Apply for Cadila Pharmaceuticals Regulatory Affairs jobs 2026. Check salary, eligibility, EU UK AUS NZ experience, and application details now.
Introduction
Experienced regulatory professionals looking to work with global pharmaceutical markets have a strong opportunity here. The Regulatory Affairs Jobs at Cadila Pharmaceuticals Limited offer a senior-level role focused on international submissions and lifecycle management. This position is ideal for candidates with expertise in EU, UK, Australia, and New Zealand regulatory frameworks.
Job Overview
| Details | Information |
|---|---|
| Job Title | Senior Manager – Regulatory Affairs |
| Company Name | Cadila Pharmaceuticals Limited |
| Location | Dholka (near Ahmedabad, Gujarat) |
| Employment Type | Full-Time |
| Department | Regulatory Affairs |
| Experience Required | Experienced Professionals |
| Education | B.Pharm / M.Pharm / M.Sc |
| Salary | ₹18 LPA – ₹28 LPA |
Company Overview
Cadila Pharmaceuticals Limited is a well-established global pharmaceutical company with a strong presence in regulated and semi-regulated markets. Known for its commitment to quality, innovation, and compliance, the company plays a significant role in delivering healthcare solutions worldwide. It offers professionals a dynamic environment to work on international regulatory projects and complex submissions.
Job Location & Employment Type
- Location: Dholka, near Ahmedabad, Gujarat
- Employment Type: Full-Time
The role is based at a key manufacturing and regulatory hub, providing exposure to global operations and compliance standards.
Open Positions / Department Details
- Senior Manager – Regulatory Affairs (EU/UK/AUS/NZ Markets)
This position focuses on handling regulatory submissions and lifecycle management across multiple international markets.
Key Roles & Responsibilities
- Review registration and re-registration dossiers before submission
- Manage regulatory activities for EU, UK, Australia, and New Zealand markets
- Handle pre-approval and post-approval submissions
- Prepare and respond to queries from global health authorities
- Maintain regulatory status of products across different countries
- Coordinate with R&D, QA, and QC teams for compliance and documentation
- Provide technical input for dossier preparation
- Prepare and review variation documents as per international guidelines
- Resolve regulatory challenges related to commercial products
- Support international tender activities aligned with regulatory requirements
- Manage contract manufacturing queries and due diligence activities
Eligibility Criteria
Education
- B.Pharm / M.Pharm / M.Sc in Life Sciences or related fields
Experience
- Proven experience in Regulatory Affairs for EU, UK, AUS, and NZ markets
Skills Required
- Strong knowledge of CTD and eCTD submissions
- Understanding of ICH guidelines and global regulatory frameworks
- Expertise in regulatory lifecycle management
- Hands-on experience in dossier preparation and submission
- Excellent communication and coordination skills
- Ability to manage cross-functional regulatory activities
Salary & Benefits
- Salary: ₹18 LPA – ₹28 LPA (based on experience and expertise)
Additional benefits include:
- Opportunity to work with international regulatory markets
- Exposure to global submission processes
- Career growth in senior regulatory roles
- Collaborative work environment with multiple departments
- Involvement in end-to-end regulatory lifecycle management
Selection Process
The selection process generally includes:
- Resume shortlisting
- Technical/functional interview
- HR discussion
Candidates with strong regulatory experience and international exposure will be preferred.
How to Apply
Interested candidates can apply by sending their updated CV to:
Ensure your resume highlights your experience in global regulatory submissions and lifecycle management.
Important Dates
Candidates are advised to apply early to avoid missing this opportunity.
Why Apply for This Job?
The Regulatory Affairs Jobs at Cadila Pharmaceuticals Limited offer a high-growth opportunity for professionals aiming to advance in global regulatory domains. This role provides direct exposure to international markets, involvement in complex submissions, and leadership-level responsibilities. It is an ideal position for candidates seeking long-term growth in regulatory affairs.
FAQs
1. Who can apply for this job?
Candidates with B.Pharm, M.Pharm, or M.Sc and experience in international regulatory markets can apply.
2. What is the salary range for this role?
The salary ranges between ₹18 LPA to ₹28 LPA depending on experience.
3. Is international regulatory experience required?
Yes, experience in EU, UK, AUS, and NZ markets is essential.
4. How can I apply for this job?
You can apply by sending your CV to savitri.thakor@cadilapharma.com.
5. What skills are important for this role?
Knowledge of CTD/eCTD, ICH guidelines, dossier preparation, and lifecycle management is required.
Conclusion
The Regulatory Affairs Jobs at Cadila Pharmaceuticals Limited present an excellent opportunity for experienced professionals to work in global regulatory environments. With strong salary potential and career growth, this role is ideal for those looking to advance in international pharmaceutical regulations.
Disclaimer
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