DRA Executive Job in Noida 2026 | Regulatory Affairs Pharma Jobs (2–4 Years Experience)

(DRA Executive Job in Noida 2026)

Introduction

The pharmaceutical industry in India is growing rapidly, especially in regulatory affairs, where skilled professionals are in high demand. If you are looking to build a stable and high-growth career in Drug Regulatory Affairs (DRA), this opportunity for a DRA Executive in Noida is highly valuable.

This role is ideal for candidates with hands-on experience in regulatory documentation, CTD/ACTD dossier preparation, and compliance with Indian regulatory authorities. With increasing drug approvals and global expansion, regulatory professionals are becoming a key part of pharma success.

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🏢 About The Company

This opportunity is offered by a growing pharmaceutical organization focused on regulatory excellence, product compliance, and global expansion strategies. The company operates across multiple therapeutic segments and ensures compliance with strict regulatory standards in India and international markets.

Headquarters: India
Industry: Pharmaceutical / Regulatory Affairs
Founded: Not publicly disclosed
Employees: Estimated 200–500 professionals

The company provides strong exposure to regulatory documentation, dossier submission, and compliance management, making it a good platform for career growth in pharma regulatory affairs.

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📊 Job Overview Summary

The DRA Executive role focuses on managing regulatory submissions, preparing CTD/ACTD dossiers, and ensuring compliance with CDSCO and other regulatory bodies.

You will be responsible for coordinating with internal teams, maintaining documentation, and handling approval processes. This job plays a crucial role in ensuring that pharmaceutical products meet all regulatory requirements before entering the market.

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📌 Vacancy Details

Role: DRA Executive
Location: Noida, Uttar Pradesh, India
Experience: 2–4 Years
Job Type: Full-Time
Industry: Pharmaceutical / Regulatory Affairs

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🔬 Responsibility Explanation

As a DRA Executive, your primary responsibility will be managing regulatory submissions and documentation. You will prepare CTD/ACTD dossiers required for drug approvals and ensure all data is accurate and compliant.

You will work closely with QA, QC, and R&D teams to gather necessary information and ensure smooth submission processes. Tracking approval timelines, responding to regulatory queries, and maintaining audit-ready documentation will also be part of your role.

This position requires strong attention to detail because even small errors in regulatory submissions can delay product approvals.

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🎓 Eligibility Criteria

Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related field
2–4 years of experience in Drug Regulatory Affairs
Knowledge of CTD/ACTD submissions
Familiarity with CDSCO, FSSAI, and AYUSH guidelines

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🧠 Skills Required

To succeed in this regulatory affairs role, candidates should have strong documentation and analytical skills. Understanding of regulatory frameworks and submission formats is essential.

You should be comfortable handling multiple projects, coordinating with different departments, and managing timelines efficiently. Good communication skills are important for interacting with regulatory authorities and internal teams.

Attention to detail, problem-solving ability, and knowledge of compliance standards will give you a strong advantage.

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💰 Salary Estimate

Estimated Salary: ₹3.5 LPA – ₹6.5 LPA

Salary may vary based on experience, company size, and expertise in regulatory submissions. Candidates with exposure to global markets or advanced dossier handling may receive higher packages.

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🎤 Interview Details

The interview process typically includes:

• HR screening
• Technical interview (Regulatory Affairs & CTD knowledge)
• Final discussion with senior management

Shortlisted candidates will be contacted directly by the company.

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📄 Required Documents

Candidates should keep the following documents ready:

• Updated Resume/CV
• Educational Certificates
• Experience Letters
• Salary Slips (if applicable)
• ID Proof

Having proper documentation increases your chances of faster selection.

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❓ FAQs

1. What is the role of a DRA Executive?

A DRA Executive handles regulatory submissions, documentation, and ensures compliance with drug approval authorities.

2. What is CTD/ACTD in pharma?

CTD (Common Technical Document) and ACTD are standardized formats used for regulatory submissions in different countries.

3. Is this job suitable for freshers?

No, this role requires 2–4 years of experience in regulatory affairs.

4. What skills are important for regulatory jobs?

Documentation, regulatory knowledge, attention to detail, and communication skills are essential.

5. What is the career growth in DRA?

You can grow into roles like Regulatory Manager, Global Regulatory Specialist, or Compliance Head.

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✅ Final Conclusion

The DRA Executive job in Noida is a strong opportunity for professionals looking to build a long-term career in pharmaceutical regulatory affairs. With increasing demand for drug approvals and compliance expertise, this field offers stable growth, good salary potential, and global opportunities.

If you have experience in CTD/ACTD submissions and regulatory documentation, this role can significantly boost your career in pharma regulatory affairs.

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📩 How to Apply

Send your updated CV to:

hr4@biodealpharma.com

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⚠️ Disclaimer

Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.

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