Merck KGaA·5 days ago
5 days ago
Associate Director, Global Regulatory Affairs
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What you'll do
- Lead regulatory strategy and execution for assigned projects
- Oversee regulatory submissions
- Collaborate with cross-functional teams
- Ensure compliance
What they're looking for
- Strong background in drug development and FDA/EMA interactions
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
We are looking for an Associate Director, Global Regulatory Affairs to lead regulatory strategy and execution for assigned projects. Oversee regulatory submissions, collaborate with cross-functional teams, and ensure compliance. Ideal for experienced regulatory professionals with a strong background in drug development and FDA/EMA interactions.
Skills
- submission management
- regulatory compliance
- regulatory project management
- stakeholder management
- matrix leadership
- fda strategy
- cross-functional collaboration
- ha interaction
- development submissions
- english proficiency
- project planning
- regulatory strategy
- regulatory affairs
- maintenance submissions
- global regulatory strategy
Company
Merck KGaA
Billerica, United States of America
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