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Analytical Expert
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Network
Projektbeschreibung
Harvey Nash is looking for an Analytical Expert for a 11+ month project in Switzerland.
You are responsible for
- Designing, planning, performing, interpreting and reporting results of scientific experiments for the preparation and timely delivery of drug substances (DS) and drug products (DP)
- analytical methods development, validation, stability and release testing and transfer activities of drug substance and formulated drug product.
- Contributing to the overall analytical project strategy
- Writing analytical documents (eg Analytical methods, Validation reports, Stability reports)
- Ensuring GMP compliance for all GMP relevant analytical activities of assigned projects in alignment with Novartis regulations and network decisions
- Authoring, reviewing and approving of GMP relevant documents (eg analytical methods, raw data, SOPs, qualification reports for analytical instruments, etc.)
- Reviewing analytical batch records according to SOPs
- Supporting defining the analytical strategy of development projects (proposes specifications, re-test dates, storage conditions, and/or batch release decision according to analytical results, SOPs, and Novartis guidelines)
- Reviewing analytical batch records according to SOPs
- Supporting identifying scientific, technological and GMP issues and proposes solutions to relevant persons in the analytical project team
- Demonstrating cost awareness in all assigned projects and/or networks
Requirements
Languages: French and English (both languages prerequisite); German (good asset)
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred) to (see below) For further details feel free to call me. I am looking forward to receiving your application.
You are responsible for
- Designing, planning, performing, interpreting and reporting results of scientific experiments for the preparation and timely delivery of drug substances (DS) and drug products (DP)
- analytical methods development, validation, stability and release testing and transfer activities of drug substance and formulated drug product.
- Contributing to the overall analytical project strategy
- Writing analytical documents (eg Analytical methods, Validation reports, Stability reports)
- Ensuring GMP compliance for all GMP relevant analytical activities of assigned projects in alignment with Novartis regulations and network decisions
- Authoring, reviewing and approving of GMP relevant documents (eg analytical methods, raw data, SOPs, qualification reports for analytical instruments, etc.)
- Reviewing analytical batch records according to SOPs
- Supporting defining the analytical strategy of development projects (proposes specifications, re-test dates, storage conditions, and/or batch release decision according to analytical results, SOPs, and Novartis guidelines)
- Reviewing analytical batch records according to SOPs
- Supporting identifying scientific, technological and GMP issues and proposes solutions to relevant persons in the analytical project team
- Demonstrating cost awareness in all assigned projects and/or networks
Requirements
Languages: French and English (both languages prerequisite); German (good asset)
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred) to (see below) For further details feel free to call me. I am looking forward to receiving your application.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung