Takeda
Process Engineer Small Molecules API Process Science (Associate Director)(m/w/x)
Vollzeitmit HomeofficeSenior
Zürich
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CSCSL Behring
Director, Nonclinical Due Diligence & External Innovation(m/w/x)
Glattbrugg, Zürich
Full-timeWith Home OfficeSenior
Nejo AI Summary
Leading nonclinical due diligence for biologics and complex modalities, integrating expert input into risk narratives. Advanced degree and 10+ years nonclinical development experience required. Focus on FIH-enabling requirements and clear communication to non-expert stakeholders.
Requirements
- Advanced degree (Ph.D., D.V.M., or equivalent) in toxicology, pharmacology, or related field
- Toxicology training, board certification preferred
- 10+ years nonclinical development experience with proven due diligence or external innovation experience across geographies
- Strong understanding of FIH-enabling nonclinical requirements, particularly for biologics and complex modalities
- Ability to communicate complex scientific risk clearly to non-expert stakeholders
- Experience across multiple therapeutic areas and modalities highly desirable
- Proven ability to work independently or in a team, meeting goals by managing own timelines
- Experience in cross-functional, multicultural, and international teams
- Excellent communication and analytical skills
- Experience analyzing and presenting research results to scientific and professional audiences
- Strong planning and organizational skills
- Ability to work successfully in a matrix organizational structure
- Strong negotiation skills and ability to identify and engage internal and external expertise
- Good understanding of drug development process, strong knowledge of ICH/GLP
Tasks
- Lead nonclinical due diligence for assigned opportunities
- Integrate expert input into clear risk narratives
- Serve as subject-matter lead for nonclinical due diligence on individual deals
- Execute end-to-end nonclinical due diligence for assets or transactions
- Combine input from Toxicology, PK/QSP, and Nonclinical Pharmacology into coherent assessments
- Identify first-in-human gaps, translational risks, and regulatory limitations
- Propose clear mitigation strategies for identified risks
- Prepare high-quality due diligence reports, executive summaries, and risk tables
- Act as scientific interface to Business Development and Therapeutic Area teams
- Contribute to maintaining and improving nonclinical due diligence frameworks
- Mentor junior contributors and matrix team members
- Escalate complex or high-impact issues to Head of Nonclinical Development
- Chair the NCD Review Committee
Work Experience
- 10 years
Education
- Doctoral / PhD
Languages
- English – 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.
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CSCSL Behring
Director, Nonclinical Due Diligence & External Innovation(m/w/x)
Glattbrugg, Zürich
Full-timeWith Home OfficeSenior
Nejo AI Summary
Leading nonclinical due diligence for biologics and complex modalities, integrating expert input into risk narratives. Advanced degree and 10+ years nonclinical development experience required. Focus on FIH-enabling requirements and clear communication to non-expert stakeholders.
Requirements
- Advanced degree (Ph.D., D.V.M., or equivalent) in toxicology, pharmacology, or related field
- Toxicology training, board certification preferred
- 10+ years nonclinical development experience with proven due diligence or external innovation experience across geographies
- Strong understanding of FIH-enabling nonclinical requirements, particularly for biologics and complex modalities
- Ability to communicate complex scientific risk clearly to non-expert stakeholders
- Experience across multiple therapeutic areas and modalities highly desirable
- Proven ability to work independently or in a team, meeting goals by managing own timelines
- Experience in cross-functional, multicultural, and international teams
- Excellent communication and analytical skills
- Experience analyzing and presenting research results to scientific and professional audiences
- Strong planning and organizational skills
- Ability to work successfully in a matrix organizational structure
- Strong negotiation skills and ability to identify and engage internal and external expertise
- Good understanding of drug development process, strong knowledge of ICH/GLP
Tasks
- Lead nonclinical due diligence for assigned opportunities
- Integrate expert input into clear risk narratives
- Serve as subject-matter lead for nonclinical due diligence on individual deals
- Execute end-to-end nonclinical due diligence for assets or transactions
- Combine input from Toxicology, PK/QSP, and Nonclinical Pharmacology into coherent assessments
- Identify first-in-human gaps, translational risks, and regulatory limitations
- Propose clear mitigation strategies for identified risks
- Prepare high-quality due diligence reports, executive summaries, and risk tables
- Act as scientific interface to Business Development and Therapeutic Area teams
- Contribute to maintaining and improving nonclinical due diligence frameworks
- Mentor junior contributors and matrix team members
- Escalate complex or high-impact issues to Head of Nonclinical Development
- Chair the NCD Review Committee
Work Experience
- 10 years
Education
- Doctoral / PhD
Languages
- English – 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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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.
Noch nicht perfekt?
- Takeda
Process Engineer Small Molecules API Process Science (Associate Director)(m/w/x)
Vollzeitmit HomeofficeSeniorZürich - Takeda Development Center Americas, Inc.
Associate Director, Global Regulatory Affairs, Advertising and Promotion(m/w/x)
Vollzeitmit HomeofficeSeniorZürich - Merck & Co., Inc., Rahway, NJ, USA
Associate Director – Global Market Access – Sustainable Access Solutions(m/w/x)
Vollzeitmit HomeofficeSeniorZürich - CSL Behring
Senior Counsel, CMO & Global Supply Chain(m/w/x)
Vollzeitmit HomeofficeSeniorBern, Zürich, Sankt Gallen - ICON plc
Senior Specialist - Medical Information(m/w/x)
VollzeitRemoteSeniorZürich