Novartis Group Companies
Principal Scientist, Metabolomics
Novartis Group Companies, Cambridge, Massachusetts, us, 02140
Job Description Summary
We are looking for an enthusiastic, curious, and highly motivated individual with experience in metabolomics and bioanalytical LC-MS to join our Translational Profiling group within the Discovery Sciences department in Cambridge, MA. Our Translational Profiling group is a global team of experts in proteomics, metabolomics, lipidomics, super-resolution microscopy, and data science, with locations in Basel, Switzerland, and Cambridge, MA. As a metabolomics/bioanalytical LC/MS expert you will play a key role in advancing our cutting-edge research and drug discovery programs as well as driving the evaluation and implementation of innovative technologies. This role involves collaboration with scientists and project teams across five major disease areas, all dedicated to creating and delivering transformative therapeutics to patients worldwide.
Responsibilities
Collaborate with project partners to design and execute analytical studies that address the key scientific questions of the drug discovery program. Lead and participate in high impact lipidomics and metabolomics projects within drug discovery programs, spanning from early research to patient translation. Champion innovative technology and cross-disciplinary initiatives for biomedical research, including state-of-the-art analytical methodologies to augment the group's technology portfolio and capabilities. Develop and optimize tools for understanding metabolism and transport, identify disease-associated lipid markers, and study metabolic flux to enable next-generation therapies for patients. Maintain a state-of-the-art lipidomics and metabolomics technology platform by staying current with external technology developments and aligning with internal project requirements and application priorities. Execute all aspects of an analytical study including sample preparation, LC-MS analysis, data processing, and analysis. Document work using the internal documentation system; present key outcomes to the project team and plan follow-up steps to advance the project. Develop and implement new LC-MS methods based on project needs. Contribute to assessing and implementing state-of-the-art analytical methodologies to augment the group's technology portfolio and expand its abilities to elucidate the role of metabolism in diseases and the response to therapeutics. Minimum Requirements
A Ph.D. in analytical chemistry, biochemistry, or a related field with a minimum of 2+ years of postgraduate experience, or an MS or BS degree with 10+ years' experience in pharma/biotech. Expertise in biological mass spectrometry and metabolomics including targeted/multi-targeted LC-MS analyses of endogenous small molecules (metabolites and lipids) and metabolic profiling of samples from complex biological matrices such as cell culture, biofluids, and organ tissues. Expertise in sample preparation and extraction protocols from different cell types, tissues, and biofluids of animal or human origin for MS analysis of endogenous small molecules. Proven experience documenting experiments, data, and results in electronic lab journals or laboratory information management systems. Critical and creative problem-solving skills with independent thinking. Excellent communication and presentation skills for multidisciplinary audiences at various seniority and expertise levels. Strong interpersonal skills to work in a collaborative, matrix environment, fostering partnerships across functional teams; able to share results and inspire others. Salary and Benefits
The salary for this position is expected to range between $103,600 and $192,400 per year. The final salary offered is determined based on factors like relevant skills and experience, and upon joining Novartis will be reviewed periodically. Salary ranges may be updated based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays, and other leaves. To learn more about the culture, rewards and benefits we offer our people click here. EEO and Accessibility
EEO Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If you need a reasonable accommodation for any part of the application process or to perform the essential functions of a position, please send an email to us.reasonableaccommodations@novartis.com and include the job requisition number in your message.
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Collaborate with project partners to design and execute analytical studies that address the key scientific questions of the drug discovery program. Lead and participate in high impact lipidomics and metabolomics projects within drug discovery programs, spanning from early research to patient translation. Champion innovative technology and cross-disciplinary initiatives for biomedical research, including state-of-the-art analytical methodologies to augment the group's technology portfolio and capabilities. Develop and optimize tools for understanding metabolism and transport, identify disease-associated lipid markers, and study metabolic flux to enable next-generation therapies for patients. Maintain a state-of-the-art lipidomics and metabolomics technology platform by staying current with external technology developments and aligning with internal project requirements and application priorities. Execute all aspects of an analytical study including sample preparation, LC-MS analysis, data processing, and analysis. Document work using the internal documentation system; present key outcomes to the project team and plan follow-up steps to advance the project. Develop and implement new LC-MS methods based on project needs. Contribute to assessing and implementing state-of-the-art analytical methodologies to augment the group's technology portfolio and expand its abilities to elucidate the role of metabolism in diseases and the response to therapeutics. Minimum Requirements
A Ph.D. in analytical chemistry, biochemistry, or a related field with a minimum of 2+ years of postgraduate experience, or an MS or BS degree with 10+ years' experience in pharma/biotech. Expertise in biological mass spectrometry and metabolomics including targeted/multi-targeted LC-MS analyses of endogenous small molecules (metabolites and lipids) and metabolic profiling of samples from complex biological matrices such as cell culture, biofluids, and organ tissues. Expertise in sample preparation and extraction protocols from different cell types, tissues, and biofluids of animal or human origin for MS analysis of endogenous small molecules. Proven experience documenting experiments, data, and results in electronic lab journals or laboratory information management systems. Critical and creative problem-solving skills with independent thinking. Excellent communication and presentation skills for multidisciplinary audiences at various seniority and expertise levels. Strong interpersonal skills to work in a collaborative, matrix environment, fostering partnerships across functional teams; able to share results and inspire others. Salary and Benefits
The salary for this position is expected to range between $103,600 and $192,400 per year. The final salary offered is determined based on factors like relevant skills and experience, and upon joining Novartis will be reviewed periodically. Salary ranges may be updated based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays, and other leaves. To learn more about the culture, rewards and benefits we offer our people click here. EEO and Accessibility
EEO Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If you need a reasonable accommodation for any part of the application process or to perform the essential functions of a position, please send an email to us.reasonableaccommodations@novartis.com and include the job requisition number in your message.
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