Regulatory Affairs AGM – Regulatory Affairs | Cadila Pharmaceuticals | Ahmedabad (Dholka), Gujarat, India
Cadila Pharmaceuticals is hiring a Regulatory Affairs AGM in Dholka, Ahmedabad for its pharmaceutical operations. This senior leadership role is ideal for professionals with 15–20 years of experience in regulatory affairs, global submissions, and compliance management.
Location
Ahmedabad (Dholka), Gujarat, India
Employment Type
Full-time
Experience Required
15–20 Years
Compensation & Benefits
Not Disclosed
About Cadila Pharmaceuticals
Cadila Pharmaceuticals is a leading pharmaceutical company known for innovation, global regulatory presence, and high-quality manufacturing.
Position Overview
The AGM Regulatory Affairs will lead regulatory strategy, submissions, and compliance for domestic and international markets.
Key Responsibilities
- Lead regulatory strategy and planning
- Manage global regulatory submissions
- Ensure compliance with regulatory guidelines
- Coordinate with international authorities
- Review dossiers and documentation
- Handle audits and inspections
- Lead regulatory teams
- Maintain regulatory databases
- Ensure timely approvals
- Drive compliance initiatives
Required Skills & Competencies
- Regulatory affairs leadership
- Knowledge of global guidelines
- Documentation expertise
- Communication skills
- Leadership ability
- Analytical thinking
- Problem-solving ability
- Team management
- Attention to detail
- Compliance knowledge
Educational Qualification
MPharm
About the Project & Industry
Regulatory affairs in pharmaceutical industry ensuring global compliance and approvals.
Why Join Cadila Pharmaceuticals?
Opportunity to lead regulatory operations in a reputed pharmaceutical organization.
How to Apply
Send your resume to bhumika.nagar@cadilapharma.com
Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.