Regulatory Affairs Specialist ( Fix Term contract)
Takeda Pharmaceutical Company(1 month ago)
About this role
Regulatory Affairs Specialist (16-month fixed-term) based in Seoul supporting Takeda’s regulatory activities across the product lifecycle. The role involves implementing regulatory plans, maintaining registrations and compliance, and liaising with internal and external stakeholders including regional RA teams and local authorities. It contributes to regulatory strategy execution and quality system adherence to support product launches and life-cycle management.
Required Skills
- Regulatory Submissions
- Lifecycle Management
- Regulatory Compliance
- Stakeholder Management
- Project Management
- Communication Skills
- Negotiation Skills
- Problem Solving
- SOPs
- Quality Management
+3 more
Qualifications
- University Degree in Life Sciences/Medical Sciences/Pharmacy
About Takeda Pharmaceutical Company
takeda.comTakeda is a patient-focused, R&D-driven global biopharmaceutical company committed to bringing Better Health and a Brighter Future.
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