Über das Unternehmen
Roche Diagnostics AG, a division of F. Hoffmann-La Roche AG, is a global pioneer in pharmaceuticals and diagnostics. Based in Switzerland, we are dedicated to advancing science to improve people’s lives. Our commitment to innovation drives us to discover and develop solutions that detect, prevent, and treat diseases, contributing significantly to global health. Join a team that values scientific excellence, integrity, and a passion for making a difference.
Stellenbeschreibung
We are seeking a highly motivated and detail-oriented English Speaking Toxicology Analyst to join our dynamic team in a hybrid capacity, based out of Pontresina. This role is critical in supporting our research and development initiatives by performing in-depth toxicological analysis, interpreting complex data, and ensuring compliance with international regulatory standards. The ideal candidate will possess a strong background in analytical chemistry or toxicology, excellent communication skills in English, and a proactive approach to problem-solving. You will contribute to the safety assessment of novel compounds and existing products, playing a vital role in bringing life-changing solutions to patients worldwide.
Hauptverantwortlichkeiten
- Conduct toxicological analyses of various samples using advanced analytical techniques.
- Interpret and critically evaluate data from in vitro and in vivo toxicology studies.
- Prepare comprehensive reports and presentations detailing findings and conclusions.
- Ensure all laboratory activities comply with Good Laboratory Practice (GLP) and other relevant regulatory guidelines.
- Collaborate cross-functionally with research scientists, regulatory affairs, and project teams.
- Develop and validate new analytical methods and improve existing ones.
- Maintain and calibrate laboratory equipment, ensuring optimal performance and troubleshooting issues as they arise.
- Stay updated with the latest advancements in toxicology and analytical science.
- Contribute to the continuous improvement of laboratory processes and safety protocols.
Erforderliche Fähigkeiten
- Proficiency in English (written and spoken) essential for international collaboration and documentation.
- Demonstrated experience with analytical instruments (e.g., LC-MS, GC-MS, HPLC).
- Strong understanding of toxicological principles and safety assessment methodologies.
- Excellent data analysis, interpretation, and problem-solving skills.
- Ability to work independently and as part of a collaborative team.
- Proficiency in laboratory information management systems (LIMS) and Microsoft Office Suite.
Bevorzugte Qualifikationen
- Master's or Ph.D. in Toxicology, Analytical Chemistry, Pharmacology, or a related scientific field.
- Experience in a GLP-regulated environment.
- Familiarity with European and international regulatory requirements for pharmaceuticals or diagnostics.
- Previous experience in a pharmaceutical or biotechnology industry setting.
- Knowledge of statistical software for data analysis.
Vorteile & Zusatzleistungen
- Competitive salary and performance-based bonuses.
- Comprehensive health, dental, and vision insurance.
- Generous paid time off and holiday schedule.
- Pension scheme and retirement benefits.
- Opportunities for professional development and continuous learning.
- Subsidized public transportation or parking.
- Employee assistance program.
- Access to a modern, well-equipped laboratory environment.
So bewerben Sie sich
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- Einen aktuellen Lebenslauf
- Ein kurzes Anschreiben, das Ihre Erfahrung und Motivation zusammenfasst
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