Regulatory Affairs Specialist
3 weeks ago
Job Summary
We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Takeda. As a key member of our Regulatory Affairs department, you will be responsible for leading and developing regulatory strategies for new products, existing products, and pipeline molecules across various regions.
Key Responsibilities
- Develop and implement regulatory strategies to ensure compliance with local and global regulations
- Lead cross-functional teams to ensure timely submission of regulatory dossiers and approvals
- Collaborate with internal stakeholders to ensure alignment with business plans and strategies
- Stay up-to-date with changes in local and global regulations and communicate effectively with key stakeholders
Requirements
- Bachelor's degree in Pharmacy or Masters in Chemistry, Sciences, Biotechnology, Biomedical Engineering, Microbiology, or equivalent degree
- 8-10 years of experience in Pharmaceutical, Medical Device, CRO industry
- Strong knowledge of local regulations and regulatory corporate policies
- Excellent verbal and written communication skills
- Project management and stakeholder management skills
What We Offer
- A dynamic and supportive work environment
- Opportunities for professional growth and development
- A competitive salary and benefits package
How to Apply
If you are a motivated and experienced Regulatory Affairs professional looking for a new challenge, please submit your application.
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