Associate Expert Science
2 settimane fa
SummaryLocation: Ivrea, Italy #HybridRole PurposePlan, perform and report scientific experiments with SME (subject matter expert) to support the project portfolio and/or advance the innovation technical platform of radiopharmaceutical parenteral dosage forms. Contribute to maintenance of laboratory instruments/infrastructure.Please note that this role will be based 100% in IvreaAbout The RoleMajor ActivitiesPlan together with FPL (formulation project leader) and perform formulation development, characterization studies and experiments.Ensure correct, comprehensible, structured, complete and legible documentation according to SOPs, HSE and AdAcAp / Novartis Guidelines.Meet quality, quantity and timelines in all assigned projects. Ensure all own activities are aligned with overall drug development process.Ensure correct and timely filling of logbooks and eLN experiments as per local procedures.Ensure strict adherence to HSE rules and guidelines. Strictly respect existing laboratory workflows (e.g. shipments and materials management).Plan together with AE (analytical expert) and execute analytical tests and analytical method development tests to support formulation and process development (e.g. HPLC chemical and radiochemical purity methods, content by UV, identity, pH, osmolality, visible particles)Participate to the transfer of analytical and/or manufacturing procedures.Ensure training is up-to-date and on time; no overdue training assignments without acceptable cause.Provide documentation of raw data and contribute to interpretation of the results.Keep record of chemicals, intermediates, excipients and solvents within own area of responsibility.Work actively to create lab procedures, reports and/or instructions and/or SOP’s.Contribute to the evaluation of new lab equipment and prepare CAR and USR if applicable.Ensure contribution to networks/workstreams/initiatives and ensure sharing of actions and learnings across the local or global teams as applicable.Impact On The OrganizationSupport RLT drug development and drug manufacturing by delivering drug products procedures and processesIdeal BackgroundEducationMaster’s degree in a scientific field with a minimum of 1-3 years of relevant experience within the pharmaceutical/biotech industryLanguagesGood knowledge of English (oral and written). Fluent knowledge of site languageRequirementsExperience / Professional requirementsAwareness for safe handling of chemicals, potentially dangerous materials and equipment.Adequate scientific or technical knowledge in a specific area (e.g. synthetic, analytical, pharmaceutical).Good knowledge of quality control and production of pharmaceuticalsAdequate knowledge in scientific/technical areas of collaboration.Good knowledge of laboratory and/or technical tools.Adequate knowledge of software and computer tools.Basic presentation skills and scientific/technical writing skillsCommitment to Diversity and InclusionNovartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.Why Novartis:Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? and Rewards:Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:
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Associate Expert Science
1 settimana fa
Ivrea, Piemonte, Italia Novartis A tempo pienoJob Description SummaryLocation: Ivrea, Italy #HybridRole Purpose:Plan, perform and report scientific experiments with SME (subject matter expert) to support the project portfolio and/or advance the innovation technical platform of radiopharmaceutical parenteral dosage forms. Contribute to maintenance of laboratory instruments/infrastructure.**Please note...
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Senior Expert Science
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Ivrea, Italia Novartis Pharma Schweiz A tempo pienoSenior Expert Science & Technology RadiochemistryJoin to apply for the Senior Expert Science & Technology Radiochemistry role at Novartis Pharma SchweizLocation: Ivrea, Italy #hybrid working, onsiteRole PurposeThe Senior Expert Radiochemistry will provide specialized knowledge and expertise as Subject Matter Expert (SME) of radioisotope production and...
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Senior Expert Science
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ivrea, Italia Novartis Pharma Schweiz A tempo pienoSenior Expert Science & Technology RadiochemistryJoin to apply for the Senior Expert Science & Technology Radiochemistry role at Novartis Pharma SchweizLocation: Ivrea, Italy #hybrid working, onsiteRole PurposeThe Senior Expert Radiochemistry will provide specialized knowledge and expertise as Subject Matter Expert (SME) of radioisotope production and...
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Senior Expert Science
1 settimana fa
Ivrea, Piemonte, Italia Novartis A tempo pienoJob Description SummaryLocation: Ivrea, Italy #hybrid working, onsite Role Purpose:The Senior Expert Radiochemistry will provide specialized knowledge and expertise as Subject Matter Expert (SME) of radioisotope production and purification with particular focus on developing radiochemical and separation technologies, target preparation and nuclide...
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Senior Expert Science
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ivrea, Italia Altro A tempo pienoSummaryLocation: Ivrea, Italy#hybrid working, onsiteRole PurposeThe Senior Expert Radiochemistry will provide specialized knowledge and expertise as Subject Matter Expert (SME) of radioisotope production and purification with particular focus on developing radiochemical and separation technologies, target preparation and nuclide identification. Key...
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Pilot Plant Quality Control Associate Expert
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Ivrea, Italia Novartis Pharma Schweiz A tempo pienoPilot Plant Quality Control Associate Expert 2 weeks ago Be among the first 25 applicants Executes analyses on excipients, raw materials, finished products, and packaging per internal SOPs and applicable pharmacopeias. Conducts stability studies, process and method validations, and activities related to tech transfer of pharmaceutical products. Performs...
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Validation Expert
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Ivrea, Italia Novartis Italia A tempo pienoSummary The Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions. About The Role Major accountabilities Support site...
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Validation Expert
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ivrea, Italia Jobs for Humanity A tempo pienoSummaryThe Validation Expert is responsible for executing and managing process primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions.About the RoleMajor accountabilities :Support site validation...
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Validation Expert
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Ivrea, Italia Jobs for Humanity A tempo pienoSummary The Validation Expert is responsible for executing and managing process primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions. About the Role Major accountabilities : Support site...
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Pilot Plant Quality Control Associate Expert
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Ivrea, Italia Novartis Italia A tempo pienoSummary Location: Ivrea, Italy #onsite Role Purpose 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 & current Compendia. About The Role Key responsibilities: Executes analyses on excipients, raw...
