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Senior Expert Science & Technology(m/w/x)
Designing and executing scientific experiments for ARD Oligonucleotides Analytics project. PhD with 3 years' experience or Master's with 10 years' experience required. Inclusion support, reasonable accommodation for medical condition.
Requirements
- PhD with 3 years' experience or Master's with 10 years' experience in pharmaceutical industry
- Proficiency in hyphenated analytical separation and detection techniques including mass spectrometry
- Excellent knowledge of general laboratory management and analytical techniques (HPLC, UV-spectrometry, titration)
- Proven experience in quality principles driving drug development (GMP); understanding of regulatory and quality expectations
- Ability to perform in a highly dynamic environment
- Strong coordination, clear communication, teamwork, self-motivation, and quick learning
Tasks
- Design and execute scientific experiments
- Report results for ARD Oligonucleotides Analytics project
- Ensure timely delivery of supplies and knowledge
- Lead and manage project and team activities
- Contribute to analytical strategy
- Promote scientific and operational excellence
- Design and plan analytical activities for oligonucleotides
- Execute and interpret analytical methods
- Report analytical results according to timelines and standards
- Develop and apply mass spectrometry methods
- Foster and share best practices
- Provide scientific and technical expertise
- Create analytical documents aligned with project strategies
- Assist in strategic planning and execution
- Plan and implement laboratory experiments
- Schedule and monitor experimental activities
- Analyze and report data
- Serve as main contact for science and technical issues
- Offer scientific guidance to laboratory associates
- Oversee technical analytical deviations
- Recommend corrective and preventive actions
- Assist with audits and health authority inspections
- Ensure compliance with SOPs, GMP, GLP, QM, HSE, ISRM, and Novartis Guidelines
- Collaborate and share expertise
Work Experience
- 3 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- mass spectrometry
- HPLC
- UV-spectrometry
- titration
Benefits
Other Benefits
- Reasonable accommodation for medical condition or disability
- Inclusion support
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Senior Expert Science & Technology(m/w/x)
Designing and executing scientific experiments for ARD Oligonucleotides Analytics project. PhD with 3 years' experience or Master's with 10 years' experience required. Inclusion support, reasonable accommodation for medical condition.
Requirements
- PhD with 3 years' experience or Master's with 10 years' experience in pharmaceutical industry
- Proficiency in hyphenated analytical separation and detection techniques including mass spectrometry
- Excellent knowledge of general laboratory management and analytical techniques (HPLC, UV-spectrometry, titration)
- Proven experience in quality principles driving drug development (GMP); understanding of regulatory and quality expectations
- Ability to perform in a highly dynamic environment
- Strong coordination, clear communication, teamwork, self-motivation, and quick learning
Tasks
- Design and execute scientific experiments
- Report results for ARD Oligonucleotides Analytics project
- Ensure timely delivery of supplies and knowledge
- Lead and manage project and team activities
- Contribute to analytical strategy
- Promote scientific and operational excellence
- Design and plan analytical activities for oligonucleotides
- Execute and interpret analytical methods
- Report analytical results according to timelines and standards
- Develop and apply mass spectrometry methods
- Foster and share best practices
- Provide scientific and technical expertise
- Create analytical documents aligned with project strategies
- Assist in strategic planning and execution
- Plan and implement laboratory experiments
- Schedule and monitor experimental activities
- Analyze and report data
- Serve as main contact for science and technical issues
- Offer scientific guidance to laboratory associates
- Oversee technical analytical deviations
- Recommend corrective and preventive actions
- Assist with audits and health authority inspections
- Ensure compliance with SOPs, GMP, GLP, QM, HSE, ISRM, and Novartis Guidelines
- Collaborate and share expertise
Work Experience
- 3 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- mass spectrometry
- HPLC
- UV-spectrometry
- titration
Benefits
Other Benefits
- Reasonable accommodation for medical condition or disability
- Inclusion support
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Novartis Pharma AG
Industry
Pharmaceuticals
Description
Das Unternehmen setzt sich für Vielfalt, Chancengleichheit und Inklusion ein und fördert innovative Lösungen zur Verbesserung der Patientenversorgung.
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