Cadila Pharmaceuticals is inviting applications for the position of AVP – Regulatory Affairs (ROW + Domestic) – Formulation. This is an excellent opportunity for experienced pharmaceutical regulatory professionals looking for senior leadership jobs in the pharma industry.
Candidates with strong expertise in formulation regulatory affairs, ROW market submissions, domestic regulatory filings, dossier management, and lifecycle management are encouraged to apply. The company is offering an attractive salary package of up to ₹80 LPA for eligible professionals with 16+ years of experience.
This latest pharma regulatory affairs job opening at Cadila Pharmaceuticals is ideal for professionals seeking leadership careers in global pharmaceutical compliance and regulatory strategy.
Job Overview
| Particulars | Details |
|---|---|
| Company | Cadila Pharmaceuticals |
| Department | Regulatory Affairs – Formulation |
| Position | AVP – Regulatory Affairs |
| Qualification | M.Pharm / M.Sc |
| Experience | 16+ Years |
| Salary | Up to ₹80 LPA |
| Industry | Pharmaceutical Industry |
| Location | India |
| Employment Type | Full-Time |
Key Responsibilities
The selected candidate will be responsible for:
- Developing regulatory strategy for ROW and Domestic pharmaceutical markets
- Compilation, review, and submission of regulatory dossiers
- Managing regulatory filings for formulation products
- Coordinating with cross-functional departments for timely approvals
- Handling regulatory deficiencies, agency queries, and lifecycle management
- Ensuring compliance with global and domestic regulatory guidelines
- Leading stakeholder communication and regulatory project execution
- Supporting business growth through effective regulatory planning
Desired Candidate Profile
Cadila Pharmaceuticals is looking for professionals with:
- Strong exposure to Formulation Regulatory Affairs
- Hands-on experience in ROW and Domestic market submissions
- Excellent understanding of regulatory documentation and compliance
- Leadership and stakeholder management expertise
- Proven experience in handling regulatory audits and approvals
- Strong communication and team coordination abilities
Qualification & Experience
Educational Qualification
- M.Pharm
- M.Sc
Experience Required
- Minimum 16+ years in pharmaceutical regulatory affairs
Salary & Benefits
Cadila Pharmaceuticals is offering:
- Salary package up to ₹80 Lakhs Per Annum
- Senior leadership role in regulatory affairs
- Exposure to global pharmaceutical regulatory markets
- Opportunity to work with cross-functional pharma teams
- Career growth in a reputed pharmaceutical organization
How to Apply
Interested candidates can share their updated CV with the subject line:
“Application for AVP – Regulatory Affairs”
Email ID: drashti.chaudhari@cadilapharma.com
