Oligonucleotide
Pharmaceutical
SeniorExpertScienceandTechnology
Neural analysis suggests this role is
optimal for Senior candidates.
“Senior Expert Science and Technology at Oligonucleotide. Skills: Oligonucleotide analytics, analytical methodologies, chromatography techniques, mass spectrometry, GMP. Design, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures. Lead and manage all project/local network activities”
What You'll Achieve.
timely delivery of drug substances (DS), drug products (DP), processes and procedures; contribute to overall TRD strategies and goals
Industry & Context.
interpret and report results; analytical method developments/validations/transfers/stability/release testing; data evaluation
Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISRM & Novartis Guidelines
What They're Looking For.
Must Have
PhD in Analytical Chemistry (or equivalent) with a minimum of 5 years of experience in pharmaceutical analytical development, expertise in oligonucleotide analytics, Proven expertise in liquid chromatography separation techniques, including RP, IEX, and HILIC (mandatory), Solid GMP experience (mandatory), Sound understanding of regulatory and quality expectations
Nice to Have
Experience in mass spectrometry applied to biological molecules would be an asset, Experience in mass spectrometry, including mass confirmation, impurity quantification, and sequencing (asset)
What You'll Do.
interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS)
processes and procedures
Lead and manage all project/local network activities
develop and validate robust analytical methodologies applied to innovative Oligonucleotides therapeutics
interpret and report analytical activities for DS and/or DP applying state of the art analytical science and technologies
Contribute to the planning and execution of experiments in the lab for assigned projects
Author analytical documents supporting the analytical and the global project strategies based on project phase
Support the elaboration of analytical documents for handover to internal and external partners
Contribute to shaping the Oligonucleotide lab further
alongside experienced experts and scientists and prepare the lab for Oligonucleotide analytics
How You'll Work.
Team & Collaboration
support/coach team members; participate in sub-teams; contribute to overall TRD strategies and goals; share best practices, bring scientific and technical expertise within the analytical project sub team, analytical scientists and across the organization; Embrace the Novartis Values & Behaviors, coach and mentor project team members and other associates; contribute to shaping the Oligonucleotide lab further, alongside experienced experts and scientists
Communication Scope
interpret and report results; Author analytical documents; Support the elaboration of analytical documents; scientific/technical writing; presentations; excellent communication skills
Process & Methodology
Lead and manage all project/local network activities, planning and execution of experiments in the lab for assigned projects (for e. g. , scheduling of activities in the lab, experimental overview, data evaluation)
Full Job Description
**Job Description Summary** Design, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures. Lead and manage all project/local network activities, support/coach team members, participate in sub-teams and contribute to overall TRD strategies and goals. **Job Description** **Key Responsibilities** * Responsible to develop and validate robust analytical methodologies applied to innovative Oligonucleotides therapeutics. Strong experience in various chromatography techniques is a pre-requisite. Experience in mass spectrometry applied to biological molecules would be an asset. * Responsible to design, plan, conduct, interpret and report analytical activities for DS and/or DP applying state of the art analytical science and technologies (e.g., analytical method developments/validations/transfers/stability/release testing, formulation development analytics etc.) according to the agreed timelines and appropriate quality standards. * Contribute to the planning and execution of experiments in the lab for assigned projects (for e.g., scheduling of activities in the lab, experimental overview, data evaluation). * Author analytical documents supporting the analytical and the global project strategies based on project phase. Contribute to strategic decisions: design, plan and execute. * Support the elaboration of analytical documents for handover to internal and external partners (for e.g., including Health authority questions /CMC modules / Manufacturing & supply operations etc.). * Accountable to share best practices, bring strong scientific and technical expertise within the analytical project sub team, analytical scientists and across the organization. * Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISRM & Novartis Guidelines and exhibit strong team spirit and promote knowledge exchange. Embrace the Novartis Values & Behaviors, coach and mentor p
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