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NONovartis Pharma AG

Senior Expert Science & Technology(m/w/x)

Basel
Full-timeOn-siteSenior

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

  • EnglishBusiness Fluent

Tools & Technologies

  • mass spectrometry
  • HPLC
  • UV-spectrometry
  • titration

Benefits

Other Benefits

  • Reasonable accommodation for medical condition or disability
  • Inclusion support
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis Pharma AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.

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