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} .support-section { padding: 15px !important; } .join-section { padding: 15px !important; } .support-list-sec { flex-wrap: wrap; } .work-main { padding: 15px !important; } .active-sec { flex-wrap: wrap; } .active-sec div { width: 100% !important; max-width: 100% !important; } .active-sec div:first-of-type img { width: 100%; } .active-sec div:first-of-type { margin-bottom: 15px; } .active-sec div:last-child{padding-left: 20px;}.work-section h3, .work-section div h3:nth-child(2), .work-section div h3:nth-child(4) { position: relative !important; width: 100% !important; left: 0 !important; text-align: left !important; top: auto !important; } .work-section img { margin: 0 0 20px 0; }} @media screen and (max-width: 715px){.navbar img {height: 15px}} .support-list-sec div:nth-child(2n) { margin: 0 20px; } .active-sec img { width: -webkit-fill-available; } nav.navbar { position: absolute !important; } #myModal .modal-body { padding: 65px 100px; height: 600px; overflow-y: scroll; } #myModal .modal-content { margin: 60px 0 0 0; } #myModal .modal-header { padding: 0; border-bottom: none; } #myModal .modal-header .close { margin: -52px 0px 0 0; color: #fff; opacity: 1; font-size: 50px; font-weight: normal; } #myModal h1 { color:#000; font-weight: 700; font-size: 32px !important; padding-bottom: 40px; line-height: 40px; } #myModal h3 { color:#000; font-weight: 700; font-size: 28px !important; padding: 25px 0 25px;} #myModal ul{ padding-left: 22px; } #myModal ul li{ color:#000; font-size:22px; } div#myModal .modal-dialog { max-width: 980px; width: 100%; padding: 0 25px; margin: 0 auto; } div#myModal {z-index: 999999 !important;} .white-bttn:hover { background: #fff !important; color: #8d1f1b !important; } .black-button:hover { background: #000 !important; color: #fff !important; } .learn-more:hover img { margin: 0 0 0 15px !important; transition: linear .5s; -webkit-transition: linear .5s; } .btn.upload-resume-button {white-space: normal;}"}, "custom_html": {"page-footer": "<p className='body-text-2'><a title='Visit Eightfold.ai homepage' target='_blank' rel='noopener noreferrer' style={{ color: 'black' }}><img src='https://static.vscdn.net/images/pro_direct_source.svg' alt='' width='100' height='11' align='middle' style='margin-bottom: 3px'/> &thinsp; %(text)s PRO Unlimited & eightfold.ai</a> </p>", "page-footer-text": "powered By"}, "custom_head_scripts": {"HOME_PAGE_LOAD": "<script>var html = '<div class=\"custom_header_content\"><div class=\"modal\" id=\"myModal\"><div class=\"modal-dialog\"><div class=\"modal-content\"><div class=\"modal-header\"><button type=\"button\" class=\"close\" data-dismiss=\"modal\">&times;</button></div><div class=\"modal-body\"><h1> Why join the Novartis Talent Community of External Workers</h1><h3>Why it\u2019s great to be an external worker at Novartis</h3><ul><li> Learn about Novartis values</li><li>Learn about Novartis noble purpose</li><li>Learn about ongoing temporary projects at Novartis</li></ul><h3>Be the first to know about new temporary projects</h3><ul><li>Take part in one intake call so we understand your skills and professional goals</li><li>Whenever there are new projects that meet your skills, our PRO Unlimited Team will contact you immediately</li><li>You only give us approval to submit your profile and we manage the rest</li><li>Because our process is fast, you will always be on top of the candidate list</li></ul><h3>News in your inbox</h3><ul><li>Receive periodic updates about new developments at Novartis</li><li>Hear success stories on how temporary talent makes an impact</li><li>Receive business news in the marketplace that brings value to your professional growth</li></ul></div></div></div></div></div><div style=\"margin: 20px auto 40px; height: 44px;background: url(https://static.vscdn.net/images/careers/demo/directsourcepro-nov/1662987645::1658306546__bg-strip-pattern.png); \"></div> <div class=\"active-sec\" style=\"display: flex; margin-bottom: 100px; align-items: flex-start; justify-content: space-between;\"> <div style=\"max-width: 48%; overflow: hidden; width: 48%;\"><img src=\"https://static.vscdn.net/images/careers/demo/directsourcepro-nov/1662987974::1658307174__projects.jpeg\"></div><div style=\"max-width: 48%; overflow: hidden; width: 48%;\"><h3 style=\"font-weight: 700; font-size: 32px !important; padding-bottom: 50px; margin:0; padding-right: 60px; line-height: 40px;\">Active Projects for External Workers</h3><p style=\"margin-bottom: 25px; font-size: 16px; line-height: 22px;\">Novartis continuously looks to connect with people like you who want to apply their skills, knowledge and curiosity in a flexible, diverse and inclusive employee culture. Where you are unbossed to drive your own personal growth, share new ideas and where you are surrounded by colleagues who are equally determined to transform lives.</p><a id=\"view-novartis-projects-btn\" class=\"black-button\" style=\" font-weight: bold; font-size: 16px; background: transparent; border: solid 2px #221f1f; color:#221f1f; padding: 8px 10px; line-height: 40px; padding-left: 20px; padding-right: 20px;\">View Novartis Projects</a></div></div> <div class=\"join-section\" style=\"background: url(https://static.vscdn.net/images/careers/demo/directsourcepro-nov/1662987698::1658314245__bg-contractor-community.jpeg); background-size: cover; padding: 50px;\"><div style=\"max-width:720px; background: #8d1f1b; padding: 35px; color: #fff;\"><h3 style=\"font-size: 30px !important; margin: 0 0 40px 0; font-weight: 700;\">Why join the Novartis Talent Community of External Workers</h3><div class=\"support-list-sec\" style=\"display: flex; align-items:flex-start; justify-content: space-between;\"><div><p>Support the Novartis purpose to reimagine medicine for patients.</p><ul style=\"padding-left: 20px;\"><li style=\"margin-bottom: 15px;\">Novartis focuses on unleashing the power of their people</li><li style=\"margin-bottom: 15px;\">Novartis values diversity, a unique culture and supports an inclusive, unbossed environment</li></ul></div><div><p>Be the first to know about new temporary projects for external workers at Novartis.</p><ul style=\"padding-left: 20px;\"><li style=\"margin-bottom: 15px;\">The PRO Unlimited team will pro actively communicate opportunities that are a fit for you.</li></ul></div><div><p>News at your finger tips.</p><ul style=\"padding-left: 20px;\"><li style=\"margin-bottom: 15px;\">Receive regular updates about temporary projects at Novartis</li></ul></div></div><div><a data-toggle=\"modal\" data-target=\"#myModal\" class=\"learn-more\" style=\"color: #fff; font-weight: 700; padding: 10px 0; margin: 17px 0 0 0; display: inline-block;\" href=\"#\">Learn more <img style=\"display: inline-block; width: 18px; margin-left: 7px; padding: 0; transition: linear .5s; -webkit-transition: linear .5s;\" src=\"https://static.vscdn.net/images/careers/demo/directsourcepro-nov/1662987872::arrow-small-right-white.svg\"></a></div></div></div><div class=\"work-main\" style=\"padding: 100px 50px 180px;\"><h2 style=\"font-weight: 700; font-size: 32px !important; margin-bottom: 50px;\">How it works - It&#39;s simple</h2><div class=\"work-section\" style=\"position: relative;max-width: 1550px;margin:0 auto;\"><img style=\"width: 100%;\"src=\"https://static.vscdn.net/images/careers/demo/directsourcepro-nov/1662988697::works.png\"><div><h3 style=\"position: absolute; left: 10px; width: 140px; top: 150px; font-size: 18px !important; text-align: center; font-weight: bold; line-height: 23px;\">Join the Community</h3><h3 style=\"position: absolute; left: 31%; width: 140px; top: 300px; font-size: 18px !important; text-align: center; font-weight: bold; line-height: 23px;\">Answer a few questions so we get to know you</h3><h3 style=\"position: absolute; left: 62%; width: 140px; top: 165px; font-size: 18px !important; text-align: center; font-weight: bold; line-height: 23px;\">Pro Unlimited will match your expertise to temporary projects</h3><h3 style=\"position: absolute; left: 91%; width: 140px; top: 290px; font-size: 18px !important; text-align: center; font-weight: bold; line-height: 23px;\">We will submit you to active projects</h3></div></div></div><div class=\"support-section\" style=\"background: url(https://static.vscdn.net/images/careers/demo/directsourcepro-nov/1662987741::1658323457__bg-novartis.jpeg); background-size: cover; padding: 140px 50px;\"><div style=\"max-width:650px; background: #8d1f1b; padding: 35px; color: #fff;\"><h3 style=\"font-size: 30px !important; margin: 0 0 40px 0; font-weight: 700;\">Why support Novartis Projects</h3><div style=\"display: flex; align-items:flex-start; justify-content: space-between;\"><div><ul style=\"padding-left: 20px;\"><li style=\"margin-bottom: 15px;\">You want to support a team that believes in innovation, quality, courage and integrity</li><li style=\"margin-bottom: 15px;\">Your expertise could help impact patient outcomes</li><li style=\"margin-bottom: 15px;\">You will experience a collaborative culture</li><li style=\"margin-bottom: 15px;\">Novartis temporary projects may support your professional growth</li><li style=\"margin-bottom: 15px;\">Flexible work or service arrangements whenever possible</li><li style=\"margin-bottom: 15px;\">Competitive rates</li></ul></div></div><div><a id=\"nov-join-now\" class=\"white-bttn\" style=\"color: #fff; font-weight: 700; padding: 10px 20px; border: solid 2px #fff; margin: 17px 0 0 0; display: inline-block;\">Join Now!</a></div></div></div></div></div>';$(\"#EFSmartApplyContainer .header-wrapper\").append(html);\n$(\"#view-novartis-projects-btn\").click(function(){\n $(\"html,body\").animate({scrollTop: $(\"#pcs-body-container\").offset().top},\"slow\");\n});\nvar join_talent_link = $('.join-tn-link').attr('href');\n$('#nov-join-now').attr('href', join_talent_link)\n</script>"}, "recaptcha_enabled": 0}, "positions": [{"id": 171812222328, "name": "Executive Assistant Administration", "location": "East hanover", "locations": ["East hanover", "East Hanover, NJ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663899602, "t_create": 1663899510, "ats_job_id": 171812222328, "display_job_id": 171812222328, "type": "ATS", "job_description": "Click here to learn more about Magnit (hyperlink to your website) Ready to work with/through Magnit at Novartis? Requirements: Person will act as Administrative Assistant for 3 senior members in Procurement (All based in EH with global teams). Work closely with Senior Executive Admin and provide backup as needed Provide logistical support for workshops, large/small meeting Expert Cross Cultural Experience Collaborating across boundaries Continuous improvement of processes and procedures Planning of the office needs and management of contracts with all contractor General administrative support: takes care of general administrative tasks and maintains the administrative processes also in case of absence of the line manager/team members. Interaction: Informs, advises and supports the team and associates from outside the team on processes, guidelines and services that are specific to the department. Work processes in own area of responsibility Supports optimization of current processes and/or introduction of new or modified processes. Handling of administrative projects tasks with clearly defined content and time limitations. Acts as a team member for administrative projects and manages the administrative part of special tasks. Supervisory tasks: Guarantees a smooth adjustment to the job of new employees in the own area of responsibility. Takes over supervising for colleagues in the administrative area (e.g. apprentices, new employees etc.) Plan and coordinate administrative procedures and systems and devise ways to streamline processes. Responsible for the independent delivery of profound administrative services in a local and a global context. Ensure service levels are delivered in line with site requirements. Requirements: Digital & Technology Savvy Operational Excellence Organizational Savvy Managing Change Continuous Learning (Dyn. Knowledge Development) Project Excellence Being resilient Managing Diversity Effective Communication Proactive thinking Franchise Strategy Prioritization Timely decision making Knowledge of organization structures and working practices Best practice sharing MUST have experience with Outlook, MS Team, travel, be quick to respond, detail oriented and a hard worker! Word, Outlook, Excel, PowerPoint, and SharePoint, Microsoft Team Strong interpersonal skill Organized and ability to work under timelines Education: HR Diploma required Why Novartis? Accommodation:", "stars": 0.0, "medallionProgram": null}, {"id": 171812194148, "name": "Quality Control Analyst", "location": "East Hanover, NJ", "locations": ["East Hanover, NJ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": null, "t_create": 1663785829, "ats_job_id": 171812194148, "display_job_id": 171812194148, "type": "ATS", "job_description": "Summary: In this individual contributor role, the Quality Control Analyst will support patient throughput and compliance activities within the Quality department. Responsibilities: Execute in-process and release testing on batches including, but not limited to, flow cytometry, IFNg potency, qPCR, cell count and viability, sterility, and endotoxin. Perform data review, generate Certificates of Analyses for release of final produce in accordance with company procedure Work with cross-functional stakeholders to meet company timelines Helps maintain progress of projects Ensures that all planned, executed, and documented activities are aligned with company and site objectives. Ensures adherence to all company policies and procedures relating to current Good Manufacturing Practices, Standard Operating Procedures and Health, Safety and Environmental Protection regulations. Assists Quality Control, AS&T, and Quality Assurance in investigations of assay-related issues. Provides timely response to requests for support of manufacturing deviations, investigations and change requests. Performs or supports other tasks related to Quality and site operations, as needed Shift: SUN - WED, 1430 - 0030 Requirements: Experience with cytometry Experience with cell count and viability Bachelor's degree preferred Why Novartis? Accommodation:", "stars": 0.0, "medallionProgram": null}, {"id": 171812194147, "name": "Quality Control Analyst", "location": "East Hanover, NJ", "locations": ["East Hanover, NJ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": null, "t_create": 1663785764, "ats_job_id": 171812194147, "display_job_id": 171812194147, "type": "ATS", "job_description": "Summary: In this individual contributor role, the Quality Control Analyst will support patient throughput and compliance activities within the Quality department. Responsibilities: Execute in-process and release testing on batches including, but not limited to, flow cytometry, IFNg potency, qPCR, cell count and viability, sterility, and endotoxin. Perform data review, generate Certificates of Analyses for release of final produce in accordance with company procedure Work with cross-functional stakeholders to meet company timelines Helps maintain progress of projects Ensures that all planned, executed, and documented activities are aligned with company and site objectives. Ensures adherence to all company policies and procedures relating to current Good Manufacturing Practices, Standard Operating Procedures and Health, Safety and Environmental Protection regulations. Assists Quality Control, AS&T, and Quality Assurance in investigations of assay-related issues. Provides timely response to requests for support of manufacturing deviations, investigations and change requests. Performs or supports other tasks related to Quality and site operations, as needed Shift: WED - SAT, 0800 - 1700 Requirements: Experience with cytometry Experience with cell count and viability Bachelor's degree preferred Why Novartis? Accommodation:", "stars": 0.0, "medallionProgram": null}, {"id": 171812193863, "name": "Quality Control Analyst", "location": "East Hanover, NJ", "locations": ["East Hanover, NJ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663785560, "t_create": 1663785461, "ats_job_id": 171812193863, "display_job_id": 171812193863, "type": "ATS", "job_description": "Summary: In this individual contributor role, the Quality Control Analyst will support patient throughput and compliance activities within the Quality department. Responsibilities: Execute in-process and release testing on batches including, but not limited to, flow cytometry, IFNg potency, qPCR, cell count and viability, sterility, and endotoxin. Perform data review, generate Certificates of Analyses for release of final produce in accordance with company procedure Work with cross-functional stakeholders to meet company timelines Helps maintain progress of projects Ensures that all planned, executed, and documented activities are aligned with company and site objectives. Ensures adherence to all company policies and procedures relating to current Good Manufacturing Practices, Standard Operating Procedures and Health, Safety and Environmental Protection regulations. Assists Quality Control, AS&T, and Quality Assurance in investigations of assay-related issues. Provides timely response to requests for support of manufacturing deviations, investigations and change requests. Performs or supports other tasks related to Quality and site operations, as needed Shift: WED - SAT, 1430 - 0030 Requirements: Experience with cytometry Experience with cell count and viability Bachelor's degree preferred Why Novartis? Accommodation:", "stars": 0.0, "medallionProgram": null}, {"id": 171812193206, "name": "Document Management Resource", "location": "East Hanover, NJ", "locations": ["East Hanover, NJ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663783793, "t_create": 1663783551, "ats_job_id": 171812193206, "display_job_id": 171812193206, "type": "ATS", "job_description": "Responsibilities: Development of content for Working Practice Documents (WPDs) and Work Instructions (WIs) Translating process maps into easy to follow, step-by-step executable instructions Ability to translate instructions into pre-defined templates with required content Closely interfacing with various stakeholders and business partners to ensure content accuracy, thoroughness, and design of various documents. Light project management for documents being created, including status'/progress tracking and timeline management Responsible for coordination of the full document approval process, from draft reviews to final approvals Requirements: Fluent in English Consistently detail oriented High-level proficiency in Microsoft Word and Adobe Acrobat. Experience in Vizio is a plus Experience in Word processing and editing documents including use of templates, standardized formatting, and visual aids Previous Technical Writing and/or Document Control experience, preferably in a GxP environment Why Novartis? Accommodation:", "stars": 0.0, "medallionProgram": null}, {"id": 171812105934, "name": "QC Chemist", "location": "Wilson, NC", "locations": ["Wilson, NC"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663281912, "t_create": 1663281869, "ats_job_id": 171812105934, "display_job_id": 171812105934, "type": "ATS", "job_description": "Description: Quality Control Technician, Lab Technician, Associate Scientist, Microbiologist, QC Microbiology Analyst Sound technical and scientific understanding; experience in pharmaceutical or chemical analytics/QC or equivalent Preferred: Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production), aseptic technique. Orders are processed correctly and quickly no waiting times due to wrong or delayed order. Deadline adherence rate: orders completed on time, all missed deadlines reported in good time, the shortest possible lead time. Ensure constant readiness for inspection, no critical complaints from superiors and inspectors. Consistently follow the GMP and GSU guidelines, as well as the SOPs, no critical irregularities. Finding and implementing optimization options to reduce costs Completed training plan. Sample storage and management Analytical testing/documentation of drug product / finished product / complaints / stability / packaging material samples to GxP standards. Stability Testing/Sample storage and management Analytical documentation of stability samples to GxP standards. This role utilizes chemistry laboratory skills to test and measure product or materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods, and current Compendia. Administrative activities and GMP and HSE-compliant. Quality Control Sampling knowledge of TQM and related industry GxP standards and processes. Laboratory Excellence Quality decision making Infrastructure Management Why Novartis? Accommodation:", "stars": 0.0, "medallionProgram": null}, {"id": 171812105542, "name": "Medical Associate", "location": "Princeton, Nj", "locations": ["Princeton, Nj"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663280506, "t_create": 1663280393, "ats_job_id": 171812105542, "display_job_id": 171812105542, "type": "ATS", "job_description": "Description: In collaboration with the PMEE Operations Manager/Associate Director, the PMEE Operations Coordinator will provide operations support for all US PMEE material (promotional and non-promotional) approval process (MAP) related initiatives, with a key responsibility in FUSE Operations, support of non-promotional medical material review process, tagging and linking references for asset submission within the MAP platform and support other Operations activities related to SharePoint and/or Dashboard like technology-related PMEE services, congress planning and other PMEE deliverables. Ensure timely and high-quality operational support for all assigned PMEE deliverables, including: Support the AD/Manager, PMEE Operations in coordination of overall non-promotional materials review process for the entire Sandoz portfolio Coordinate the Material Approval Process, providing guidance to Asset Owners on process and strategic guidance to ensure quality and efficiency Assist with triaging all submitted assets by strategically assessing the asset content and determining the full or modified review path to Medical Legal and Regulatory (MLR) (Legal only, or Legal and Medical only etc.) Responsible for the day-to-day support of the MLR and associated cross-divisional process by serving as key contact for Asset owners and Agencies, as well as Reviewers from concept review requests to guide them through project initiation for delivery of final asset Ensure quality and consistency for all submitted non-promotional materials by supporting Live reviews and other MAP processes to ensure timely review Help PMEE Asset Owners with tagging and linking of references for asset submission within the MAP platform Proactively, support MLR Reviewers in prioritization of assets during high volumes, or to manage expedited reviews of materials Stay engaged with cross-divisional MAP Operations, including Help Desk or Training type support and resolve day-to-day system issues (outages, user access issues, etc. Monitor Re-Review Reports to ensure timely completion and compliance requirements Pull FUSE reports to assist with project tracking and quarterly reporting needs Proactive follow-up to ensure task completion within defined durations Ensure close collaboration with US PMEE Operations Managers/ Associate Director as well as cross-divisional Operations teams to identify synergies and harmonize processes, build best practices, along with periodic review of MAP Operations processes to identify areas for improvement Ensures compliance to Sandoz/Novartis and other relevant regulations and quality standards, shares best practices and lessons learned. Successful professional with 2-4 years of Project/Program management/Medical Affairs Operations experience and some material approval process experience Experience having effective interactions with appropriate levels of the organization and with an external audience Learning Agility Ability to prioritize, stay organized and meet deadlines under pressure or time constraints and to manage multiple projects in a fast-paced environment Ability to balance excellent customer service skills with strict compliance requirements Ability to collaborate across different functional areas to ensure alignment with governance processes and to meet business objectives is required Interpersonal, and communication skills are required Hybrid role Prefer local candidates so that the selected candidate can come into the office occasionally, about once every 6 weeks for team meetings Why Novartis? Accommodation:", "stars": 0.0, "medallionProgram": null}, {"id": 171812105232, "name": "Finance Associate", "location": "East Hanover, NJ", "locations": ["East Hanover, NJ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663277784, "t_create": 1663277700, "ats_job_id": 171812105232, "display_job_id": 171812105232, "type": "ATS", "job_description": "Description: Prepare Finance Core documentation inventory (Guidelines, Standard Operating Procedure (SOP), step outs, Local Supplemental Information (LSIs), Working Instructions (WIs), both global and local) Analyses Finance Core processes End to End (E2E) and perform gap analysis (step out) between AAA and GTx vs Novartis Finance Core List process gaps (step out) by business, process, system, organization and missing documentation (LSIs, global and local WIs) Identify new or changes to Novartis Financial Controls Manual (NFCM) controls embedded in processes and requirements for implementation Identify permanent step outs with clear and proper justification As part of the gap analysis find opportunities of improvements through standardization, automation and simplification Liaison/coordination with Global Process Owners/Global Standard Process Leads (GPOs/GSPLs), Financial Controls & Compliance (FC&C), Information Technology (IT) Identify and coordinate training requirements for new and/or adapted processes Coordinate and support the creation of WIs Regular project milestones reporting to Leadership Team The business is looking for 2 individuals with at least 1-2 years Finance Pharma experience and 1 Lead who may have more experience. This position will be a Hybrid model and working EST hours. 5+ years finance experience including FRA, auditing, internal controls and/or business process re-engineering Prior finance operational experience with practical knowledge of relevant processes and international exposure Desirable Strong project and change leadership skills Operating knowledge of D365, SAP or other ERP systems Good communication skills, proactivity, self-initiative Education: Bachelor's Degree in business, finance or Certified Public Accountant (CPA)/Chartered Accountant Why Novartis? Accommodation:", "stars": 0.0, "medallionProgram": null}, {"id": 171812095308, "name": "QA Expert Operations", "location": "San Diego, CA", "locations": ["San Diego, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663209525, "t_create": 1663209434, "ats_job_id": 171812095308, "display_job_id": 171812095308, "type": "ATS", "job_description": "Description: Quality Assurance Analyst, Quality Assurance Junior Specialist, Laboratory Supervisor/Assistant, Quality Assurance Associate/Assistant Experience in pharmaceutical quality control- quality assurance or production Operations Management and Execution Functional Breadth Collaborating across boundaries Applied Practice Customer satisfaction Punctuality rate Jobs done on time, following the specified cycle time Consistent compliance with GMP and Health, Safety and Environment guidelines and Standard Operating Procedures No complaints with regulatory inspections Maintains applicable Standard Operating Procedures (SOPs), GxP compliant documentation and records within the Novartis Quality Management System. Ensures the integrity of all Quality Systems records and data, as applicable and collaboration of own team with other functions and departments Ensures an adequate level of education, GxP knowledge Updates & maintains relevant information in electronic systems (e.g.Change Control, Documentation, Training Follow up and monitoring of e.g.CAPAs, actions, metrics Supports Quality Audits and Health Authority inspections Supports all GxP activities in the Quality department. Administers Quality Systems/ Processes including documentation, metrics and monitoring of actions. Supports establishment of Quality operational processes. Performs routine GxP Compliance/ Operational activities according to Novartis Quality Standards. Supports Quality Projects and initiatives. Continuous Learning (Dyn. Knowledge Development) Operational Excellence Digital & Technology Savvy Quality Assurance Knowledge of GMP Quality Standards Quality Control (QC) Testing Knowledge of IT Applications & tools knowledge of GMP Why Novartis? Accommodation:", "stars": 0.0, "medallionProgram": null}, {"id": 171812082142, "name": "Lab Technician - Chemistry", "location": "Cambridge, Massachusetts", "locations": ["Cambridge, Massachusetts"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1663108149, "t_create": 1663107727, "ats_job_id": 171812082142, "display_job_id": 171812082142, "type": "ATS", "job_description": "Description: The Sample Management group is looking for a highly motivated individual to be a key contributor within our team. As a member of the Sample Management group, the successful candidate will be primarily working within the Compound Hub, processing new Novartis compounds and inventory requests through the Compound Hub Process Key Functions: Primary responsibility will be handling of all new compound orders, weighing solid samples within a weigh hood using an analytical balance in order to create solutions, which then move onto the v Tecan Liquid Handler. Sample logistics including packaging and unpackaging samples from both internal and external locations. Responsible to ensure all service level agreements are achieved on a daily basis and to work with scientific staff directly to complete orders. Skills: A Bachelor's degree with experience working in a scientific lab, having an emphasis on compound inventory management and distribution utilizing automated systems Should have a thorough knowledge of activities related to compound management, including inventory management, solution production, quality control and logistics management Experience working with laboratory robotics Ability to diagnose and triage hardware and software issues quickly Good personal and communication skills. Ability to work well within a team Ability to multitask in a fast paced environment Must understand customer focus, and be professional in the work place Must be self-motivated, well organized, reliable and able to prioritize workload Working knowledge of MS Office products Desired Traits & Experience: This is a service orientated position requiring attention to detail, ability to work as part of a team and interact routinely with the scientific staff. Knowledge of some or all of the following instruments/systems are required: Tecan evo, Biomicrolab Volume Checker, Biomicrolab Tube Sorter 0-12 months of experience A Bachelor's degree with experience working in a scientific lab, having an emphasis on compound inventory management and distribution utilizing automated systems Why Novartis? 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