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APAC/LATAM Regulatory Affairs Hematology Lead (Senior Director)(m/w/x)
Crafting market access strategies for blood-related biotherapies, managing health authority relationships in diverse regional markets. 10+ years international pharmaceutical compliance and leadership experience required; biologics background preferred. Extensive cross-cultural collaboration with international stakeholders.
Requirements
- Advanced degree in Life Science or Business with a postgraduate qualification (PhD, MD, MBA or other)
- 15+ years' experience in the pharmaceutical industry
- At least 10 years' experience in Global Regulatory Affairs
- Biologics regulatory experience preferred
- 10+ years' leadership experience
- Experience managing global regulatory teams
Tasks
- Drive and implement innovative regional regulatory strategies for APAC/LATAM
- Execute comprehensive regulatory activities aligned with global standards
- Manage CSL's relationship with health authorities in the region
- Foster empowerment and capability-building initiatives for the regulatory team
- Establish effective communication channels among local and global stakeholders
- Represent global regulatory in health authority inspections and strategic meetings
Work Experience
- 15 years
Education
- Master's degree
Languages
- English – Business Fluent
Not a perfect match?
- CSL Behring L.L.C.Full-timeOn-siteSeniorGlattbrugg
- CSL Behring AG (CH)
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APAC/LATAM Regulatory Affairs Hematology Lead (Senior Director)(m/w/x)
Crafting market access strategies for blood-related biotherapies, managing health authority relationships in diverse regional markets. 10+ years international pharmaceutical compliance and leadership experience required; biologics background preferred. Extensive cross-cultural collaboration with international stakeholders.
Requirements
- Advanced degree in Life Science or Business with a postgraduate qualification (PhD, MD, MBA or other)
- 15+ years' experience in the pharmaceutical industry
- At least 10 years' experience in Global Regulatory Affairs
- Biologics regulatory experience preferred
- 10+ years' leadership experience
- Experience managing global regulatory teams
Tasks
- Drive and implement innovative regional regulatory strategies for APAC/LATAM
- Execute comprehensive regulatory activities aligned with global standards
- Manage CSL's relationship with health authorities in the region
- Foster empowerment and capability-building initiatives for the regulatory team
- Establish effective communication channels among local and global stakeholders
- Represent global regulatory in health authority inspections and strategic meetings
Work Experience
- 15 years
Education
- Master's degree
Languages
- English – Business Fluent
About the Company
CSL Behring L.L.C.
Industry
Pharmaceuticals
Description
The company is a global biotherapeutics leader focused on developing innovative therapies for various medical conditions.
Not a perfect match?
- CSL Behring L.L.C.
Sr. Dir., Global Regulatory Team Leader – Hematology & LCM Europe(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - CSL Behring AG (CH)
Regional Regulatory Lead – APAC, LATAM & Partner Business(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - Merck & Co., Inc.
Regional Director of Medical Affairs, Hematology (MER & EEMEA Region)(m/w/x)
Full-timeOn-siteSeniorZürich - CSL Behring
Senior Director, Head of Translational Research Hematology & CVR(m/w/x)
Full-timeOn-siteManagementSchlieren - Takeda Pharmaceuticals International AG
GRA CMC Director - Marketed Products Development Lead(m/w/x)
Full-timeOn-siteManagementZürich