Cureton Biotech Regulatory Affairs Jobs

Cureton Biotech Hiring Regulatory Affairs Executive in Delhi | Pharma Export Jobs 3–6 Years Experience

A high-value opportunity is now open for experienced regulatory affairs professionals in the pharmaceutical export domain. Cureton Biotech is hiring a Regulatory Affairs Executive in Delhi for its pharma export and global registration team.

This role is ideal for candidates with 3–6 years of experience in regulatory affairs, especially those with hands-on exposure to CTD/ACTD dossier preparation and international markets such as LATAM and ROW countries.

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Company Overview

Cureton Biotech Pvt. Ltd. is a well-established pharmaceutical company in India, recognized for its commitment to quality and regulatory excellence. The company operates under ISO 9001:2008 certification and adheres to global standards such as GMP, WHO, and GLP.

With a strong focus on pharmaceutical exports, product quality, and regulatory compliance, Cureton Biotech has built a reputation for delivering reliable healthcare solutions across international markets.

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Job Role & Responsibilities

As a Regulatory Affairs Executive, you will handle end-to-end regulatory submissions, export documentation, and compliance activities for global pharmaceutical markets.

Core Responsibilities

• Prepare, review, and submit CTD/ACTD dossiers for international regulatory approvals
• Manage product registrations, export licenses, renewals, and variations
• Coordinate with CDSCO, State FDA, and global regulatory authorities
• Ensure compliance with importing country regulations for pharmaceutical products

Documentation & Compliance

• Handle export documentation including COA, COPP, FSC, and stability data
• Respond to regulatory queries and deficiency letters
• Maintain updated regulatory records and submission timelines
• Support audits, inspections, and documentation reviews

Cross-Functional Coordination

• Collaborate with QA, Production, Logistics, and Marketing teams
• Ensure alignment of regulatory strategy with business and export goals
• Monitor timelines for submission and approval of export consignments

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Eligibility / Qualifications

Educational Background:

B.Pharmacy, M.Pharmacy, Pharmaceutical Sciences, Regulatory Affairs, Life Sciences

Experience Required:

• 3–6 years of experience in pharmaceutical regulatory affairs
• Mandatory experience in CTD/ACTD dossier preparation
• Exposure to LATAM and ROW markets preferred

Skills Required:

• Strong knowledge of global regulatory guidelines (CDSCO, FDA, international markets)
• Expertise in pharmaceutical export documentation and compliance
• Excellent communication and documentation skills
• Ability to manage multiple regulatory submissions and timelines

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Location & Salary

• Location: Okhla Industrial Area Phase 1, New Delhi
• Job Type: Full-time (On-site)
• Salary: ₹40,000 – ₹55,000 per month

Application Process

Interested candidates can apply via:

Email: hr.curetonbiotech@gmail.com

Candidates can also apply through LinkedIn job posting.

Early application is recommended due to competitive hiring in regulatory affairs roles.

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Frequently Asked Questions (FAQs)

1. Is this role suitable for freshers?

No, this role requires 3–6 years of regulatory affairs experience.

2. What is the key requirement for this role?

Hands-on experience in CTD/ACTD dossier preparation.

3. Which markets are preferred?

LATAM and ROW markets experience is preferred.

4. What career growth can I expect?

You can grow into roles like Regulatory Affairs Manager, Global Regulatory Lead, or Export Compliance Head.

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Summary

Category	Details
Company	Cureton Biotech
Vacancies	Regulatory Affairs Executive
Required Education	B.Pharmacy, M.Pharmacy
Experience	3–6 Years

Tagged as: Pharma Jobs in Delhi