Computational technologies are increasingly a core part of drug discovery and development. We are on a mission to leverage big data, massive computing power, as well as advanced AI algorithms to provide far more therapies at far less cost to society. Genentech's Early Clinical Development (ECD) department is seeking an Artificial Intelligence Imaging Scientist/Engineer reporting to the head of AI and Cloud Engineering. The AI & Cloud Engineering (ACE) group breaks new ground in applying advanced AI methods including Deep Neural Network to medical imaging datasets to support clinical decisions, operational decisions, patient response and safety prediction, and personalized medicine clinical development. The AI Imaging scientist will primarily be responsible for the research and development and validation of deep learning methods in early research and early clinical development, which significantly contribute to the advancement of Genentech's drug development...
Jan 21, 2021
Computational technologies are increasingly a core part of drug discovery and development. We are on a mission to leverage big data, massive computing power, as well as advanced AI algorithms to provide far more therapies at far less cost to society. Genentech's Early Clinical Development (ECD) department is seeking an Artificial Intelligence Imaging Scientist/Engineer reporting to the head of AI and Cloud Engineering. The AI & Cloud Engineering (ACE) group breaks new ground in applying advanced AI methods including Deep Neural Network to medical imaging datasets to support clinical decisions, operational decisions, patient response and safety prediction, and personalized medicine clinical development. The AI Imaging scientist will primarily be responsible for the research and development and validation of deep learning methods in early research and early clinical development, which significantly contribute to the advancement of Genentech's drug development...
External Job Posting Position Overview: The Therapeutic Area Medical Science Liaison (TA MSL) is a credible scientific partner responsible for providing clinical and health economic information related to disease states and the appropriate utilization of Genentech medicines (approved and pipeline). This field-based position will engage with healthcare providers, population health decision makers, and patients within their region(s), to further patient outcomes aligned with the overarching objectives of Genentech. In collaboration with their regional partners, TA MSLs are accountable for co-creating the local medical strategy and delivering for their customers. In addition, TA MSLs may be responsible for covering multiple medicines, as well as engaging in broad scientific discussions around patient outcomes and total cost of care, resulting in rich customer insights shared with key stakeholders across the organization. Key Responsibilities/Accountabilities: Ensure an...
Jan 21, 2021
External Job Posting Position Overview: The Therapeutic Area Medical Science Liaison (TA MSL) is a credible scientific partner responsible for providing clinical and health economic information related to disease states and the appropriate utilization of Genentech medicines (approved and pipeline). This field-based position will engage with healthcare providers, population health decision makers, and patients within their region(s), to further patient outcomes aligned with the overarching objectives of Genentech. In collaboration with their regional partners, TA MSLs are accountable for co-creating the local medical strategy and delivering for their customers. In addition, TA MSLs may be responsible for covering multiple medicines, as well as engaging in broad scientific discussions around patient outcomes and total cost of care, resulting in rich customer insights shared with key stakeholders across the organization. Key Responsibilities/Accountabilities: Ensure an...
Global Product Strategy (GPS) sets and delivers strategic business direction from late stage research & development through to commercialization and medical excellence for the benefit of patients and our customers. Part of the Global Pharma Communications Team, the International Communications Leader (ICL) sits within The Centre of Excellence for Product and Portfolio. The ICL primarily helps to drive Roche Pharma product development & commercial objectives through high impact external communications strategies. The ICL plays a crucial role on the lifecycle team and as the principal communications lead for this group providing counsel to the Lifecycle Leader and the Integrated Strategy Leader. Given the nature of this position, the ICL works closely with various cross-functional partners and stakeholders, including Group Communications, Investor Relations, Genentech Corporate Relations, GPS & PD Therapeutic Area and Franchise leaders, Affiliate communicators, etc....
Jan 20, 2021
Global Product Strategy (GPS) sets and delivers strategic business direction from late stage research & development through to commercialization and medical excellence for the benefit of patients and our customers. Part of the Global Pharma Communications Team, the International Communications Leader (ICL) sits within The Centre of Excellence for Product and Portfolio. The ICL primarily helps to drive Roche Pharma product development & commercial objectives through high impact external communications strategies. The ICL plays a crucial role on the lifecycle team and as the principal communications lead for this group providing counsel to the Lifecycle Leader and the Integrated Strategy Leader. Given the nature of this position, the ICL works closely with various cross-functional partners and stakeholders, including Group Communications, Investor Relations, Genentech Corporate Relations, GPS & PD Therapeutic Area and Franchise leaders, Affiliate communicators, etc....
Instrumentation Technician Scope: The Instrumentation Technician is responsible for performing service activities relating to the calibration, maintenance and repair of laboratory calibration instruments/equipment. Responsibilities: Provide calibration, troubleshooting, and repair of analytical instruments used in laboratories. Installation, calibration, troubleshooting, and modification of analytical systems, laboratory instruments and analyzers. Enter calibration data and service information into the calibration management system. Respond to trouble calls and perform diagnostics and repairs. Timely completion of tasks and work orders with appropriate documentation according to Standard Operating Procedures, applicable standards, guidelines, practices, and policies. Escort vendors in need of lab access to perform assigned calibration and maintenance work. Ensure vendor provides complete maintenance documentation upon work completion. Review and process...
Jan 20, 2021
Instrumentation Technician Scope: The Instrumentation Technician is responsible for performing service activities relating to the calibration, maintenance and repair of laboratory calibration instruments/equipment. Responsibilities: Provide calibration, troubleshooting, and repair of analytical instruments used in laboratories. Installation, calibration, troubleshooting, and modification of analytical systems, laboratory instruments and analyzers. Enter calibration data and service information into the calibration management system. Respond to trouble calls and perform diagnostics and repairs. Timely completion of tasks and work orders with appropriate documentation according to Standard Operating Procedures, applicable standards, guidelines, practices, and policies. Escort vendors in need of lab access to perform assigned calibration and maintenance work. Ensure vendor provides complete maintenance documentation upon work completion. Review and process...
About EpiCX EpiCX, the Global Customer Engagement Program, is a business and IT transformation program, currently in flight and planned to be completed in 2023 across 100+ affiliates. Its main ambition is to add meaning and value to all Roche's customer interactions through a single, common, customer-centric technology ecosystem. The EpiCX program will develop and deploy an enterprise-wide ecosystem which integrates world-class orchestrated customer engagement, content management, data and analytics products into one harmonized, centralized and scalable technology ecosystem. This ecosystem will run across all Roche Pharma affiliates, Genentech, GPS and PDMA group functions. EpiCX Content Management is an integral part of the digital supply chain Veeva Vault PromoMats is the platform and application that EpiCX Content is delivering. It is the single source of truth for Promotional and Non-Promotional content that will be shared between global, affiliates, and...
Jan 16, 2021
About EpiCX EpiCX, the Global Customer Engagement Program, is a business and IT transformation program, currently in flight and planned to be completed in 2023 across 100+ affiliates. Its main ambition is to add meaning and value to all Roche's customer interactions through a single, common, customer-centric technology ecosystem. The EpiCX program will develop and deploy an enterprise-wide ecosystem which integrates world-class orchestrated customer engagement, content management, data and analytics products into one harmonized, centralized and scalable technology ecosystem. This ecosystem will run across all Roche Pharma affiliates, Genentech, GPS and PDMA group functions. EpiCX Content Management is an integral part of the digital supply chain Veeva Vault PromoMats is the platform and application that EpiCX Content is delivering. It is the single source of truth for Promotional and Non-Promotional content that will be shared between global, affiliates, and...
Genentech, a member of the Roche Group, is looking for an experienced, collaborative attorney to join our Legal Department as Senior Counsel, Privacy Law. In this role, you will report to the company's Chief Privacy Officer in the Privacy Law Group, and will be responsible for advising on and promoting compliance with data protection and privacy laws and regulations affecting business activities primarily in the United States. You will develop and implement related policies, practices, and training programs, and help business stakeholders to understand and address data protection and privacy issues as they emerge in the development of new products and technologies. You will be expected to stay abreast of developments and trends in data protection and privacy laws and regulations and enforcement. Responsibilities: Act as a key internal point-of-contact and subject matter expert on all matters relating to privacy law, including providing practical, timely, strategic, and...
Jan 16, 2021
Genentech, a member of the Roche Group, is looking for an experienced, collaborative attorney to join our Legal Department as Senior Counsel, Privacy Law. In this role, you will report to the company's Chief Privacy Officer in the Privacy Law Group, and will be responsible for advising on and promoting compliance with data protection and privacy laws and regulations affecting business activities primarily in the United States. You will develop and implement related policies, practices, and training programs, and help business stakeholders to understand and address data protection and privacy issues as they emerge in the development of new products and technologies. You will be expected to stay abreast of developments and trends in data protection and privacy laws and regulations and enforcement. Responsibilities: Act as a key internal point-of-contact and subject matter expert on all matters relating to privacy law, including providing practical, timely, strategic, and...
Position Summary Commercial Regulatory Affairs (CORA) is part of the broader Product Development Regulatory (PDR) organization that interprets the needs of worldwide health authorities and provides regulatory intelligence necessary to generate and present information that meets the needs of health authorities, patients, purchasers and prescribers for Roche's global Pharma Division, which includes all therapeutic areas and all phases of product development from early development to post-marketing. PDR is responsible for the timely submission of applications to health authorities for approval of new products and line extensions. PDR is committed to regulatory strategies that are the most innovative, ethical, and influential in the industry. The CORA Department reports into the Head of U.S. Regulatory Affairs and is focused on the U.S. Market. Associate Program Directors of Program Review Committees (PRCs) provide regulatory support for the assigned products or...
Jan 16, 2021
Position Summary Commercial Regulatory Affairs (CORA) is part of the broader Product Development Regulatory (PDR) organization that interprets the needs of worldwide health authorities and provides regulatory intelligence necessary to generate and present information that meets the needs of health authorities, patients, purchasers and prescribers for Roche's global Pharma Division, which includes all therapeutic areas and all phases of product development from early development to post-marketing. PDR is responsible for the timely submission of applications to health authorities for approval of new products and line extensions. PDR is committed to regulatory strategies that are the most innovative, ethical, and influential in the industry. The CORA Department reports into the Head of U.S. Regulatory Affairs and is focused on the U.S. Market. Associate Program Directors of Program Review Committees (PRCs) provide regulatory support for the assigned products or...
The Business Management group's vision is to provide the most efficient and strategic business solutions for Development Sciences (DevSci). The Senior Business Manager will contribute to the success of DevSci by leading/managing strategic planning activities and providing business management support to key scientific functions, managing essential cross-functional projects, as well as taking ongoing responsibility for certain key business processes. The Business Management group ensures effective management of a wide range of projects and processes, for ~500 scientists and managers, in such areas as: Partnering with functional area heads (VP/Director-level) to enable them to meet functional goals and improve operational capabilities Being a thought-partner and advisor to DevSci leaders on business, organizational, and operational strategies and solutions Planning and implementing functional and cross-functional initiatives and deliverables Leading or managing DevSci...
Jan 16, 2021
The Business Management group's vision is to provide the most efficient and strategic business solutions for Development Sciences (DevSci). The Senior Business Manager will contribute to the success of DevSci by leading/managing strategic planning activities and providing business management support to key scientific functions, managing essential cross-functional projects, as well as taking ongoing responsibility for certain key business processes. The Business Management group ensures effective management of a wide range of projects and processes, for ~500 scientists and managers, in such areas as: Partnering with functional area heads (VP/Director-level) to enable them to meet functional goals and improve operational capabilities Being a thought-partner and advisor to DevSci leaders on business, organizational, and operational strategies and solutions Planning and implementing functional and cross-functional initiatives and deliverables Leading or managing DevSci...
In this role you are a member of our Business Intelligence & Intelligent Search team and a participant of an active local community of IT experts also from other areas of expertise. We are providing global end-to-end Information Insight Services and our accountability includes, among others, provisioning of innovative cloud-based data service solutions for Business Intelligence and Advanced Analytics Our mission is to go beyond our state-of-the-art BI Enterprise capabilities and enable our business and IT partners through cutting-edge innovations and new technologies. In this role you drive activities, initiatives, programs and projects for Cloud Enablement, SaaS Strategies, and related Data Services in our scope. While your primary tasks are about stakeholder engagement, the consultancy and broad adoption of new cloud-based Data Services in the context of Analytics and Business Intelligence, the role holder should also feel comfortable with organizing and supervising the...
Jan 14, 2021
In this role you are a member of our Business Intelligence & Intelligent Search team and a participant of an active local community of IT experts also from other areas of expertise. We are providing global end-to-end Information Insight Services and our accountability includes, among others, provisioning of innovative cloud-based data service solutions for Business Intelligence and Advanced Analytics Our mission is to go beyond our state-of-the-art BI Enterprise capabilities and enable our business and IT partners through cutting-edge innovations and new technologies. In this role you drive activities, initiatives, programs and projects for Cloud Enablement, SaaS Strategies, and related Data Services in our scope. While your primary tasks are about stakeholder engagement, the consultancy and broad adoption of new cloud-based Data Services in the context of Analytics and Business Intelligence, the role holder should also feel comfortable with organizing and supervising the...
Roche's Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II - IIIA) clinical strategies and plans to deliver medically-differentiated therapies that provide meaningful improvement to patients. The PD Clinical Science Associate participates in development of the Clinical Development (CD) plan and supports the assigned PD Medical Director/Clinical Development Physician(s) with various deliverables necessary for effective and efficient CD plan execution for the assigned molecule(s)/indication(s). PD Clinical Scientists have primary responsibilities for supporting PD Medical Directors/Clinical Development Physicians with clinical documentation, representing CD on various sub-teams or other appropriate forums, supporting training of study site personnel, acting as a primary point-of-contact for questions and inquiries to CD regarding CD studies or other programs, conducting ongoing...
Jan 12, 2021
Roche's Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II - IIIA) clinical strategies and plans to deliver medically-differentiated therapies that provide meaningful improvement to patients. The PD Clinical Science Associate participates in development of the Clinical Development (CD) plan and supports the assigned PD Medical Director/Clinical Development Physician(s) with various deliverables necessary for effective and efficient CD plan execution for the assigned molecule(s)/indication(s). PD Clinical Scientists have primary responsibilities for supporting PD Medical Directors/Clinical Development Physicians with clinical documentation, representing CD on various sub-teams or other appropriate forums, supporting training of study site personnel, acting as a primary point-of-contact for questions and inquiries to CD regarding CD studies or other programs, conducting ongoing...
Roche's Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II - IIIA) clinical strategies and plans that deliver medically-differentiated therapies that provide meaningful improvement to patients. The PD Medical Director participates in development of the Clinical Development (CD) strategy and is responsible for developing the CD plan and ensuring effective and efficient CD plan execution for the assigned molecule(s)/indication(s). PD Medical Directors may have one or more direct reports. PD Medical Directors are expected to perform their responsibilities with more independence by comparison to Associate PD Medical Directors, including participating in health authority (HA) interactions with little to no supervision from their managers. PRIMARY DUTIES AND RESPONSIBILITIES: 1. Cross-Functional Team Leadership & People Management • Participates in and/or leads the relevant Clinical...
Jan 12, 2021
Roche's Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II - IIIA) clinical strategies and plans that deliver medically-differentiated therapies that provide meaningful improvement to patients. The PD Medical Director participates in development of the Clinical Development (CD) strategy and is responsible for developing the CD plan and ensuring effective and efficient CD plan execution for the assigned molecule(s)/indication(s). PD Medical Directors may have one or more direct reports. PD Medical Directors are expected to perform their responsibilities with more independence by comparison to Associate PD Medical Directors, including participating in health authority (HA) interactions with little to no supervision from their managers. PRIMARY DUTIES AND RESPONSIBILITIES: 1. Cross-Functional Team Leadership & People Management • Participates in and/or leads the relevant Clinical...
The Position: The growing gRED IT Lab Engineering, Automation & Productivity (LEAP) group supports the IT needs of Genentech's Research and Early Development (gRED) laboratories. LEAP seeks an inspirational and talented leader to grow and lead a team of Informatics professionals consisting of technical project managers, business systems analysts, and technical leads. Your responsibilities will include working across a diverse team of scientists and IT professionals to manage the operations, development, support and evolution of LEAP solutions supporting R&D labs within the gRED organization. You will join a growing LEAP team with a variety of skills and experiences in both technology and life sciences. Together you will have the opportunity to shape and build a modern R&D environment that propels Genentech's drug development ambitions. Genentech provides an exceptional research environment composed of internationally recognized leaders, state of the art core...
Jan 10, 2021
The Position: The growing gRED IT Lab Engineering, Automation & Productivity (LEAP) group supports the IT needs of Genentech's Research and Early Development (gRED) laboratories. LEAP seeks an inspirational and talented leader to grow and lead a team of Informatics professionals consisting of technical project managers, business systems analysts, and technical leads. Your responsibilities will include working across a diverse team of scientists and IT professionals to manage the operations, development, support and evolution of LEAP solutions supporting R&D labs within the gRED organization. You will join a growing LEAP team with a variety of skills and experiences in both technology and life sciences. Together you will have the opportunity to shape and build a modern R&D environment that propels Genentech's drug development ambitions. Genentech provides an exceptional research environment composed of internationally recognized leaders, state of the art core...
We have an opportunity available for an exceptional individual who can contribute to and drive specific aspects of process development and optimization of the rapidly developing field of cell therapy to support clinical trials and commercialization. The expectation is to find a highly motivated individual who is keenly interested in helping build an industry leading cell therapy group. The job responsibility consists of hands-on lab work optimizing T-cell culture at small-scale and representative-scale production, technology transfer to a CDMO and subsequent optimization of these workflows in-house. Strong molecular biology background would be highly desired to help contribute to process optimization of non-viral gene editing and plasmid manufacturing. The selected individual will contribute to and drive scientific discussions, design experiments and troubleshoot, and generate reliable and high-quality data to help make key decisions. Expectations also include...
Jan 10, 2021
We have an opportunity available for an exceptional individual who can contribute to and drive specific aspects of process development and optimization of the rapidly developing field of cell therapy to support clinical trials and commercialization. The expectation is to find a highly motivated individual who is keenly interested in helping build an industry leading cell therapy group. The job responsibility consists of hands-on lab work optimizing T-cell culture at small-scale and representative-scale production, technology transfer to a CDMO and subsequent optimization of these workflows in-house. Strong molecular biology background would be highly desired to help contribute to process optimization of non-viral gene editing and plasmid manufacturing. The selected individual will contribute to and drive scientific discussions, design experiments and troubleshoot, and generate reliable and high-quality data to help make key decisions. Expectations also include...
Job Summary: Reporting to the Head of Global Quality Control this position is responsible, in collaboration with cross functional stakeholders, for the commercial QC strategy for ATMP products and implementing the strategy into respective QC network locations. The scope of programs includes viral vector based Gene Therapy, gene edited Cell Therapy, neo-antigen based mRNA therapy and other modalities that are classified as ATMPS. The QC elements include collaboration (with a strong focus on facilitating technical implementation) with development teams on control considerations for ATMP programs, defining the commercial control system, evaluation of stability program requirements, establishment of risk-based assessment of product quality attributes, evaluation of appropriateness of the specification, consultation on rapid microbial methods that support the safety of small volume to single patient batches, and the evaluation of appropriateness, and recommendation for management...
Jan 10, 2021
Job Summary: Reporting to the Head of Global Quality Control this position is responsible, in collaboration with cross functional stakeholders, for the commercial QC strategy for ATMP products and implementing the strategy into respective QC network locations. The scope of programs includes viral vector based Gene Therapy, gene edited Cell Therapy, neo-antigen based mRNA therapy and other modalities that are classified as ATMPS. The QC elements include collaboration (with a strong focus on facilitating technical implementation) with development teams on control considerations for ATMP programs, defining the commercial control system, evaluation of stability program requirements, establishment of risk-based assessment of product quality attributes, evaluation of appropriateness of the specification, consultation on rapid microbial methods that support the safety of small volume to single patient batches, and the evaluation of appropriateness, and recommendation for management...
The Position Development Sciences Informatics is seeking a talented and experienced informatics engineer to develop scientific software tools, software engineering, bioinformatics algorithm design, pipeline development and implementation. You will provide engineering leadership in collaboration with scientists and other engineers to facilitate deep exploration of multidimensional preclinical and clinical omics data. You should have a flexible and learning mindset, be able to work in a fluid and dynamic environment, be comfortable leading globally distributed development teams and have a strong desire to pursue creative solutions to challenging problems. In this job, you will design and develop scientific databases, and create methods to process and analyze omics data or other biological information. Additionally, you will lead application development efforts and establish data engineering platforms to enable the storage, organization, dissemination, and analytics of dynamic data...
Jan 08, 2021
The Position Development Sciences Informatics is seeking a talented and experienced informatics engineer to develop scientific software tools, software engineering, bioinformatics algorithm design, pipeline development and implementation. You will provide engineering leadership in collaboration with scientists and other engineers to facilitate deep exploration of multidimensional preclinical and clinical omics data. You should have a flexible and learning mindset, be able to work in a fluid and dynamic environment, be comfortable leading globally distributed development teams and have a strong desire to pursue creative solutions to challenging problems. In this job, you will design and develop scientific databases, and create methods to process and analyze omics data or other biological information. Additionally, you will lead application development efforts and establish data engineering platforms to enable the storage, organization, dissemination, and analytics of dynamic data...
The Senior Engineer - Single Use Consumables Expert is an integral member of the Clinical Supply Center (CSC) team in South San Francisco (SSF). The SSF CSC is designed to be a state-of-the-art large molecule drug substance facility which supports GMP production for phase 1, 2 and early phase 3 clinical trials. The CSC will employ a ballroom design, utilize single-use technology, new analytical techniques and digital manufacturing systems to deliver a best in class bioprocess facility. We are looking for individuals to support this facility who are comfortable with ambiguity, have an entrepreneurial spirit within a GMP environment, have demonstrated strong Pharma Technical Behaviors, and have an agile mindset. Ability to collaborate is crucial as success will be measured as a member of a team, not just as an individual. Ideal candidates would have experience in a broad range of functional roles in support of biopharmaceutical production. In this role the qualified individual...
Jan 08, 2021
The Senior Engineer - Single Use Consumables Expert is an integral member of the Clinical Supply Center (CSC) team in South San Francisco (SSF). The SSF CSC is designed to be a state-of-the-art large molecule drug substance facility which supports GMP production for phase 1, 2 and early phase 3 clinical trials. The CSC will employ a ballroom design, utilize single-use technology, new analytical techniques and digital manufacturing systems to deliver a best in class bioprocess facility. We are looking for individuals to support this facility who are comfortable with ambiguity, have an entrepreneurial spirit within a GMP environment, have demonstrated strong Pharma Technical Behaviors, and have an agile mindset. Ability to collaborate is crucial as success will be measured as a member of a team, not just as an individual. Ideal candidates would have experience in a broad range of functional roles in support of biopharmaceutical production. In this role the qualified individual...
We are looking for a highly motivated Quality Engineer to represent Quality as a member of the Drug Substance Manufacturing Execution System (MES) CORE Team. The Drug Substance network is embarking on implementation of a single MES system at six manufacturing sites. The successful candidate will support the Drug Substance network MES CORE user requirements definition, partner with Pharma Informatics Drug Substance Manufacturing, and support the Validation Lead for CSV and deployment strategy. This person will partner with personnel at the Drug Substance manufacturing sites to align quality business processes (e.g., review by exception, electronic batch production records/batch reports, materials management, sample management) and to facilitate implementation of new GMP manufacturing and quality systems from the IT/OT roadmap. This role will report directly to the Head of Quality Drug Substance. Job Responsibilities Partner with the Drug Substance MES CORE product owner to...
Jan 07, 2021
We are looking for a highly motivated Quality Engineer to represent Quality as a member of the Drug Substance Manufacturing Execution System (MES) CORE Team. The Drug Substance network is embarking on implementation of a single MES system at six manufacturing sites. The successful candidate will support the Drug Substance network MES CORE user requirements definition, partner with Pharma Informatics Drug Substance Manufacturing, and support the Validation Lead for CSV and deployment strategy. This person will partner with personnel at the Drug Substance manufacturing sites to align quality business processes (e.g., review by exception, electronic batch production records/batch reports, materials management, sample management) and to facilitate implementation of new GMP manufacturing and quality systems from the IT/OT roadmap. This role will report directly to the Head of Quality Drug Substance. Job Responsibilities Partner with the Drug Substance MES CORE product owner to...
Development Sciences Informatics is seeking a talented and experienced solution architect to drive the application development efforts that assist in discovering groundbreaking therapeutics . You will lead data platform architecture initiatives in a hybrid-cloud environment. You will provide engineering leadership in collaboration with scientists and other engineers to facilitate deep exploration of multidimensional preclinical and clinical data. You should have a flexible and learning mindset, be able to work in a fluid and dynamic environment, be comfortable leading globally distributed development teams and have a strong desire to pursue creative solutions to challenging problems. Establish and maintain the technical and scientific partnership with scientific functions. Communicate effectively with key stake holders. Contribute to strategic planning and implementation of our data engineering platforms for multiple functions to ensure data accessibility, quality, and integrity....
Dec 25, 2020
Development Sciences Informatics is seeking a talented and experienced solution architect to drive the application development efforts that assist in discovering groundbreaking therapeutics . You will lead data platform architecture initiatives in a hybrid-cloud environment. You will provide engineering leadership in collaboration with scientists and other engineers to facilitate deep exploration of multidimensional preclinical and clinical data. You should have a flexible and learning mindset, be able to work in a fluid and dynamic environment, be comfortable leading globally distributed development teams and have a strong desire to pursue creative solutions to challenging problems. Establish and maintain the technical and scientific partnership with scientific functions. Communicate effectively with key stake holders. Contribute to strategic planning and implementation of our data engineering platforms for multiple functions to ensure data accessibility, quality, and integrity....
The Discovery Proteomics group is seeking an experienced Scientist/Senior Scientist with a record of high impact research involving mass spectrometry proteomics to join the group, develop an independent research program, and guide collaborative investigations. Advances in mass spectrometry proteomics have revolutionized the study of cellular proteins and motivated in depth molecular characterization of normal human physiology and disease biology. The Discovery Proteomics group develops and implements protein analytical methods to differentiate between dynamic biological states by characterizing the abundance, dynamics and interactions of proteins. As is true across Genentech, research in the group is fast paced and highly collaborative, drawing on the expertise of some of the world's leading experts in biochemistry, cell biology and disease indications. For more information on the Kirkpatrick Lab see: https://www.gene.com/scientists/our-scientists/don-kirkpatrick Who You Are...
Dec 25, 2020
The Discovery Proteomics group is seeking an experienced Scientist/Senior Scientist with a record of high impact research involving mass spectrometry proteomics to join the group, develop an independent research program, and guide collaborative investigations. Advances in mass spectrometry proteomics have revolutionized the study of cellular proteins and motivated in depth molecular characterization of normal human physiology and disease biology. The Discovery Proteomics group develops and implements protein analytical methods to differentiate between dynamic biological states by characterizing the abundance, dynamics and interactions of proteins. As is true across Genentech, research in the group is fast paced and highly collaborative, drawing on the expertise of some of the world's leading experts in biochemistry, cell biology and disease indications. For more information on the Kirkpatrick Lab see: https://www.gene.com/scientists/our-scientists/don-kirkpatrick Who You Are...
Job Knowledge & Scope Roche is pioneering advanced analytics tools to develop deeper understanding of our cell culture processes. We are looking for a highly motivated and scientifically minded person to advance our transient and stable gene expression platforms. This position will be an integral part of our Research Material Generation team to advance our innovative efforts, speed up our development processes, and get our medicines to patients faster. This position in the Cell Culture and Bioprocess Operations department will focus on the development and characterization of cell culture processes for the production of recombinant proteins in CHO and HEK293 cells. Primary responsibilities include developing, improving and troubleshooting cell culture processes to deliver diverse protein and cellular reagents to enable a large number of research programs. Close collaboration with fellow scientists in cell culture, protein engineering, molecular biology, structural...
Dec 25, 2020
Job Knowledge & Scope Roche is pioneering advanced analytics tools to develop deeper understanding of our cell culture processes. We are looking for a highly motivated and scientifically minded person to advance our transient and stable gene expression platforms. This position will be an integral part of our Research Material Generation team to advance our innovative efforts, speed up our development processes, and get our medicines to patients faster. This position in the Cell Culture and Bioprocess Operations department will focus on the development and characterization of cell culture processes for the production of recombinant proteins in CHO and HEK293 cells. Primary responsibilities include developing, improving and troubleshooting cell culture processes to deliver diverse protein and cellular reagents to enable a large number of research programs. Close collaboration with fellow scientists in cell culture, protein engineering, molecular biology, structural...
