Executive International Regulatory Affairs – Regulatory Affairs | Juvencia Lifesciences | Ahmedabad, Gujarat, India
Juvencia Lifesciences is hiring an Executive International Regulatory Affairs in Ahmedabad for its pharmaceutical operations. This role is ideal for candidates with 3–4 years of experience in regulatory submissions, dossier preparation, and compliance for international markets.
Location
Ahmedabad, Gujarat, India
Employment Type
Full-time
Experience Required
3–4 Years
Compensation & Benefits
Not Disclosed
About Juvencia Lifesciences
Juvencia Lifesciences operates in the pharmaceutical sector with a focus on regulatory compliance and global market expansion.
Position Overview
The role involves managing international regulatory documentation and ensuring compliance with global standards.
Key Responsibilities
- Prepare regulatory dossiers
- Handle international submissions
- Maintain regulatory documentation
- Ensure compliance with guidelines
- Coordinate with regulatory authorities
- Track submission timelines
- Support audits and inspections
- Maintain regulatory databases
- Coordinate with internal teams
- Ensure product compliance
Required Skills & Competencies
- Regulatory affairs knowledge
- Documentation expertise
- Understanding of global guidelines
- Attention to detail
- Communication skills
- Problem-solving ability
- Analytical thinking
- Team coordination
- Compliance knowledge
- Pharmaceutical experience
Educational Qualification
BPharm
About the Project & Industry
International regulatory affairs in pharmaceutical industry ensuring global approvals.
Why Join Juvencia Lifesciences?
Opportunity to work in global regulatory functions with career growth.
How to Apply
Send your resume to hr@juvencia.in
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