public Cloud providers such as AWS, Azure, or Google Cloud Platform. Knowledge of configuration management tools such as Terraform and Ansible. Experience with C#.NET and PowerShell. DevOps experience with Operating Systems and Networking with Windows and/or Linux. Bachelor's Degree in MIS, Computer Science or related field.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 137455366549, "name": "Clinical Lab Scientist", "location": "Tucson, Az", "locations": ["Tucson, Az"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1685485265, "t_create": 1685485229, "ats_job_id": 137455366549, "display_job_id": 137455366549, "type": "ATS", "id_locale": "137455366549-en", "job_description": "Responsible for performing high complexity laboratory testing on clinical specimens, interpreting and reporting results and complying with study protocols, Standard Operating Procedures, Test Instructions, and related CAP/CLIA Regulations and guidelines. Participates in scientific studies and activities supporting registrational and non-registrational clinical trials. Works under general supervision, to support aspects of clinical testing and sample processing, adhering to CAP/CLIA regulations and ISO 15189 guidelines. Performs high-complexity testing within the CDx CAP/CLIA Laboratory. Monitors performance of IHC, ISH, molecular assays, and immunoassays; assists with lab failure investigations and root cause analysis. Performs accessioning of biological samples (blood, plasma, tissue) and quality control of demographic data input. Communicates with clients on held and rejected samples. Performs work according to established internal safety guidelines and procedures, and as specified by appropriate regulatory agencies (SHE, OSHA) Critically evaluated quality control and test results against acceptance criteria to support clinical testing. Uses technical writing skills and Good Documentation Practices to complete lab documentation, SOPs, and Quality documents. Participate in routine lab maintenance and lab safety inspections. May perform basic troubleshooting for issues related to instrumentation. Analyzes alternative approaches to solve problems or develop new perspectives on existing solutions; initiate and implement process improvements. Other duties as assigned by management. To perform this job successfully, an individual must be able to perform each responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the responsibilities. Bachelor's Degree Immunohistochemistry (IHC), chromogenic in-situ hybridization (ISH), histology lab experience (CAP/CLIA), immunoassays and molecular biology experience. Demonstrated proficiency in computer skills, such as word processing, statistical analysis, and laboratory information systems. Excellent verbal and written communication skills. Strong understanding of good laboratory practices and regulatory compliance. Requires excellent attention to detail; ability to multi-task and be flexible with tasks and schedules.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 137455324997, "name": "System Engineer I", "location": "Pleasanton, Ca", "locations": ["Pleasanton, Ca"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1685416399, "t_create": 1685416062, "ats_job_id": 137455324997, "display_job_id": 137455324997, "type": "ATS", "id_locale": "137455324997-en", "job_description": "Carry out tasks as necessary to run test campaigns to verify requirements and design specifications. Collect, analyze, and develop report packages to support system verification and validations. Conduct material & system characterization Troubleshooting and data analysis of issues during development and in the field Excellent problem-solving skills and ability to work with minimal direction in an interdisciplinary environment. Exceptional people skills, strong communication, flexible personality, able to work independently and as part of a team. Strong skills in writing technical reports and verbally communicating technical content in oral presentations B.S. or M.S. in Engineering, Physical, and/or Biological Sciences, or related field.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 137455249000, "name": "Procurement Excellence and Operations Manager", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1684890416, "t_create": 1684890265, "ats_job_id": 137455249000, "display_job_id": 137455249000, "type": "ATS", "id_locale": "137455249000-en", "job_description": "\u25cf Successful Project Deployment and support: \u25cb Coordination of all the ASPIRE Procurement solutions deployment (SAP S4H for Direct Procurement, GEP Nexxe for supplier collaboration, and GEP Smart for Indirect procurement) \u25cb Align/Monitor with the 3rd party partner the deployment activities. \u25cb All milestones and deliverables according to the project plan are on time and within the expected quality \u25cb The promotion and the deployment of the Global Template solution and potential deviations are handled according to the defined processes with the relevant development team. \u25cb Together with the Business Process Management and/or other teams, lead the successful execution of process workshops and alignment sessions with the sites. \u25cb All go-no-go criteria are met and approved by the relevant customer. \u25cb Conduct change impact analysis. Implement practical and sustainable processes aligned with the new system. \u25cf Lead/ partner for analysis and management of Procurement Operational activities & Issue Resolution: \u25cb Analytical Problem Solving - Ability to identify problems, define problem statements clearly and accurately and apply structured and disciplined methodology to identify data-driven root causes. Innovative and effective in solution development, risk mitigation, and execution. \u25cb Identify & document potential process/system improvements. Ensure the system improvements are implemented or added to the system roadmap. \u25cb Execute/ lead/ partner on targeted operations activities that need to be completed to meet the project or are required per standard procurement operations (e.g. Clean/ update Master data, followup with Suppliers to drive a deployment/ change and other activities). \u25cf You're someone who wants to influence your own development. You're looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point. \u25cf You have an appropriate University degree in Business or Industrial Engineering, and 7+ years of project deployment, E2E Process Improvement related work experience, preferably in Procurement (direct) and other Procurement operational experience in Pharma/Biotech industry. Finance, Supply Chain & Direct Materials experience is a plus. \u25cf Lean Six Sigma Black Belt Certification is a preferred. \u25cb Excellent communication skills, with demonstrated proficiency in influencing, negotiating, and effective global collaboration. Ability to effectively communicate across various levels of a complex, matrix organization. \u25cb Service orientation mindset to shape a high-quality and reliable project delivery service. Experience in a Business Operations environment is a plus. \u25cb Proven track record of efficient stakeholder management \u25cb Demonstrated ability to successfully direct, coordinate, and strategically integrate multiple streams of information and activities at a program level. \u25cb You are a self-driven professional, adaptable and resilient, with a growth mindset. \u25cb Digital savvy and process efficiency-oriented person. \u25cb SAP S4H experience will also be appreciated. This is the pay range that Magnit reasonably expects to pay for this position: $64.07/hour-$85.43/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, "work_location_option": null}, {"id": 137455227474, "name": "Systems Support Engineer I", "location": "Santa Clara, CA", "locations": ["Santa Clara, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1684853814, "t_create": 1684799927, "ats_job_id": 137455227474, "display_job_id": 137455227474, "type": "ATS", "id_locale": "137455227474-en", "job_description": "1. Complete monthly third party preventive maintenance documentation, plans and executes assigned work. Needs to be present on-Site during core work hours, (generally 8:30am to 5pm) 2. All activities performed are documented accurately and in a timely manner in the electronic instrument database according to approved procedures, will triage and resolve tasks that are assigned via our Team Zone ticket system visible to internal lab customers 3. Attend daily meetings to update leads and group on assignments 4. Learn to analyze alternative approaches to creatively solve problems and/or develop new perspectives on existing solutions under general supervision 5. Provide effective and professional customer support at all times 6. Associates degree in electrical or electronic engineering or equivalent training with 0 - 1 years relevant work experience with basic knowledge of instrument support Demonstrated proficiency to learn new skills/software/tools rapidly Must be able to consistently follow instructions with a cooperative, \u201ccan do\u201d attitude Must be organized, in order to accommodate changing volume of work Ability to be flexible with changing work priorities Strong work ethic Bachelor's degree or equivalent in engineering or related field 1 + years in medical device industry, preferably \"hands on\" experience with medical instrument maintenance Basic understanding of molecular diagnostics products Working knowledge of hand tools and electronic test equipment Knowledge of Quality System Requirements (QSR), In Vitro Diagnostics Directive This is the pay range that Magnit reasonably expects to pay for this position: $34.00/hour-$43.00/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. 7. Comply with safety policies, practices and procedures at all times. Maintain safe work habits and practices with regard to safety requirements in-house 8. Work/align/collaborate with our Lab Supervision team on compliance and organization in the labs. This would include provision of space for instruments and utilities 9. Provide limited IT support to laboratory systems", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 137455177632, "name": "BioRepository Technician II/Sr. Biorepository Technician", "location": "Pleasanton, California", "locations": ["Pleasanton, California"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1684292602, "t_create": 1684292482, "ats_job_id": 137455177632, "display_job_id": 137455177632, "type": "ATS", "id_locale": "137455177632-en", "job_description": "The BioRepository Technician II/Sr. Biorepository Technician position will facilitate the daily operation associated with the Biorepository in the Biospecimen Acquisition and Management (BAM) function. Daily operation includes, but is not limited to, processing, distribution, storage, inventory management, and disposition of biological materials. Biological materials serve as the foundation for research, development and validation of diagnostics products. Availability of specimens is a critical and often a \u201crate limiting\u201d step in research, development, launch, and support of products. Careful management of the planning, procurement, inventory and distribution process is key to success. Performs Biorepository Management duties for Biospecimen Acquisition and Management (BAM) with meticulous attention to details. Works independently and provides training/oversight of junior associates to receive shipments of human biological samples, verify sample integrity and data accuracy, complete the sample check-in process in the validated Laboratory Information Management System (LIMS), consolidate inventory, retrieve and distribute samples, ship specimen collection supplies to partners, and monitor laboratory supply inventory. Works independently in the LIMS, maintaining documentation in accordance with established procedures; performs moderately complex database queries as needed. Maintains a high level of organization to independently manage all aspects of complex service requests at the program level and thinks creatively to resolve challenges as encountered. Participates in laboratory certification and accreditation management activities, audit preparation, and team member recruitment activities; maintains order and cleanliness of lab and controlled temperature units. Provides input to improve existing laboratory procedures. Assists in development and implementation of standard operating procedures. May support coordination of material testing services. Participates in required training related to position; takes personal responsibility for being current in all training activities. Manages daily activities/responsibilities and assignments to meet business needs; establishes priorities using inputs from business requirements and/or internal customer needs. BS Degree in Biological Science or related field, or equivalent combination of education and work experience. Minimum 3 years of relevant laboratory experience. Requires work with dry ice, -80 degree freezers, and human biological samples. Ability to lift objects up to 30 lbs. Ability to work in a fast paced and dynamic environment with efficiency; capable of handling multiple projects Passionate about the importance of biorepository management Proficient in using G(oogle)-Suite Ability to work independently and as a team member", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}], "debug": {}, "count": 48, "countFilterByMatchScore": null, "location_user": "any", "location_used": "", "locationInsights": null, "showWizard": 1, "disableLocationSearchDropdown": false, "pcsAutocompleteLocationEnabled": 0, "recommended_star_threshold": 4, "mocTitle": null, "query": {"query": "", "location": "", "department": [], "skill": [], "seniority": [], "pid": ""}, "userTitles": [], "isThinProfile": false, "veteranProgramDetails": [], "enableTargetedResume": 0, "jobCardConfig": null, "facets": {"skills": {"SAP": 6, "GMP": 5, "Project Management": 5, "Clinical Trials": 2, "Contract Research Organization": 2, "Data Analysis": 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