Contractor Positions for Roche and Genentech

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Applicants need to be self-motivated, fast learner, critical thinkers, and enthusiastic about science research. Applicants need to work effectively & independently, exhibit a professional manner and establish constructive working relationships. Ability to prioritize task, coordinate tasks with others, and meet the deadlines Hands-on experience performing complex multi-step experiments with detailed and diligent attention to planning, organization, hands-on technique, and record keeping. Proficient in standard molecular biology techniques, which may include sample preparation, nucleic acid purification (RNA/DNA), molecular cloning, PCR and qPCR. Experience with growing and manipulating BSL-2 bacteria is a plus. Good written and oral communication skills including the ability to communicate with all levels within the department. This position primarily involves wet-lab work. You will be expected to perform hands-on research activities at the bench for extended periods each day Independently, or with supervisor's guidance, conduct research, design, plan, and execute innovative and well-controlled experiments with meticulous attention to detail. Ensure that activities align with the project's critical path and adapt to changing priorities as needed. Play an active role in troubleshooting efforts and propose solutions to optimize processes, overcome challenges, and enhance product performance, accuracy, and reliability. Prepare samples and run fully automated cobas X800 instrument for LOD, inclusivity, exclusivity assay test. Maintain accurate, consistent, and timely records of experimental methods, materials, and results in electronic laboratory notebooks. Analyze data, evaluate results, and plan next steps. Integrate previous and current results to determine the next experimental steps and their impact on long-term project goals. Present findings at group or departmental meetings and assist in preparing summaries, memos, internal reports, presentations, manuscripts, and other relevant materials. Collaborate closely with cross-functional teams to ensure effective project progression Stay up-to-date with all training activities.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null, "canonicalPositionUrl": "https://magnitdirectsourcing-rch.magnitglobal.com/careers/job/137458451916", "isPrivate": false}, {"id": 137458424157, "name": "Senior Software Engineer", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1701898886, "t_create": 1701898698, "ats_job_id": 137458424157, "display_job_id": 137458424157, "type": "ATS", "id_locale": "137458424157-en", "job_description": "Senior Software Engineer: Applies knowledge of design principles, practices and implementation in complex systems and assignments. General responsibilities include team leadership and responsibility for the deliverables of a software development team, participating in design reviews, acceptance of team deliverables by assessing performance against design specification and desired customer workflows and outcomes. Participates in a self-organizing team culture. Assist in the delivery of customer-centric features by facilitating and providing servant leadership to a technical team. 8+ years of hands-on experience Full stack developer, working in a Scrum team environment on C# and Delphi technical stack. Experience in Delphi and/or healthcare medical device development a plus.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null, "canonicalPositionUrl": "https://magnitdirectsourcing-rch.magnitglobal.com/careers/job/137458424157", "isPrivate": false}, {"id": 137458424138, "name": "Business Systems Analyst V", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1701898675, "t_create": 1701898390, "ats_job_id": 137458424138, "display_job_id": 137458424138, "type": "ATS", "id_locale": "137458424138-en", "job_description": "You will provide excellent first level and second level (escalations) systems support for both internal and external users that are managing orders, reverse logistics or receiving customer care. You will establish and maintain collaborative partnerships with the team, partners, and vendors to ensure that the Order Management systems are running optimally and efficiently. Systems include; SAP, SalesForce Service Cloud, Hybris, Value Track, Electronic Data Interface (EDI)/Business to Business (B2B) layer and Medallia. You will lead and/or participate in system upgrade, user improvement, technical enhancement or launch readiness projects and facilitate efforts to optimize master data, gather audit information and fulfill reporting requests. You will collect, analyze and synthesize business process and system needs across the team and help to prioritize and communicate these needs to our partners/vendors. You will be solving for ambiguous situations using strong analytical and problem-solving capabilities & skills. You will lead digital projects that explore new ways to use technology to delight end-users and reimagine the customer, employee, and patient experience. You will communicate the current status of systems issues and projects, including timing, prioritization, testing, resource needs, training requirements and process impacts. You are required to have a Bachelor Degree in Information Systems, Engineering or related field with a minimum of 2 to 4+ years' related work experience in business process analysis, systems development, IT project management, preferably gained in the pharmaceutical/biotechnology or related industry. You have a solid understanding and can demonstrate proficiency in the sales portion of the SAP Sales and Distribution (SD) module or other Enterprise Resource Planning (ERP) system. You should have at least 2-3 years of SAP SD or order to cash experience. Additional systems such as Salesforce Service Cloud, Value Track, EDI/B2B are a plus; working IT knowledge, not necessarily a programmer. You demonstrate an orientation to teamwork and customer service and you partner well with others by developing collaborative working relationships. You communicate and present well with a demonstrated ability to communicate complex business and analytical findings to a variety of levels within the organization.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null, "canonicalPositionUrl": "https://magnitdirectsourcing-rch.magnitglobal.com/careers/job/137458424138", "isPrivate": false}, {"id": 137458412035, "name": "Laboratory Technical Specialist I/II", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1701794862, "t_create": 1701790119, "ats_job_id": 137458412035, "display_job_id": 137458412035, "type": "ATS", "id_locale": "137458412035-en", "job_description": "Create an environment of strong team spirit with timely and effective communications. Develop ability to influence using technical and personal reasoning. Perform a broad variety of basic, moderate, and complex tests in support of lab operations, design verification, test method validation, R&D characterization, and complaints investigation. Perform testing of routine and non-routine samples and documents according to cGMPs. Perform routine lab maintenance. Prepare basic and complex reagents as assigned. Perform sample filling and decontamination, and assist in lab complaints investigations. Participate in method transfer and validation. Perform equipment qualification/maintenance as assigned. Coordinate with lab supervisor to support operational activities. Perform other duties as requested by supervisor/manager to support Quality. Work is performed in a laboratory setting. Work requires use of glassware, needles, and syringes. B.S./B.A. (preferably in relevant scientific discipline) or an equivalent combination of education and experience. Basic knowledge of scientific theories, principles, and techniques used in physical and analytical test procedures. Ability to exercise sound judgement, reasoning and problem solving. Capable of completing assigned responsibilities and keeping manager informed of status. Extensive knowledge and technical understanding to complete routine and non-routine assignments. Good verbal and written communication skills needed to accomplish assigned tasks. Ability to work under minimal supervision to complete assigned tasks in a timely manner. Must be highly organized, analytical, detail oriented and able to conduct work independently. Able to conduct work on multiple projects with precision. Team oriented, creative, eager to take on responsibility. Excellent written and verbal communication skills are required. Demonstrated ability to communicate with internal stakeholders and external collaborators. Ability to make repetitive motions and manual manipulations of samples.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null, "canonicalPositionUrl": "https://magnitdirectsourcing-rch.magnitglobal.com/careers/job/137458412035", "isPrivate": false}, {"id": 137458412022, "name": "Purification & Drug Product Pilot Plant Master Technician / Associate Technical Specialist", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1701789990, "t_create": 1701789689, "ats_job_id": 137458412022, "display_job_id": 137458412022, "type": "ATS", "id_locale": "137458412022-en", "job_description": "Routinely perform operations such as cleaning, sterilization, batching (media/buffer), column chromatography, filtration and recording/collecting experiment data. Ability to work independently with ability to support complex troubleshooting, training and flexing in 2 work areas / operating systems Collaborate and interact with customer groups and suppliers on routine basis Participate as a team member on functional, organizational and cross functional teams Assist in maintaining an organized, safe, and clean work environment Coordinate and perform operations and tasks associated with CHO Drug Substance and Drug Product Operations Complies with all Plant safety and training guidelines Equipment maintenance and purchase Gives speaker presentations within work group BA/BS in a life science preferred or equivalent biologics work experience At least 1 year of Biologics experience with Purification experience preferred Demonstrates proficiency in the application of basic manufacturing, engineering and/or scientific theories, principles and techniques used in biopharmaceutical manufacturing processes Ability to work in fast paced dynamic work environment Ability to keep clear and accurate written and electronic records of work Strong team player who can work with team of diverse skills and objectives Ability to lead teams or projects that are assigned Possess excellent interpersonal and communication skills Strong problem solving skills Self-motivated, organized and capable of prioritizing deliverables across multiple projects Mechanical aptitude and ability to lift 30 pound", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null, "canonicalPositionUrl": "https://magnitdirectsourcing-rch.magnitglobal.com/careers/job/137458412022", "isPrivate": false}, {"id": 137458335114, "name": "Environmental Health and Safety Specialist", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1701207536, "t_create": 1701207390, "ats_job_id": 137458335114, "display_job_id": 137458335114, "type": "ATS", "id_locale": "137458335114-en", "job_description": "\u25cf Executes tasks in support of EHS programs with general direction and guidance from the EHS AD or EHS supervisor, program managers and business partners. The work may include: inspections, assessments, program audits, incident investigations, data reporting, monitoring and report submissions. \u25cf Supports daily EHS client needs alongside program managers and business partners, including: responding to inquiries from clients, participating in meetings and assisting with incident investigations and corrective & preventive actions (CAPAs). \u25cf Conducts EHS program compliance assurance audits, including data collection, employee interviews and area walkthroughs. \u25cf Supports EHS program managers and business partners in their effort to proactively identify opportunities and solutions to improve EHS programs. \u25cf Assists with the development and delivery of EHS training. Works with EHS program managers to improve training materials and effectiveness. \u25cf Participates in some regulatory inspections and internal/external audits. \u25cf Maintains applicable safety and environmental permits and permit conditions. \u25cf Supports engagement and communications with clients and EHS staff regarding EHS activities and performance. \u25cf Responds to client inquiries and requests with a high sense of urgency. \u25cf Assists with project prioritization and promotion of a proactive EHS culture, leveraging knowledge built of EHS business processes. \u25cf Participates and supports business process improvement activity as a team member, contributing to a proactive EHS culture. Identifies opportunities from challenges. Champions EHS with key stakeholders. \u25cf Serves as needed as a Safety Officer during disaster/emergency response and recovery efforts. May also be required to serve as EHS Advisor (technical expert) for the emergency response team during company-related emergencies. \u25cf Experience with practical application of safety, environmental (i.e, OSHA, EPA, DOT, NIOSH, etc.) and other regulatory requirements applicable to GMP and non-GMP environments. \u25cf Works well in a fast-paced environment and makes sound EHS decisions with some oversight and direction. \u25cf Effective communicator in both verbal and written formats; comfortable with leading meetings, delivering training and developing written communications. \u25cf Responsive to client and other stakeholder inquiries and requests with a high sense of urgency. \u25cf Proactive in their approach to finding opportunities and solutions for EHS program implementation and improvement. \u25cf Demonstrates the ability to support multiple program managers and business partners simultaneously, while staying organized and focused. \u25cf Education: BA or BS in occupational safety, environmental/health sciences or related field, or equivalent work experience \u25cf Minimum of 2-7 years of relevant experience, preferably in pharmaceutical, biotech, medical device or high tech industries \u25cf Knowledge of hazardous waste regulations and biosafety \u25cf Proficient with Microsoft Word, Excel, and Powerpoint as well as the Google suite of programs (gMail, gCal, docs, sheets, slides, etc.) \u25cf This position is not eligible for relocation. This is the pay range that Magnit reasonably expects to pay for this position: $30.64/hour-$40.86/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. If you have a disability and need an accommodation in relation to the online application process, please email us at Roche.Accommodations@magnitglobal.com", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null, "canonicalPositionUrl": "https://magnitdirectsourcing-rch.magnitglobal.com/careers/job/137458335114", "isPrivate": false}, {"id": 137458323165, "name": "Research Associate III", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1701114532, "t_create": 1701113838, "ats_job_id": 137458323165, "display_job_id": 137458323165, "type": "ATS", "id_locale": "137458323165-en", "job_description": "Job Description: BioAnalytical Sciences Operations translates and applies strategy and innovation for bioanalysis and immunogenicity into clinical and non-clinical studies through global collaboration and robust CRO portfolio management. Our team brings technical and operational expertise along with passion and drive to make a difference for patients. The Scientist 3 will support the development portfolio by providing technical oversight of clinical and non-clinical bioanalytical methods including validation and lifecycle management of Ligand Binding Assays supporting pharmacokinetic, toxicokinetic, pharmacodynamic, and biomarker analyses outsourced to Contract Research Organizations (CRO). The Scientist 3 will also review bioanalytical clinical and non-clinical method performance data generated at the CROs. The Scientist 3 will support the Genentech portfolio by: Serving as the front-line technical contact with CROs for routine outsourcing activities in support of method qualifications and validations (Ligand Binding Assays and new technologies) and any technical questions that arise around assay performance or lifecycle management during the course of clinical, non-clinical study assay performance. Providing technical oversight of outsourced methods (Ligand Binding and new technologies), ensuring qualified/validated state for optimal assay quality: Technical review of assay data from development, feasibility, qualification/validation, assay performance from clinical/non-clinical sample analysis. Technical review plans (qualification/validation/sample analysis), reports (qualification/validation/sample analysis) Technical support during assay troubleshooting and lifecycle management Proprietary Critical Reagents (Reference standards, MAbs, ligands): forecasting, requesting new material, shipping, re-test date extension. Supplemental validations to support additional matrices, disease states, co-medications, critical reagent incorporation, Coordinate assay transfers to multiple CROs and subsequent Technical support of cross validation experiments between CROs. Generate internal technical reports: validation history, cross validation, or memorandum Share with internal key stakeholders assay data (transfer, feasibility, qualification, validation, troubleshooting, assay performance) and documents (methods, plans, reports, memorandum). May Lead technical teleconferences with CROs and attend internal bioanalytical working group meetings. This individual will work in a fast-paced and highly collaborative team based environment. S/he will be asked to present at bioanalytical working groups or all staff meetings and to prepare poster presentations. S/he may train others on group responsibilities and systems. S/he may also be responsible for implementation or maintenance of support systems and may lead department teams charged with improving business processes. Qualifications: Bachelor's or Master's degree in Bioanalytical Sciences, Analytical Chemistry, Biochemistry or equivalent experience 3-8 years in industry and/or testing laboratory (Clinical, non-clinical, or CRO). Familiarity with bioanalytical method GxP compliance is required. The Scientist 2 or 3 may have a technical background in developing, validating, implementing, maintaining, and troubleshooting quantitative assays as well as have demonstrated problem solving abilities of bioanalytical methods in: LC-MS This is the pay range that Magnit reasonably expects to pay for this position: $45.00/hour-$61.24/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. If you have a disability and need an accommodation in relation to the online application process, please email us at Roche.Accommodations@magnitglobal.com", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null, "canonicalPositionUrl": "https://magnitdirectsourcing-rch.magnitglobal.com/careers/job/137458323165", "isPrivate": false}, {"id": 137458222113, "name": "Business Process Analyst", "location": "Oceanside, CA", "locations": ["Oceanside, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1700526706, "t_create": 1700525672, "ats_job_id": 137458222113, "display_job_id": 137458222113, "type": "ATS", "id_locale": "137458222113-en", "job_description": "Gain high level view of customer service process ecosystem and build process map including various streams Identify key data sources, inclusive of SNOW, Community of Practice track and trends data and relevant IT tickets. Analysis of data to drive identification of key opportunities for improving process performance. Identify areas for improvements and prioritize a working list Provide analysis documenting key failure modes and opportunities for improvement. Work with Internal Customers, Training Team and Network Support Groups to update current processes with improvements. Support organizational change management Assist Training Team with incoming Customer Service data flows Disseminate information regarding tools, reports, or metadata enhancements. Synthesize current business intelligence or trend data to support recommendations for action. Communicate with customers, stakeholders, internal vendors on progress and identified opportunities. Document specifications for business intelligence or information technology (IT) reports, dashboards, or other outputs. Create business intelligence tools or systems, including design of related databases, spreadsheets, or outputs. Generate standard or custom reports summarizing business, financial, or economic data for review by executives, managers, clients, and other stakeholders. Undergraduate degree preferred Computer Science/Management Information Systems or related field desired Strong background in business process analysis Experience with ServiceNow Experience with business intelligence systems Smartsheets experience would be a plus Onsite in Oceanside", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null, "canonicalPositionUrl": "https://magnitdirectsourcing-rch.magnitglobal.com/careers/job/137458222113", "isPrivate": false}, {"id": 137458222097, "name": "Research Associate I", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1700525576, "t_create": 1700525161, "ats_job_id": 137458222097, "display_job_id": 137458222097, "type": "ATS", "id_locale": "137458222097-en", "job_description": "The candidate must have 6 months to 1 year prior research lab experience (lab coursework does not apply) and must be proficient in molecular biology techniques (pipetting, dilutions etc ) and be highly flexible to handle urgent project-based requests, and to perform multiple laboratory duties. Strong organizational, communication, and interpersonal skills. Team oriented and dependable. Ability to follow detailed verbal and written instruction. Experience with tissue culture and molecular biology necessary. The candidate will be expected to have proficiency with general cellular biological and biochemical techniques. Must be self-motivated, able to multi-task, and meet timelines efficiently and productively. Strong verbal communication, writing, and listening skills, as well as interpersonal skills required. Excellent skills in communication, organization, flexibility and an eagerness to learn. Must be highly motivated team player and work well with others. This position is ideal for a candidate looking to apply to a PhD program in 1-2 years and needs experience in a cutting edge research environment. BS/BA in Genetics, Microbiology, Cellular and Molecular Biology, or related field. Specific skills include: mouse handling and dissection, and cellular biology, biochemical and standard laboratory techniques. Familiar with MS Word, Excel, and PowerPoint. Able to keep data accurately, as well as read, comprehend, and discuss research materials. 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