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Expert Toxicologist for Impurity Safety Assessment and Risk Management(m/w/x)
Risk assessment of genotoxic impurities per ICH M7 and E&L profiles for pharmaceutical safety dossiers. PhD/MSc in Toxicology and profound ICH guidelines knowledge required. Work in global pharmaceutical company with 100,000+ employees.
Requirements
- PhD and MSc in Toxicology
- 5–10 years in pharmaceutical toxicology
- Working knowledge of genetic toxicology
- Profound knowledge of ICH guidelines
- Broad understanding of drug development
- Strong communication and interpersonal skills
Tasks
- Serve as the main contact for impurity and E&L risk assessments.
- Conduct risk assessments of genotoxic impurities per ICH M7.
- Perform toxicological evaluations of E&L profiles for various components.
- Provide guidance on toxicological concern thresholds for safety dossiers.
- Design and interpret in silico (Q)SAR analyses and propose studies.
- Draft scientifically justified TBLs for impurities and leachables.
- Apply risk assessment methodologies according to ICH and EMA/FDA guidelines.
- Support integration of TBLs into product specifications and validation.
- Collaborate with teams to ensure compliant control strategies.
- Work closely with chemists, scientists, and regulatory affairs teams.
- Evaluate data for the release of new manufacturing batches.
- Represent Roche in industry consortia and regulatory discussions.
- Advise project teams on regulatory requests regarding impurities.
Work Experience
- 5 - 10 years
Education
- Master's degree
Languages
- English – Business Fluent
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Expert Toxicologist for Impurity Safety Assessment and Risk Management(m/w/x)
Risk assessment of genotoxic impurities per ICH M7 and E&L profiles for pharmaceutical safety dossiers. PhD/MSc in Toxicology and profound ICH guidelines knowledge required. Work in global pharmaceutical company with 100,000+ employees.
Requirements
- PhD and MSc in Toxicology
- 5–10 years in pharmaceutical toxicology
- Working knowledge of genetic toxicology
- Profound knowledge of ICH guidelines
- Broad understanding of drug development
- Strong communication and interpersonal skills
Tasks
- Serve as the main contact for impurity and E&L risk assessments.
- Conduct risk assessments of genotoxic impurities per ICH M7.
- Perform toxicological evaluations of E&L profiles for various components.
- Provide guidance on toxicological concern thresholds for safety dossiers.
- Design and interpret in silico (Q)SAR analyses and propose studies.
- Draft scientifically justified TBLs for impurities and leachables.
- Apply risk assessment methodologies according to ICH and EMA/FDA guidelines.
- Support integration of TBLs into product specifications and validation.
- Collaborate with teams to ensure compliant control strategies.
- Work closely with chemists, scientists, and regulatory affairs teams.
- Evaluate data for the release of new manufacturing batches.
- Represent Roche in industry consortia and regulatory discussions.
- Advise project teams on regulatory requests regarding impurities.
Work Experience
- 5 - 10 years
Education
- Master's degree
Languages
- English – Business Fluent
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Roche
Industry
Pharmaceuticals
Description
The company is dedicated to advancing science and ensuring access to healthcare for everyone.
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