Company Overview: Takeda Pharmaceutical Company is a global leader in developing medicines that improve patient lives. With over 30,000 employees across 70 countries, we focus on oncology, gastroenterology, neuroscience, and vaccines. We’re expanding our operations in India and need a dedicated leader to drive our regulatory affairs.
Job Title: Head of Regulatory Affairs, India
Location: Gurgaon, India
Job Description: As the Head of Regulatory Affairs in India, you will:
- Lead the regulatory strategy for our product portfolio.
- Ensure timely approvals for new products and manage existing products.
- Work with Indian and global teams to meet regulatory requirements.
- Oversee local regulatory compliance for product importation, licensing, and distribution.
- Develop and lead a strong regulatory team.
Key Responsibilities:
- Manage new product registrations and renewals.
- Ensure compliance with both local and global standards.
- Respond to regulatory authority requests quickly.
- Maintain accurate regulatory documentation.
- Develop regulatory strategies that align with marketing plans.
- Train and develop the local regulatory team.
Candidate Requirements:
- 10+ years in Regulatory Affairs within Pharma/Healthcare.
- 5+ years in a leadership role.
- Strong understanding of Indian regulatory requirements and global trends.
- Proven track record in managing regulatory approvals and negotiations.
- Bachelor’s degree in Science or related field.
Personal Traits:
- Strategic thinker with a focus on innovation.
- Excellent communication and leadership skills.
- Ability to drive results and manage teams effectively.
Why Join Us:
- Be a key player in expanding Takeda’s presence in India.
- Lead the introduction of new treatments and vaccines to meet patient needs.
- Work in a dynamic and growing organization with a commitment to improving lives.
Application Deadline: September 30, 2024
