Contractor Positions at Novartis

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} #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": "<b>Magnit Direct Sourcing</b> powered by Magnit Global & 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 Magnit Global 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 Magnit Global 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;\">Magnit Global 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": 171815122148, "name": "Project Manager II", "location": "remote", "locations": ["remote", "United States"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1685634709, "t_create": 1685634661, "ats_job_id": 171815122148, "display_job_id": 171815122148, "type": "ATS", "id_locale": "171815122148-en", "job_description": "Serve as Project Manager to lead the successful delivery of the assigned project in a dynamic environment that embraces change Manage the project lifecycle according to the NOX project management approach while meeting all governance requirements Results-focus and passion for disciplined delivery Focuses on people over process and outcomes over artifacts Understands and effectively uses different project management approaches Understands adaptive and agile project management concepts and has a record of successfully applying the approaches in project delivery Has strong communication, team building, influencing and collaboration skills at all levels Successfully anticipates, mitigates, and resolves risks and conflict, escalating promptly when necessary Basic leadership skills and demonstrated ability to motivate a global, intra-discipline project team Uses collaboration-style decision making Effectively uses project management tools to facilitate decision making and enhance communication, and has a proactive approach to project delivery Demonstrated ability to successfully work with vendors University Degree 5+ years of experience in a project delivery role accountable for business outcomes 2+ years managing database-related projects in a technical environment Experience with use of agile and adaptive project management approaches Experience leading project teams of technical, scientific and business associates Experience implementing scientific applications in the pharmaceuticals industry", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 171815122106, "name": "Engineering Specialist", "location": "San Diego, CA", "locations": ["San Diego, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1685634164, "t_create": 1685634101, "ats_job_id": 171815122106, "display_job_id": 171815122106, "type": "ATS", "id_locale": "171815122106-en", "job_description": "Provides engineering, validation and maintenance support to the decommissioning of QC equipment, facility and utilities at a site; equipment may include lab equipment such as cellometers, CX5, Densitometers, support systems such as SCADA, incubators, freezers bio-safety cabinets, offline bench-top instruments or facility/utility systems. Ensures equipment is decommissioned in a compliant manner through equipment life cycle. Owns and manages changes to the lab equipment to maintain equipment in a validated state. Investigates any equipment or process deviations and developing corrective actions to prevent re-occurrences. Able to provide industry wide expertise for complex equipment and process investigations. Applies knowledge of engineering principles and best practices to ensure robust solutions. B.S. degree in Chemical, Electrical or Mechanical Engineering, or related technical field, with 5 years work experience in pharmaceutical or biopharmaceutical based GMP manufacturing operations, or equivalent work experience (9 years) in pharmaceutical or biopharmaceutical based GMP manufacturing operations. Strong technical writing ability required. Working in a team environment, with excellent communication and organizational skills. Diverse experience in the development, automation, and manufacture of gene therapy products, medical devices, instruments, or biotechnology. In-depth knowledge of FDA regulations and GMP systems and experience providing engineering support in a highly regulated or pharmaceutical / biotech facility. Strong project management skill set with extensive experience in strategic / tactical planning, demonstrated ability to perform long-term project planning. Ability to prepare contingency plans and logically work through complex issues in a pressure filled atmosphere. Demonstrated ability to lead cross functional teams across manufacturing locations in a fast pace, dynamic team setting. Uses professional concepts in accordance with company objectives to solve complex problems in creative and effective ways. Full understanding of area of specialization; resolves a wide range of issues in creative ways Ability to work on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 171814987748, "name": "Associate Global Trial Director", "location": "East Hanover, NJ", "locations": ["East Hanover, NJ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1684893401, "t_create": 1684893369, "ats_job_id": 171814987748, "display_job_id": 171814987748, "type": "ATS", "id_locale": "171814987748-en", "job_description": "Pay rate: Min 100/hr - Max 156.13 Health, Dental, Vision, 401k \uf0b7 \u22655 years of operational and managerial experience in planning, executing, reporting global clinical trials in a pharmaceutical company or a contract research organization. \uf0b7 Has guided, trained and/or developed direct reports. OR, has mentored and/or served as an onboarding partner in case of no prior people management experience. \uf0b7 Proven ability to work independently in a complex matrix environment (including remote or virtual team environment). \uf0b7 Strong project management skills and demonstrated ability to meet timelines. Strong interpersonal, problem solving and conflict resolution skills. \uf0b7 Experience in developing effective working relationships with internal and external stakeholders \uf0b7 Organizational awareness, including experience working cross-functionally and in global teams. \uf0b7 Proven record of managing resources (budget and headcount). Practice, clinical trial design and global drug development process. \uf0b7 Good knowledge of relevant therapeutic area(s) preferred. management of the assigned clinical trial(s) end-to-end to achieve Global Program Team (GPT), Global Clinical Team (GCT), CTT and GDO-TM objectives. Enables an empowered organization that can navigate in a matrix environment and adjust quickly to business needs. Builds best talent and an inspired, curious and empowered culture to foster high performance in a matrix environment. building, performance management and career development. Contributes to cross functional activities and functional initiatives, when appropriate. 4. Trial planning, execution and close-out: \uf0b7 Creates and/or drives trial level timelines. \uf0b7 Leads the CTT development of global clinical trial protocol(s), by translating the approved trial concept sheet(s) into efficient, high quality, executable clinical protocols, and trial related documents. \uf0b7 Oversees trial feasibility and facilitates development of global recruitment plan including contingencies in collaboration with Strategic Planning & Feasibility and Trial Monitoring organizations. \uf0b7 Oversees and contributes to the development of Case Report Forms (CRFs), edit checks, CRF completion guidelines, data quality plan and trial statistical analysis plan in collaboration with the trial data manager, trial statistician, statistical programmer and Clinical Development Representative(s). \uf0b7 Oversees activities including document submission to Health Authority and/or Institutional Review Board/Ethics Committee, drug supply forecast and management, and conducting investigator's meeting/training and other trial management and decision making, and proactive risk management. Builds support for ideas among stakeholders, negotiates effectively and makes management mindset in CTT.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 171814987651, "name": "Production Lead Support", "location": "millburn, NJ", "locations": ["millburn, NJ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1684892574, "t_create": 1684892465, "ats_job_id": 171814987651, "display_job_id": 171814987651, "type": "ATS", "id_locale": "171814987651-en", "job_description": "Prepare/modify the production activity schedule, according to the general production planning Organize shifts allocating people and equipment taking in to account all applicable HSE, GMP laws and other constraints Ensure all production activities are being performed compliantly Liaise with other departments, supply chain, QA, QC, engineering, for organizing production activities and to troubleshoot issues involving manufacturing Interact with production personnel for planning production and non-production activities such as training and addressing questions from operators Lead/facilitate weekly production meetings Perform other activities as assigned by the Production head/manager Operates in full compliance with GMP, HSE and other applicable laws Perform batch record review and input in process data in real time Review cleaning documentation and address any GDP issues Track and ensure batch record corrections are performed and reviewed within the required time frame Support change control activities and edit documents as needed Required to gown with proper PPE in a Grade C environment and work in an area with radioactive materials Perform production system verification checks for batches on the production line Assist with implementation of process improvements BSc in Life Sciences and/or related work experience (pharmaceutical manufacturing) 3-5 years of related experience in cGMP/FDA regulated industry Ability to collaborate with other groups, teams and departments in addressing production, production, and quality assurance-related issues Strong interpersonal, written, communication skills along with problem solving and follow-up skills are required Must be well organized, flexible and work with minimal supervision Ability to lead through influence Strong sense of ownership and accountability Ability to adapt and learn new systems Demonstrate a high level of discipline and self-motivation Provides innovative solutions to complex or process improvement issues", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 171814964691, "name": "Manufacturing Support Associate ", "location": "East Hanover, NJ", "locations": ["East Hanover, NJ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1684780855, "t_create": 1684780827, "ats_job_id": 171814964691, "display_job_id": 171814964691, "type": "ATS", "id_locale": "171814964691-en", "job_description": "This is a temporary contractor opportunity at Novartis Novartis touches the lives of a tenth of the world's population. Every role here, regardless of contract type, makes an impact on human life! Novartis US partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit www.magnitglobal.com Ready to work with/through Magnit at Novartis? Please read on... Role Purpose Performs the entry of manufacturing and test data into controlled database. Assists with the interpretation of the data, including the visualization of data. Assists with technical reports and procedures under guidance. This position requires a scientific mindset with strong technical and/or engineering interest, understanding of validation concepts, basic understanding of sterile manufacturing, as well as strong ability to work in a matrix organization with interfaces to Mfg, TD, QC, and QA. Major Accountabilities Completes all required trainings on time and stay up to date with training requirements Performs data entry into the Discoverant system for all batches manufactured across multiple sites and supports data queries from the Discoverant system. Support the interpretation and visualization of manufacturing and test data. Contributes to process validation lifecycle activities under guidance. by writing and revising master plans for processes, shipping studies, process capability, processes related activities and ongoing process verification for processes, shipping, and aseptic processing (as applicable). Support Associate Director validation for KPI reporting. Reviews Master Batch Records and associated change controls. Assess revalidation need based on technical changes. Key Performance Indicators Completes data entry into the controlled database (Discoverant) and performs data queries in a timely manner. Delivers results as applicable based on the accountabilities described above. \ufeffPay Rate: $17.86 - $19.64 hourly health, dental, vision, 401k Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe we can reinvent what's possible when we collaborate with courage to ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine the impact you could make here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment with diverse teams representative of the patients and communities we serve. To do our best work we need different viewpoints, which is why here at Magnit, we celebrate diversity and embrace inclusion. As an equal opportunity employer, Magnit is dedicated to building a team that represents a variety of backgrounds, perspectives, and skills. We strive to ensure that we maintain a positive and enriching work environment for all. Accommodation: If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com or 1.862.778.5441", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 171814950429, "name": "Supply Chain - Material Planner Support", "location": "Millburn, NJ", "locations": ["Millburn, NJ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1684512664, "t_create": 1684512606, "ats_job_id": 171814950429, "display_job_id": 171814950429, "type": "ATS", "id_locale": "171814950429-en", "job_description": "Support material planner and supply chain operations in Millburn site. Support material planners at site to ensure raw material are available for production of finish goods. Support the analysis of forecasts estimated by country demands on final product and translates it into material requirements for the site. Raises purchase order requisitions in Dynamics D365 based on estimated material requirements. Follows up on the approval by procurement of the purchase requisition into purchase orders. Helps the material planner with organizational activities for projects related to Dynamics D365 Supports process improvement of the Supply Chain team and operations. Ref. Nr. Service Description and Deliverables 1. o On time availability of raw materials for production. o KPI: No out of stocks -shortages- 2. o All forecast of finished goods is well translated into raw material requirements and planned according to the lead time agreed with vendors. o KPI: 100% Adherence to plan. 3. o Ensure system is up to date with the purchase requirements o KPI: 100% of purchase requirements reflected in the system. 4. o Ensures purchase requirements are approved and translated into purchased orders by procurement o KPI: 100% of purchase requirements approved and converted into purchase orders in the ERP system. 5. o Supports the material planner with coordination of project activities regarding Dynamics D365 implementation o KPI: the outcome of a good coordination is that Millburn team is 100% available when solicited for the project with global team. 6. o Improves the process when possible and documents these enhancements o KPI: 100% of process improvements reflected in documentation like Process Mappings, SOPs, or WIP.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 171814910614, "name": "Quality Control Raw Materials Scientist", "location": "Morris Plains, NJ", "locations": ["Morris Plains, NJ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": null, "t_create": 1684252551, "ats_job_id": 171814910614, "display_job_id": 171814910614, "type": "ATS", "id_locale": "171814910614-en", "job_description": "Perform raw material testing following United States Pharmacopoeia (USP), European Pharmacopoeia (EP) and in-house methods Perform testing on raw materials per using HPLC, GC, UV, FTIR, NIR, wet chemistry and other techniques. Perform all testing and activities compliantly following appropriate SOPs and procedures. Review data generated by other team members. Review QC documents to ensure completeness, accuracy, consistency, and clarity. Perform quality impacting assessments and make decisions. Participate special projects and facilitate any issues that arise. Initiate change controls. Author validation documentation. Independently leads investigations of the highest complexity Drive complex investigations to understand root cause. Participate in OOS/OOE investigation Participate in deviation investigation/CAPA implementation in a timely manner Responsible for evaluating compendial updates against internal methods Serve as Quality Control representative on cross-functional teams. Knowledge of LabWare LIMS and/or other QC data systems. Knowledge of appropriate GMP/GLP quality systems (eSOPs, TEDI, etc.). Plan and schedule activities. Ability to lift 35lbs. In addition to these primary duties, provide coverage for all appropriate areas. Perform other job duties as assigned. BA, or MS in biology, chemistry, biochemistry, microbiology, or other related science. Experience in Analytical Quality Control, method development, or a technical support function. At least 3 years of experience. Thorough knowledge of raw material test methods. Analytical chemistry knowledge to facilitate investigations.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 171814902156, "name": "Quality Control Raw Materials Scientist", "location": "Morris Plains, NJ", "locations": ["Morris Plains, NJ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1684153881, "t_create": 1684153745, "ats_job_id": 171814902156, "display_job_id": 171814902156, "type": "ATS", "id_locale": "171814902156-en", "job_description": "This is a temporary contractor opportunity at Novartis Novartis touches the lives of a tenth of the world's population. Every role here, regardless of contract type, makes an impact on human life! Novartis US partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit www.magnitglobal.com Ready to work with/through Magnit at Novartis? Please read on... Responsibilities: Perform raw material testing following United States Pharmacopoeia (USP), European Pharmacopoeia (EP) and in-house methods Perform testing on raw materials per using HPLC, GC, UV, FTIR, NIR, wet chemistry and other techniques. Perform all testing and activities compliantly following appropriate SOPs and procedures. Review data generated by other team members. Review QC documents to ensure completeness, accuracy, consistency, and clarity. Perform quality impacting assessments and make decisions. Participate special projects and facilitate any issues that arise. Initiate change controls. Author validation documentation. Independently leads investigations of the highest complexity Drive complex investigations to understand root cause. Participate in OOS/OOE investigation Participate in deviation investigation/CAPA implementation in a timely manner Responsible for evaluating compendial updates against internal methods Serve as Quality Control representative on cross-functional teams. Knowledge of LabWare LIMS and/or other QC data systems. Knowledge of appropriate GMP/GLP quality systems (eSOPs, TEDI, etc.). Plan and schedule activities. Ability to lift 35lbs. In addition to these primary duties, provide coverage for all appropriate areas. Perform other job duties as assigned. Experience: BA, or MS in biology, chemistry, biochemistry, microbiology, or other related science. Experience in Analytical Quality Control, method development, or a technical support function. At least 3 years of experience. Thorough knowledge of raw material test methods. Analytical chemistry knowledge to facilitate investigations. Pay Range: $25-$34/hour Health, Dental, Vision, 401k Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe we can reinvent what's possible when we collaborate with courage to ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine the impact you could make here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment with diverse teams representative of the patients and communities we serve. To do our best work we need different viewpoints, which is why here at Magnit, we celebrate diversity and embrace inclusion. As an equal opportunity employer, Magnit is dedicated to building a team that represents a variety of backgrounds, perspectives, and skills. We strive to ensure that we maintain a positive and enriching work environment for all. Accommodation: If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com or 1.862.778.5441.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": null}, {"id": 171814902060, "name": "Biotherapeutics Data Management and Business Analyst", "location": "San Diego, CA", "locations": ["San Diego, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1684195005, "t_create": 1684153418, "ats_job_id": 171814902060, "display_job_id": 171814902060, "type": "ATS", "id_locale": "171814902060-en", "job_description": "This is a temporary contractor opportunity at Novartis Novartis touches the lives of a tenth of the world's population. Every role here, regardless of contract type, makes an impact on human life! Novartis US partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit www.magnitglobal.com Ready to work with/through Magnit at Novartis? Please read on... The NIBR Biologics Center in San Diego is seeking a data management professional with experience in database business analysis to work with biotherapeutics scientists in relation to data migration capture and curation. The successful candidate will work with multi-disciplinary biotherapeutics teams to provide support for the unification and capture of biologics data within a global environment and is expected to provide flexible solutions for bridging experimental scientist need with accurate data capture. Responsibilities Work across local and global informatics teams to support and coordinate tasks relating to biotherapeutic data capture and curation. Perform business analysis on legacy database systems to provide solutions for the transfer and unification of data and workflows to a global data management system. Provide robust and practical solutions for the automation, capture and visualization of data relating to protein production workflows including expression, analytics, and biophysics Required Qualifications BSc in Computer Science, informatics, or a related discipline with hands on experience working with databases, data capture or application engineering. A working knowledge of Genedata Biologics is a plus. Proficiency in scripting, SQL and data curation with an emphasis on the management of scientific data. Hands-on record of managing and developing data science/visualization applications and pipelines. Team oriented with strong communication \ufeffPay Range: $88.23 - $116.67 Health, Dental, Vision, 401k Location: Onsite, San Diego, CA Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe we can reinvent what's possible when we collaborate with courage to ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine the impact you could make here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment with diverse teams representative of the patients and communities we serve. 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