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Works from schematics, diagrams, written and verbal descriptions, layouts or defined plans to perform testing, checkout and trouble-shooting functions. Adheres to Roche Tissue Diagnostics procedures and processes. Makes plans, executes and revises as needed to accomplish assigned tasks to meet expectations of quality and time. Works as an effective departmental or cross-functional team member within a matrix organization. Monitors work to ensure quality, and continuously promote Quality First Time. Must be able to work proficiently in regard general IT/networking and security concepts Other duties as assigned by management. Bachelor's Degree or equivalent in a directly related discipline or equivalent combination of education and experience. Three years related experience in hardware/software troubleshooting and support. Entry Level. Demonstrates potential for technical proficiency, engineering creativity, collaboration with others and independent thought. Knows basic and some specialized engineering techniques Familiar with searching technical literature. Basic knowledge of hardware (PC) imaging software to ensure software laboratory can be configured in a repeatable manner Working knowledge of Virtual Machine setup and configuration Skilled with use of word processing, spreadsheets, graphical and presentation software applications Learns company and industry design practices as applied to tasks. Learns company practices for SW integration and test. 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Organize software training materials and maintain active communication with users Maintaining instruments by adhering to weekly and monthly routine maintenance procedures Communicating and escalating issues to stakeholders or the MS walkup core lead when appropriate Collaborating with the MS walkup core lead on improving and maintaining current walkup core practices in line with operational excellence", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://magnitdirectsourcing-rch.magnitglobal.com/careers/job/137459536301", "isPrivate": false}, {"id": 137459472463, "name": "Software/Data Engineer", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1706821686, "t_create": 1706821449, "ats_job_id": 137459472463, "display_job_id": 137459472463, "type": "ATS", "id_locale": "137459472463-en", "job_description": "Knowledge of Windows and Linux computer systems 5-7 years of development experience and experience with Python, Javascript, JQuery Familiarity with database technologies (e.g., SQL, NoSQL) Experience working with current web-based technologies and infrastructure Experience with reporting visualization tools such as Tableau, SEEQ Bachelor's degree in Computer Science, Software Engineering, or a related field (or equivalent experience). Excellent communication and teamwork abilities Self-motivated with the ability to explore innovative technologies to consistently achieve desired results Strong problem-solving skills and attention to detail Self-starter who actively takes initiative to correct issues with systems An understanding of biopharmaceutical process manufacturing practices Experience working with GxP validated systems Experience with information management systems, data historians, business intelligence, or data warehousing tools Familiarity with batch manufacturing automation controls (e.g. RSBatch) LowCode/NoCode tools such as Tulip Interfaces, Quickbase, etc. Experience with cloud platforms (e.g., AWS, Azure, Google Cloud) Experience with data modeling, ETL processes, and data warehousing.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://magnitdirectsourcing-rch.magnitglobal.com/careers/job/137459472463", "isPrivate": false}, {"id": 137459468536, "name": "Specialist Site IT, Associate", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1706805071, "t_create": 1706804782, "ats_job_id": 137459468536, "display_job_id": 137459468536, "type": "ATS", "id_locale": "137459468536-en", "job_description": "Supports and maintains effective relationships with users. Provides and documents day-to-day technical support to employees for internal desktop systems software, hardware, data, voice, and related peripherals. Installs, configures, and troubleshoots desktop systems/workstations, peripherals, voice/mobile devices, and network issues. Maintains passwords, data integrity and file system security for the IT environment. Organizes and follows complex and/or detailed technical procedures. Consults with clients to resolve technical problems and ensure customer satisfaction. Provides courteous and timely customer service, tracks inventory of IT assets. Knowledge of Windows operating systems, client/server environments within a corporate network structure, fundamental networking concepts, and troubleshooting methodologies. Knowledge of voice/mobile communication devices, technical skills for analyzing and problem-solving The ability to communicate effectively with a diverse team and work as a team player in a fast paced environment. 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Knowledge/Skills/Competencies Has full knowledge of the job and a general knowledge of related functions. Uses ability as a skilled specialist in accordance with company policies and procedures to complete complex assignments within defined parameters. Thorough knowledge of the fundamental operating principles of industrial process instrumentation and systems. Ability to distinguish colors. Ability to interpret electrical schematic diagrams; both IEC and NEMA. High School Diploma Experience (may vary depending on site size/scope) 12+ Years related experience 4 years in manufacturing process instrumentation and control and/or analytical instrumentation or a closely related job preferred. Experience with SAP and Blue Mountain RAM would be preferable. Assistance with systems start-up and validation. Troubleshooting and modification of process control instruments or systems, laboratory instruments and analyzers, and support utilities. Evaluate, and review Standard Operating Procedures content and red line where appropriate.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://magnitdirectsourcing-rch.magnitglobal.com/careers/job/137459399697", "isPrivate": false}, {"id": 137459399683, "name": "Scientist I", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1706714918, "t_create": 1706714607, "ats_job_id": 137459399683, "display_job_id": 137459399683, "type": "ATS", "id_locale": "137459399683-en", "job_description": "Description: We are seek a highly motivated contractor scientist to focus on analytical testing of samples from formulation development studies within the Genentech Pharmaceutical Development (PharmDev) Department, onsite in SSF. The successful candidate will work within a team tasked with conducting a range of analytical test procedures for molecules in our portfolio. The candidate will work in a core testing lab. This position requires effective participation in a team environment. Primary responsibilities will involve a broad range analytical testing methodologies for samples submitted to this lab. This role will require knowledge of analytical methods such as HPLC, CE, UV-Vis Spectroscopy, to name a few. Standard lab skills would be required. Evidence of strong verbal and organizational skills as well as attention to detail, are essential for this contractor position. The Candidate The qualified individual will possess a B.S. and possibly M.S. in a biological science, analytical chemistry, polymer chemistry, biomaterials or chemical engineering . Minimum of 1-3 years of relevant experience in academia, biotechnology and/or pharma. This is the pay range that Magnit reasonably expects to pay for this position: $35.00/hour-$55.91/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 Ref: 25232", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null, "canonicalPositionUrl": "https://magnitdirectsourcing-rch.magnitglobal.com/careers/job/137459399683", "isPrivate": false}, {"id": 137459399644, "name": "Research Associate II", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1706736667, "t_create": 1706713624, "ats_job_id": 137459399644, "display_job_id": 137459399644, "type": "ATS", "id_locale": "137459399644-en", "job_description": "Description: A good majority of their day will be spent working on operations type work. (formulations, cartridge/dispenser filling, labeling, kitting, etc) We require RA level people in our area because we do not have support teams beyond our group. Any documentation, troubleshooting, experimentations, protocol work will be done by this person as well. They should consider the Pilot Plant like a small, self contained, group. They will be asked to wear many different hats during the day so flexibility is key. Along with Lab/Production style work, they will be supporting the documentation for these projects (completing formulation/fill documents, creating shipping documentation for export projects, and obtaining documents (CofAs) from vendors). Attention to detail is important. This person will be working in the lab and at the computer each day to complete Reagents and supporting documents to ship internally and externally. They will be working with other team members and supporting the international teams on some projects. they will be communicating (live, email, shared drives) with these teams to ensure the projects are completed on time and right the first time. They should be able to support multiple projects, at different stages, and manage competing priorities. Education: Bachelors in a related field 2-4 years of experience This is the pay range that Magnit reasonably expects to pay for this position: $27.00/hour-$27.00/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. 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Executes and reports on validation studies such as Process Validation, Cleaning Validation, CSV, Commissioning, IQ, OQ and PQ studies. Resolve technical issues encountered during study execution. Track and expedite the review and sign-off of qualification documentation. Support execution of validation activities. Interact with individuals from different departments to plan, execute, and complete qualification activities. Drive the completion of validation efforts according to deadlines. Write / guide the writing of departmental procedures required for validation. Assist during internal and 3rd party audits wrt validation requirements. Initiate CAPAs, NCRs and Change Requests where required and assist with investigations. Assist with identifying maintenance and calibration requirements. Coordinate suppliers wrt Validation activities including obtaining quotes from suppliers. Validation administration such as updating the validation plan, maintaining databases, standard referencing of documentation. Review Validation plans, protocols and SOPs written by other validation team members. Manage workload arising from unscheduled events. 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. 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