
Regulatory Affairs Expert
1 day ago
The Regulatory Affairs Manager is responsible for leading the execution and coordination of global regulatory activities.
Key Responsibilities:- Develop and execute strategic plans for global and country-specific regulatory compliance
- Provide CMC regulatory strategy by defining filing requirements, submission strategies, and risk assessments
- Lead teams in developing dossiers for CMC content for initial submissions, variations, and amendments
- Facilitate change management activities
- Develop response strategies and respond to health authority questions
- Collaborate with cross-functional teams to align regulatory strategies, timing, and supply plans
- Track and report data on department deliverables
- Doctoral degree or equivalent experience
- Proven experience in manufacturing, quality control, quality assurance, or clinical testing
- Regulatory expertise in CMC
Benefits of working in this role include career growth opportunities, a collaborative work environment, and the chance to make a meaningful impact in the field of regulatory affairs.
This position requires strong leadership skills, excellent communication abilities, and a passion for staying up-to-date with changing regulatory requirements.
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