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452 jobs match your search criteria:
| Date | Job Title | Job Level | Location | |
|---|---|---|---|---|
| Mar 1, 2013 |
Sr Business Sys Analyst
The IT Business Systems Analyst position will be responsible for working closely with partners across lines of business and the IT group in order to understand strategic drivers and tactical needs to ensure that implementation teams can provide solutions that meet the business need with the necessary stability, usability, and scalability. The IT Business Systems Analyst will be supporting projects in the global Laboratory Information Management Solutions portfolio for manufacturing and clinical Quality Control laboratories. Duties:
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Experienced | South San Francisco, California | |
| May 23, 2013 |
Senior Scientific Manager, Translational Immunology
Genentech has an opportunity for a Senior Scientific Manager to oversee the operation of the Translational Immunology group.
Responsiblities Include:
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Manager | South San Francisco, California | |
| Mar 6, 2013 |
Utility Plant Operator
• Operate all utility systems and utility subsystems at Genentech, SSF
• Ensure all utility systems and utility subsystems at Genentech, SSF are operated and maintained in the following manner: ¿ All preventative maintenance is performed at the appropriate interval and is completed by the assigned due date. ¿ All equipment remains in its designed and/or validated state at all times ¿ All equipment operation is in accordance with Federal, State, local, and Genentech regulations, procedures, and policies • Ensure/maintain all utility equipment areas in a constant state of inspection readiness; specifically but not limited to the following: ¿ Cleanliness ¿ Personnel and Equipment Safety ¿ Compliance to cGMP requirements • Continuously evaluate the operation of all utility systems and utility subsystems at Genentech SSF. Identify specific process improvement needs and provide recommendations for system upgrades. • Troubleshoots, maintains, inspects and repairs heating, ventilation systems, air conditioning and refrigeration systems and equipment including DX and hydronics systems and components, screw, reciprocating and absorption chillers, cooling towers, fans and fan motors, pumps and pump motors, electric controls and associated safety, overcurrent and other equipment protection devices. • Identify training deficiencies, provide recommendations for training and where applicable provide training. • Continuously evaluate all operational Standard Operating Procedures and Preventive Maintenance procedures for accuracy and applicability. Submit appropriate change requests through the Faciltiy Services Document Tracking Database to correct any deficiencies discovered. • Provide operational support to Facility Services, Engineering, Manufacturing, and Research and Development. This support must not interfere with the normal day to day operation of any utility systems and utility subsystems at Genentech SSF. • Perform Confined Space Entry on an as needed basis. • Complete preventive maintenance and assigned paperwork in a timely manner following all cGMP documentation guidelines. • Responsible for gathering and documenting the appropriate information associated with a System Discrepancy, (An event in manufacturing process and/or support system that is outside approved operating parameters or approved proceures). • Work with various chemicals, steam, pressurized gases/liquids of various temperatures. • Work in close proximity to moving equipment. • Conduct work in an FDA regulated environment.... |
Experienced | South San Francisco, California | |
| Jan 14, 2013 |
Senior Manager - ERP Demand & Production Services
The ERP Demand & Production Services team is part of the ERP Demand-to-Supply (D2S) team within the Pharma Informatics Shared Platforms & Applications - ERP organization. This global team provides SAP and non-SAP-based solutions and services to our Global Supply Chain (Clinical & Commercial) business function. These solutions include: SAP’s APO (Advanced Planner & Optimizer), SNC (Supplier Network Collaboration), OER (Object Event Repository), AII (Auto-ID Infrastructure), and other vendor and custom solutions, along with integration to various manufacturing and other supply chain solutions. The Head of ERP Demand & Production Services will provide global perspective and partnership and leverage knowledge across the Roche Group in order to better enable our Supply Chain business to achieve their goals. They will also drive customer demand management, people management, project management, solution development, maintenance, enhancement, and operational support. In collaboration with the business, they will develop strategies and plans that maximize the ROI from the use of our solutions. The Head of ERP Demand & Production Services is accountable for the management and leadership of a team of IT professionals located in Basel, Switzerland and South San Francisco, California, USA, along with the management of shared services resources in Poland and outsource resources - both onsite and offsite. This position can be based in Basel, Switzerland or South San Francisco, California. As a member of the ERP D2S Leadership team, the Head of ERP Demand & Production Services will:
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Manager with Direct Reports | South San Francisco, California | |
| May 28, 2013 |
Automation Engineer - Process Development Engineering
Level:
The Automation Engineer will be expected to support the users and systems in the large scale cell culture pilot plant. This role will require design, specification, implementation and maintenance of bioreactor control systems for both mammalian and microbial processes. Key roles and responsibilities include:
- Maintenance and troubleshooting of hardware and software on the process control systems in the Process R&D Labs and pilot plants. - Design, implementation and support of laboratory automation systems. - Leading and supporting small project teams which design develop and integrate automation systems in the Process R&D laboratory and pilot plants. - Scope of work definition and supervision of contract labor for small and medium projects under the direction of a senior engineer. - Collaboration with Corporate Engineering, Manufacturing Science and Technology (MSAT) and other business partner groups on technology transfers and information exchanges. - Author and maintain system support and specification documentation. - Author technical reports and/or presentations. - 24/7 on-call support is required for this position.
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Experienced | South San Francisco, California | |
| Feb 15, 2013 |
Statistical Programmer Analyst
Statistical Programmer (SPA-2) Position Purpose: The Statistical Programmer has responsibility for statistical programming support for the Pharma Development, gRED, pRED, and/or EpiPRO organizations. He/she supports statistical programming teams on assigned study level activities in planning, designing, and implementing statistical software solutions for the reporting and analysis of clinical trials in accordance with applicable processes. Major Responsibilities and Accountabilities: Contributes to SPA team in preparing summarized information to clinical study team members Assist statistical programming activities at study level or components of a clinical project as applicable Able to access and clarify requirements, provide statistical programming solutions and ensure their efficient implementations under supervision Under guidance of a senior SPA, develops approaches to meet the study and project requirements Assist in determining and developing approach to technical solutions Responsible for accuracy and reliability of results. Builds and monitors quality in every aspect of job activities. Has an awareness and familiarity with the types of risks associated with a study and the impact on the quality of deliverables Is aware of timelines and scope based on resourcing / priority constraints within the SPA team and understand their implications on individual work assignments Builds and maintains effective working relationships with SPA team members. Adapts to changing circumstances, policies, work assignments, and/or team members. Able to multi-task and prioritize between tasks ... |
Experienced | South San Francisco, California | |
| May 20, 2013 |
Scientist
RESPONSIBILITIES: A Scientist or Sr. Scientist position is being offered to a highly motivated, qualified candidate to join the Marketed Product Support Group in the Late Stage Pharmaceutical Development Department. The position is Responsible for manufacturing site transfer and line extensions for the Genentech legacy biologics drug products, serves as technical subject matter experts for Quality investigations related to manufacturing and customer complaints, contributes to the relevant regulatory filings, supports the Quality organization during health authority inspections and for commercial control system upgrades. The individual will participate in multi-functional product technical teams and will work closely with personnel within and outside the Late Stage Pharmaceutical Development Department. ... |
Experienced | South San Francisco, California | |
| Jan 22, 2013 |
Senior Project Manager - IT Research & Development
This IT Manager is responsible for managing the Portfolio processes for Research and Development IT and for providing Project Management on a variety of projects that are used by Research and Early Development. The position also oversees Portfolio/Project Management, Budgeting, Forecasting and related processes for Research and Development IT. The position is part of the gRED IT organization. Responsibilities:
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Experienced | South San Francisco, California | |
| Jan 17, 2013 |
Staff Statistical Scientist
Global Product Development Biometrics Biostatistics (PDBB) at Roche/Genentech plays a key role in successful drug development by contributing expertise to the drug development process from research through entry into humans through regulatory approval and beyond. Biostatisticians collaborate on cross-functional teams with colleagues from Clinical Science, Safety Science, Regulatory Affairs, and other functions. Statistical Methods and Research is a group of statisticians within PDBB with a mission to enhance our strategic and methodological capabilities. Current areas include portfolio decision-making, quantitative benefit-risk, regulatory statistics, and personalized healthcare, but may be extended to meet business needs. Key responsibilities include: • Provide effective, timely and reliable consultancy across the company on statistical problems • Engage in research in statistics to improve clinical trial methodology used in the development of company products consistent with corporate priorities and timelines • Work in collaboration with Biostatistics leadership to identify and prioritize areas of potential impact that need new or improved statistical methods • Impact drug development science beyond the company in industry forums • Influence internal and external stakeholders to produce and implement robust drug development strategies • Contribute to ensure that PDBB is regarded as highly effective strategic partners in drug development whose prestige extends beyond the company • Develop and maintain expertise in at least one core area of biostatistics and serve as an advisor to other biostatisticians and PD leadership ... |
Experienced | South San Francisco, California | |
| May 20, 2013 |
Clinical Scientist Hematology, GDC 0199
Provides clinical oversight for a variety of projects, in consultation with his/her Medical Director or Senior Medical Director : · Works with a host of internal and external partners and stakeholders in the implementation of clinical trials for assigned drugs/indication · Provides scientific input into and/or coordinates the development of specific clinical trial documents for review and discussion with Medical Directors* (e.g., protocols, charters, safety monitoring plans, process documents, etc.) including disease and/or treatment registries · Participates in the identification of appropriate external investigators · Oversees the clinical trial implementation, ongoing monitoring and evaluation, working closely and regularly with external investigators and Clinical Operations. Active Member in Study Management Team for assigned drugs/indications · Develops and cultivates relationships with external partners such as clinical investigators, clinicians, scientists and KOLs, as well as cross-functional partners in Clinical Development, Commercial, Legal and Regulatory. · Supports his/her manager in developing clinical components of presentations* for clinical trial investigator meetings · In collaboration with his/her manager, coordinates the preparation and reviews data outputs for reporting documents* where appropriate (e.g. clinical study reports, analysis plans, etc.) with the CRO, the Medical Affairs Biostatisticians and his/her Medical Directors · Monitors project progress and is expected to proactively identify any issues or challenges and recommend and implement strategies to effectively resolve such once approved with his/her manager · Works closely with his/her manager, the publication team and Clinical Operations to complete associated publications, reviews draft publications*. · Keeps all partners abreast of projects progress throughout all applicable intervals · May also participate/coordinate collaborations with external stakeholders (e.g. cooperative groups, other companies, etc.) on development and implementation of approved clinical projects. · May coordinate, liaise with internal and external providers for data mining activities · Helps his/her manager provide data outputs requested for safety and/or other relevant sections of IND annual reports, if these sections and reports relate to assigned drugs and/or indications*. · May interact with NCI or other agency, as appropriate, with supervision from his/her manager
¿ Stays abreast of internal and external developments (scientific, clinical, commercial, competitive, legal, regulatory and like) as such developments may implicate or otherwise impact the implementation of the medical plan of the assigned drug(s)/indication(s). Includes attendance at major scientific conferences, participation in competitive intelligence activities, and review of published literature ... |
Experienced | South San Francisco, California | |
| May 20, 2013 |
Product Manager/Sr. Product Manager, Account Team - MC Marketing
Product Manager or Sr. Product Manager Senior Product Managers in Managed Care Marketing develop, implement and manage the managed care marketing strategy, plan and tactics for the assigned managed care segments in the U.S. and related territories . Managed Care Marketing directly supports Genentech’s business by ensuring managed care marketing strategies, plans and tactics enable business, financial and operational goals, targets and objectives to be met or exceeded across managed care segments within the U.S. Senior Product Managers act as a primary liaison to managed care account management in the assigned managed care segments and may also have matrix responsibilities to represent Managed Care Marketing for one or more products or franchises, as assigned. This role is focused on customer-specific pull-through through use of marketing tools and resources, including application of Value-based Healthcare, promotional, B2B, brand and other relevant resources for key accounts
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Experienced | South San Francisco, California | |
| Apr 16, 2013 |
Sr. Project Mgr, PMO (gRED)
We are seeking a Sr. Project Manager who will manage complex projects to successful and timely decision points from Late Stage Research through Proof of Concept. The Sr. Project Manager will actively contribute to the definition of project strategy and guide the project core and sub teams to deliver on project objectives. This position will be accountable for steering drug development teams through corporate processes. Additional responsibilities include but are not limited to the following:
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Manager | South San Francisco, California | |
| Jun 3, 2013 |
Medical Science Liaison - Arizona, New Mexico, San Diego, Orange County, and Southern Nevada
MSL-Oncology The states covered are Arizona, New Mexico, San Diego, Orange County, and Southern Nevada Main Purpose of the Position:
Job Duties/Responsibilities: General:
Clinical trial support: MSLs interact with Genentech Medical Directors and their designees to determine and coordinate health care practitioner, researcher, and investigator activities.. MSLs act as the conduit between external customers and the Genentech Medical Directors.
Customer/Investigator support:
Commercial support: |
Experienced | South San Francisco, California | |
| Mar 20, 2013 |
Clinical Scientist Specialist - TDM1
Provides clinical oversight for a variety of projects, in consultation with his/her Medical Director or Senior Medical Director : · Works with a host of internal and external partners and stakeholders in the implementation of clinical trials for assigned drugs/indication · Provides scientific input into and/or coordinates the development of specific clinical trial documents for review and discussion with Medical Directors* (e.g., protocols, charters, safety monitoring plans, process documents, etc.) including disease and/or treatment registries · Participates in the identification of appropriate external investigators · Oversees the clinical trial implementation, ongoing monitoring and evaluation, working closely and regularly with external investigators and Clinical Operations. Active Member in Study Management Team for assigned drugs/indications · Develops and cultivates relationships with external partners such as clinical investigators, clinicians, scientists and KOLs, as well as cross-functional partners in Clinical Development, Commercial, Legal and Regulatory. · Supports his/her manager in developing clinical components of presentations* for clinical trial investigator meetings · In collaboration with his/her manager, coordinates the preparation and reviews data outputs for reporting documents* where appropriate (e.g. clinical study reports, analysis plans, etc.) with the CRO, the Medical Affairs Biostatisticians and his/her Medical Directors · Monitors project progress and is expected to proactively identify any issues or challenges and recommend and implement strategies to effectively resolve such once approved with his/her manager · Works closely with his/her manager, the publication team and Clinical Operations to complete associated publications, reviews draft publications*. · Keeps all partners abreast of projects progress throughout all applicable intervals · May also participate/coordinate collaborations with external stakeholders (e.g. cooperative groups, other companies, etc.) on development and implementation of approved clinical projects. · May coordinate, liaise with internal and external providers for data mining activities · Helps his/her manager provide data outputs requested for safety and/or other relevant sections of IND annual reports, if these sections and reports relate to assigned drugs and/or indications*. · May interact with NCI or other agency, as appropriate, with supervision from his/her manager
¿ Stays abreast of internal and external developments (scientific, clinical, commercial, competitive, legal, regulatory and like) as such developments may implicate or otherwise impact the implementation of the medical plan of the assigned drug(s)/indication(s). Includes attendance at major scientific conferences, participation in competitive intelligence activities, and review of published literature ... |
Experienced | South San Francisco, California | |
| May 13, 2013 |
GNE Principal Compliance Specialist
3 positions available for locations in SSF. Washington DC or Basel
Main Purpose of the Position: · Provides objective and uniform assessments of quality and compliance risks across global network, including independent expert review of (1) the internal GMP auditing program and (2) correspondence to global health authorities regarding GMP issues. · Supports support liaisons and interactions with external bodies and committees to influence on technical quality issues through articles, speeches and participation on committees
Job Duties/Responsibilities: · Performs independent expert assessment to determine global uniformity and conformance to appropriate regulatory standards for (1) internal GMP audits and (2) correspondence to global health authorities regarding GMP issues, including written responses to inspectional observations. · Advise senior management across PT Global network on best practices, regulatory intelligence, key opportunities, and possible threats in the areas of quality and compliance. · Provides up to date regulatory and compliance information and trends, specializing in specific regulatory authorities and regions, providing timely information to the PTQ organization. · Contributes to expert GMP compliance opinions for PT Global network, including Manufacturing, Quality, and Regulatory Affairs. · Participates as a key member of teams throughout the global Technical Operations Quality organization for strategy and policy, external interactions and influencing activities as they relate to Quality and GMP/GDP Compliance · Supports the overall efforts for strong health authority relationships in the areas of Quality and Compliance through effective communications, interactions and participation in meetings, conferences and committees with focus on respective region or area of expertise. ... |
Experienced | South San Francisco, California | |
| Feb 8, 2013 |
Sr. Engineer/Sr. Manufacturing Technical Specialist, Biologics Manufacturing Science and Technology, Drug Product
This position is part of the drug product group within Biologics Manufacturing Science and Technology (BMSAT) organization. The successful candidate will work with a team of engineers and manufacturing technical specialist responsible for fill-finish technology transfer to contract/partner manufacturing sites, as well as process transfer between Genentech/Roche manufacturing sites. The successful candidate will also be responsible for providing ongoing technical support for drug product manufacturing processes across the Genentech/Roche network. Candidate will ensure technical stewardship across the various CMO product transfers as well as ongoing continuous improvement projects.
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Experienced | South San Francisco, California | |
| May 7, 2013 |
Senior Manager, Internal Communications, Corporate Relations - Functional & Executive Communications
Senior Manager, Internal Communications, Corporate Relations The Position The Senior Manager, Internal Communications, reports to the Director of Internal Communications within the Corporate Relations function. This position is responsible for providing internal organizational communications consultation and support to (1) Genentech’s Chief Financial Officer and (2) the Senior Vice President, Secretary and Chief Compliance Officer, Genentech and head of Legal Affairs, North America. In addition, this position is responsible for consulting on communications initiatives from these and other G&A functions to our approximately 12,000 employees, and will play a key role in developing business communications for leaders and for key best companies submissions. This individual will interact with the company’s senior executives as well as with peers in Internal Communications, Corporate Relations and internal communicators throughout Genentech and Roche. Responsibilities
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Experienced | South San Francisco, California | |
| May 6, 2013 |
Non-interventional Program (NIP) Coordinator
Summary of Position: The non-interventionalprogram (NIP) Coordinator is the specific point of contact for requestsregarding NIPs. The NIP Coordinatorensures that all NIPs conducted by Genentech are approved, tracked, andconducted in accordance with relevant regulations and company internalprocesses and procedures.
Job Duties/Responsibilities:
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Experienced | South San Francisco, California | |
| Apr 26, 2013 |
Finance Manager
Finance Manager, FP&A Reporting to the Associate Director, FP&A, the Finance Manager will support the corporate planning processes, including forecast, budget, and long-term planning. This position will be responsible for both delivering forecasts/budgets to local management as well as submission of the plans to Basel. This role will require significant interface with other finance and planning groups across the organization. Job Description:
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Experienced | South San Francisco, California | |
| Apr 29, 2013 |
Network Engineer II
The Network Services Operations team is responsible for project deployment and 24x7 operations support of our North America enterprise wired and wireless networks which serve over 22,000 users and are comprised of wireless access points, switches, routers, firewalls, load balancers, proxies, VPN concentrators, and optical network devices. We are looking for a results-driven analytical thinker with strong technical and process management skills who can provide imaginative, thorough, and practicable technical solutions to a wide range of difficult problems. This person will work closely with our architecture and engineering teams as well as vendors to maintain 99.99% availability while successfully deploying emerging network technologies to new and existing Genentech buildings and data centers. Candidate must have good business acumen and possess strong communication and teamwork skills. We are looking for an individual with strong time management skills who can work autonomously making sound decisions that are consistent with organizational objectives. You must have a proven track record for delivering excellence thus enabling us to meet the scientific demands of our biotechnology revolution in information technologies. ... |
Experienced | South San Francisco, California |
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