Regulatory Affairs Executive

GSS Pharma Pvt.ltd; Bengaluru; On-site; INR 600,000 - 800,000; Full time

Job summary

GSS Pharma Pvt.ltd in Bengaluru is seeking a Regulatory Affairs Executive with 1–3 years of experience in the pharmaceutical industry to support regulatory submissions.

The role focuses on compiling and reviewing ACTD and CTD dossiers, maintaining regulatory documentation, coordinating with cross-functional teams, and ensuring timely submissions while adhering to regional guidelines.

Qualifications

• 1–3 years of experience in pharmaceutical regulatory affairs.
• Hands-on experience in compiling and reviewing ACTD and CTD dossiers for regulatory submissions.
• Knowledge of regulatory guidelines and submission processes.

Responsibilities

• Preparing, compiling, and maintaining regulatory documentation in accordance with regional requirements.
• Coordinating with cross-functional teams to gather necessary data.
• Ensuring timely submission of dossiers.
• Handling multiple projects simultaneously as needed.

Skills

ACTD/CTD dossiers

Regulatory submissions

Cross-functional coordination

Regulatory guidelines

Job description

We are seeking a Regulatory Affairs Executive with 1 to 3 years of experience in the pharmaceutical industry.

The ideal candidate should have hands‑on experience in compiling and reviewing ACTD and CTD dossiers for various regulatory submissions.

Responsibilities include preparing, compiling, and maintaining regulatory documentation in accordance with regional requirements, coordinating with cross-functional teams to gather necessary data, and ensuring timely submission of dossiers.

The candidate should be well‑versed with regulatory guidelines, and capable of handling multiple projects simultaneously.