Chennai Tamil Nadu Regulatory affairs Jobs – 10 Open Jobs Today

Regulatory Affairs Executive
Regenix Biosciences Ltd —Chengalpattu, Chennai, Tamil Nadu
- ₹21,000 - ₹30,000 a month
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Regulatory Affairs
Pharm Products —Chennai, Tamil Nadu
- Master's degree
Executive & Sr. Executive – Analytical Research & Development (Review)
Axxelent Pharma and Science Private Limited —Tharamani, Chennai, Tamil Nadu
- ₹2,60,000.00 - ₹12,31,916.17 a year
- Full-time
- Research
- Master's degree
- Analysis skills
- Flexible schedule
- Food provided
Quick apply
9d
Manager - RegCMC, Medical Devices
Pfizer —Chennai, Tamil Nadu
- Full-time
- Hybrid work
- Computer literacy
- Microsoft Office
- Project management
17h
Lead, Global Complaint Management
ICU Medical, Inc. —Chennai, Tamil Nadu
- Full-time
- Microsoft Powerpoint
- Nursing
- Microsoft Outlook
Business Partner – Regulatory Operations
Navitas Life Sciences —Chennai, Tamil Nadu
- Full-time
- Bachelor's degree
- Communication skills
Senior Manager - Bio Analytical
KMS health center pvt ltd —Chennai, Tamil Nadu
- ₹90,000 - ₹2,00,000 a month
- Full-time
- Management
- Master's degree
- Project management
Quick apply
Sr Clinical Research Supv
Medtronic —Chennai, Tamil Nadu
- Full-time
- Management
- Bachelor's degree
3d
Business Development Associate – Pharmaceutical Industry
Resolute Enterprises —Chennai, Tamil Nadu
- ₹12,000 - ₹30,000 a month
- Full-time
- Sales
- Business development
- Project management
Quick apply
14d

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Regulatory Affairs Executive

Regenix Biosciences Ltd -
Chengalpattu, Chennai, Tamil Nadu

Quick apply

Job details

Permanent | Full-time
₹21,000 - ₹30,000 a month

Benefits

Provident Fund

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Windows
Microsoft Office
Bachelor's degree
Organisational skills
Communication skills

Full job description

Job Title: Regulatory Affairs Executive / Senior Executive
Department: Regulatory Affairs
Experience: 2–5 Years
Qualification: B.Pharm / M.Pharm
Industry: Pharmaceutical – Sterile Formulations (Parenteral / Injectable / Biological Products)

Job Summary

We are looking for a Regulatory Affairs professional with 2–5 years of experience in the pharmaceutical industry. The ideal candidate should have experience in regulatory submissions for Parenteral, Injectable, and Biological products, handling RoW and CDSCO markets, and managing various online regulatory portals to ensure timely approvals and regulatory compliance.

Key Responsibilities

Prepare, review, compile, and submit regulatory dossiers for RoW markets and CDSCO.
Handle new product registrations, renewals, variations, amendments, and post-approval lifecycle activities.
Prepare and review CTD/eCTD dossiers and responses to regulatory authority queries.
Coordinate with R&D, QA, QC, Production, Packaging Development, and other cross-functional teams for regulatory documentation.
Ensure compliance with CDSCO, ICH, WHO, and country-specific regulatory requirements.
Maintain regulatory submission trackers, product registration databases, and document repositories.
Review product labels, artworks, package inserts, and promotional materials for regulatory compliance.
Support change control assessments and regulatory impact evaluations.
Monitor regulatory timelines and ensure timely submissions and approvals.

Online Regulatory Portal Management

Handle online applications and submissions through regulatory portals, including:
ONDLS (Online National Drugs Licensing System)
NSWS (National Single Window System)
TNSWP (Tamil Nadu Single Window Portal)
CDSCO SUGAM Portal / CDSCO Online Portal
Upload, track, and monitor applications, approvals, licenses, and renewals.
Coordinate with regulatory authorities for online queries, clarifications, and application status updates.
Maintain digital records of submissions and regulatory approvals.

Required Skills

Strong knowledge of CDSCO regulations and RoW registration requirements.
Experience in handling Parenteral, Injectable, and Biological products.
Hands-on experience in CTD/eCTD dossier compilation and lifecycle management.
Experience in handling ONDLS, NSWS, TNSWP, and CDSCO Online/SUGAM portals.
Knowledge of ICH, WHO, and global regulatory guidelines.
Excellent documentation, communication, and coordination skills.
Proficiency in Microsoft Office (Word, Excel, PowerPoint).

Educational Qualification

B.Pharm / M.Pharm

Experience

2–5 years of experience in the Regulatory Affairs department of a pharmaceutical company.

Product Exposure

Parenteral Products
Injectable Products
Biological Products

Market Exposure

CDSCO (India)
RoW (Rest of World) Markets

Preferred Candidate Profile

Experience in handling online regulatory applications and licensing processes.
Ability to coordinate with regulatory authorities and internal stakeholders for timely approvals.
Strong organizational skills with the ability to manage multiple regulatory projects simultaneously.
Knowledge of regulatory lifecycle management, change control, and post-approval submissions.

Pay: ₹21,000.00 - ₹30,000.00 per month

Benefits:

Provident Fund

Work Location: In person

Quick apply

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