CSL Behring L.L.C.
APAC/LATAM Regulatory Affairs Hematology Lead (Senior Director)(m/w/x)
Full-timeOn-siteSenior
Glattbrugg
New Job?Nejo!
The AI Job Search Engine
CSCSL Behring AG (CH)
Regional Regulatory Lead – APAC, LATAM & Partner Business(m/w/x)
Glattbrugg
Full-timeOn-siteSenior
Nejo AI Summary
Overseeing drug applications, renewals, and variations for life-saving biotech therapies. Minimum 5 years of international regulatory experience and a life sciences degree required. Global strategy team participation.
Requirements
- Degree in Biological, Medical Sciences, Pharmacy, or related field
- Postgraduate qualifications in Drug Regulatory Affairs as advantage
- Minimum 5 years of international regulatory experience
- Experience in pharmaceutical or biotech industry ideally
- Strong understanding of scientific principles and development
- Knowledge of GMP requirements
- Mandatory fluency in English
- Arabic, French, Spanish, or Russian as asset
- Ability to manage complex regulatory activities
- Ability to influence stakeholders and navigate environments
Tasks
- Define and drive regional regulatory strategies
- Align regional plans with global priorities
- Participate in Global Strategy Teams
- Contribute to complex scientific assessments
- Oversee drug applications, renewals, and variations
- Manage Health Authority interactions and PSURs
- Prepare high-quality regulatory documentation
- Respond to Health Authority inquiries
- Collaborate with local regulatory and internal partners
- Monitor international and regional regulatory changes
- Identify regulatory risks and provide expert guidance
- Support process improvements and training development
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- Arabic – Basic
- French – Basic
- Spanish – Basic
- Russian – Basic
Tools & Technologies
- GMP
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring AG (CH) 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 L.L.C.
Sr. Dir., Global Regulatory Team Leader – Hematology & LCM Europe(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - Takeda Pharmaceuticals International AG
Associate Director, EUCAN Regulatory Lead - GI and Inflammation(m/w/x)
Full-timeOn-siteSeniorZürich - Takeda Pharmaceuticals International AG
Manager, International Clinical Trial Regulatory Lead(m/w/x)
Full-timeOn-siteManagementZürich - Takeda Pharmaceuticals International AG
Associate Director, EUCAN Regulatory Lead - Oncology(m/w/x)
Full-timeOn-siteSeniorZürich
CSCSL Behring AG (CH)
Regional Regulatory Lead – APAC, LATAM & Partner Business(m/w/x)
Glattbrugg
Full-timeOn-siteSenior
Nejo AI Summary
Overseeing drug applications, renewals, and variations for life-saving biotech therapies. Minimum 5 years of international regulatory experience and a life sciences degree required. Global strategy team participation.
Requirements
- Degree in Biological, Medical Sciences, Pharmacy, or related field
- Postgraduate qualifications in Drug Regulatory Affairs as advantage
- Minimum 5 years of international regulatory experience
- Experience in pharmaceutical or biotech industry ideally
- Strong understanding of scientific principles and development
- Knowledge of GMP requirements
- Mandatory fluency in English
- Arabic, French, Spanish, or Russian as asset
- Ability to manage complex regulatory activities
- Ability to influence stakeholders and navigate environments
Tasks
- Define and drive regional regulatory strategies
- Align regional plans with global priorities
- Participate in Global Strategy Teams
- Contribute to complex scientific assessments
- Oversee drug applications, renewals, and variations
- Manage Health Authority interactions and PSURs
- Prepare high-quality regulatory documentation
- Respond to Health Authority inquiries
- Collaborate with local regulatory and internal partners
- Monitor international and regional regulatory changes
- Identify regulatory risks and provide expert guidance
- Support process improvements and training development
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- Arabic – Basic
- French – Basic
- Spanish – Basic
- Russian – Basic
Tools & Technologies
- GMP
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring AG (CH) 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 AG (CH)
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein weltweit führendes Biotech-Unternehmen, das lebensrettende Therapien für Menschen mit schweren und seltenen Krankheiten entwickelt und vertreibt.
Not a perfect match?
- CSL Behring L.L.C.
APAC/LATAM Regulatory Affairs Hematology Lead (Senior Director)(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - CSL Behring L.L.C.
Sr. Dir., Global Regulatory Team Leader – Hematology & LCM Europe(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - Takeda Pharmaceuticals International AG
Associate Director, EUCAN Regulatory Lead - GI and Inflammation(m/w/x)
Full-timeOn-siteSeniorZürich - Takeda Pharmaceuticals International AG
Manager, International Clinical Trial Regulatory Lead(m/w/x)
Full-timeOn-siteManagementZürich - Takeda Pharmaceuticals International AG
Associate Director, EUCAN Regulatory Lead - Oncology(m/w/x)
Full-timeOn-siteSeniorZürich