Job Description

Job Title: IRA - Export Documentation Executive

Location:

Vatva GIDC

Experience:

0 to 3 Years

Industry:

Pharmaceutical

Key Responsibilities

Prepare and manage

export regulatory documents

as per international requirements. Compile and maintain

product dossiers

for export registrations. Coordinate with

Production, QA, and QC departments

to collect required documents for dossier preparation. Follow up on

regulatory samples

required for product registration. Prepare

draft labels

for export product permission applications. Prepare and review

Package Inserts (PIs)

for export products. Coordinate with the

Regulatory Affairs (RA) department

for permissions, COPP, FSC, and other regulatory certificates. Maintain and track

export orders and regulatory status.

Coordinate with the

Production Department on a weekly basis

to ensure regulatory alignment. Prepare and compile regulatory reports and documents such as

SPEC, MOA, MFR, Stability Data, and related records.

Required Skills & Competencies

Basic to good knowledge of international regulatory affairs and export documentation Strong coordination and follow-up skills Attention to detail and documentation accuracy Ability to work cross-functionally with multiple departments
Job Type: Full-time

Pay: ?20,000.00 - ?25,000.00 per month

Work Location: In person