CSL Plasma
Principal Scientist, Regulatory Toxicology(m/w/x)
Full-timeOn-siteSenior
Opfikon
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CSCSL Behring
Principal Scientist, Toxicology(m/w/x)
Opfikon
Full-timeOn-siteSenior
Nejo AI Summary
Designing nonclinical safety strategies for biotherapeutic drug development. 5-8 years pharma/biotech experience with GLP and regulatory submissions required. 4-week workation option.
Requirements
- PhD, DVM, or equivalent in Toxicology, Pharmacology, or related field
- 5-8 years of experience in pharmaceutical or biotech industry
- Proven track record in nonclinical safety assessment and regulatory submissions
- Strong understanding of GLP regulations, ICH guidelines, and global regulatory requirements
- Excellent communication, leadership, and cross-functional collaboration skills
- Experience with CSL’s disease therapeutic areas
- Experience across multiple therapeutic areas and modalities
Tasks
- Lead and manage nonclinical safety strategies for drug development projects
- Serve as the primary toxicology representative on interdisciplinary project teams
- Lead the Nonclinical Expert Team (NCET)
- Provide scientific leadership from early discovery to regulatory submission
- Design and monitor nonclinical safety studies in GLP and non-GLP environments
- Compile toxicological risk assessments for drug development projects
- Prepare and review regulatory nonclinical submission documents
- Collaborate with pharmacology, PK, clinical, regulatory, and CMC teams
- Present integrated safety assessments to senior management
- Identify and manage safety risks early in development
- Compile risk assessments for impurities, extractables, leachables, and excipients
- Stay updated on toxicology guidelines and risk assessment methodologies
Work Experience
- 5 - 8 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring 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.
Not a perfect match?
- CSL Behring
Principal Scientist, Regulatory Toxicology(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - CSL Behring
Senior Scientist, Regulatory Toxicology(m/w/x)
Full-timeOn-siteSeniorOpfikon - CSL Behring
Principal Scientist, Pharmacokinetics (PK)(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - CSL Behring
Director, Non-clinical Pharmacology CVR(m/w/x)
Full-timeOn-siteSeniorSchlieren
CSCSL Behring
Principal Scientist, Toxicology(m/w/x)
Opfikon
Full-timeOn-siteSenior
Nejo AI Summary
Designing nonclinical safety strategies for biotherapeutic drug development. 5-8 years pharma/biotech experience with GLP and regulatory submissions required. 4-week workation option.
Requirements
- PhD, DVM, or equivalent in Toxicology, Pharmacology, or related field
- 5-8 years of experience in pharmaceutical or biotech industry
- Proven track record in nonclinical safety assessment and regulatory submissions
- Strong understanding of GLP regulations, ICH guidelines, and global regulatory requirements
- Excellent communication, leadership, and cross-functional collaboration skills
- Experience with CSL’s disease therapeutic areas
- Experience across multiple therapeutic areas and modalities
Tasks
- Lead and manage nonclinical safety strategies for drug development projects
- Serve as the primary toxicology representative on interdisciplinary project teams
- Lead the Nonclinical Expert Team (NCET)
- Provide scientific leadership from early discovery to regulatory submission
- Design and monitor nonclinical safety studies in GLP and non-GLP environments
- Compile toxicological risk assessments for drug development projects
- Prepare and review regulatory nonclinical submission documents
- Collaborate with pharmacology, PK, clinical, regulatory, and CMC teams
- Present integrated safety assessments to senior management
- Identify and manage safety risks early in development
- Compile risk assessments for impurities, extractables, leachables, and excipients
- Stay updated on toxicology guidelines and risk assessment methodologies
Work Experience
- 5 - 8 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring 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.
About the Company
CSL Behring
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein globaler Marktführer in der Biotherapeutik, der innovative Therapien für Patienten mit immunologischen, hämatologischen, kardiovaskulären und anderen Erkrankungen entwickelt.
Not a perfect match?
- CSL Plasma
Principal Scientist, Regulatory Toxicology(m/w/x)
Full-timeOn-siteSeniorOpfikon - CSL Behring
Principal Scientist, Regulatory Toxicology(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - CSL Behring
Senior Scientist, Regulatory Toxicology(m/w/x)
Full-timeOn-siteSeniorOpfikon - CSL Behring
Principal Scientist, Pharmacokinetics (PK)(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - CSL Behring
Director, Non-clinical Pharmacology CVR(m/w/x)
Full-timeOn-siteSeniorSchlieren