International Regulatory Affairs Executive – Regulatory Affairs | Claps Pharma | Ahmedabad, Gujarat, India
Claps Pharma is hiring an International Regulatory Affairs Executive in Ahmedabad for its pharmaceutical operations. This role is suitable for candidates with 3–5 years of experience in regulatory submissions, documentation, and compliance for international markets.
Location
Ahmedabad, Gujarat, India
Employment Type
Full-time
Experience Required
3–5 Years
Compensation & Benefits
Not Disclosed
About Claps Pharma
Claps Pharma is a pharmaceutical company focused on global regulatory compliance and product development.
Position Overview
The Regulatory Affairs Executive will handle international regulatory submissions and ensure compliance with global standards.
Key Responsibilities
- Prepare regulatory submissions
- Maintain regulatory documentation
- Ensure compliance with international guidelines
- Coordinate with regulatory authorities
- Handle dossier preparation
- Track submission timelines
- Support audits and inspections
- Manage regulatory databases
- Coordinate with internal teams
- Ensure product compliance
Required Skills & Competencies
- Regulatory affairs expertise
- Knowledge of international guidelines
- Documentation skills
- Attention to detail
- Communication skills
- Problem-solving ability
- Pharmaceutical industry experience
- Analytical thinking
- Team coordination
- Compliance knowledge
Educational Qualification
MPharm
About the Project & Industry
International regulatory compliance in pharmaceutical manufacturing ensuring global market approvals.
Why Join Claps Pharma?
Opportunity to work in global regulatory affairs with strong exposure to international markets.
How to Apply
Send your resume to hr@clapspharma.com
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