Job Description

Nutralike

is a leading nutraceutical manufacturer offering premium-quality products across tablets, capsules, powders, and syrups. With global compliance standards and presence across ROW, Middle East, EU, CIS, and GCC markets, Nutralike focuses on innovation, safety, and quality. Learn more at www.nutralike.com.

Job Summary:

The Regulatory Affairs Executive will be responsible for preparing, reviewing, and submitting regulatory dossiers for nutraceutical products intended for Rest of the World (RoW) markets. The role ensures compliance with country-specific requirements and involves coordination with internal teams, distributors, and regulatory agents for timely approvals.

Key Responsibilities:

Prepare and review CTD/eCTD/non-CTD dossiers for new registrations, renewals, and variations for RoW markets (Africa, CIS, LATAM, Southeast Asia). Coordinate with agents/distributors for submissions, responses, and approvals. Monitor and interpret regulatory changes and keep teams updated. Manage lifecycle documentation including renewals, labeling updates, and post-approval variations. Maintain and update regulatory trackers, databases, and documentation records.

Education:

Bachelor's or Master's degree in

Pharmacy or Life Sciences

.

Must Have Requirements (Top 3):

3-5 years of experience in

Regulatory Affairs

for nutraceutical or pharmaceutical products. Strong knowledge of

CTD/non-CTD dossier formats

and RoW regulatory requirements. Experience coordinating with

agents/distributors

for international submissions.

Good to Have Responsibilities:

Exposure to Middle East, EU, and GCC markets. Excellent communication and document management skills.
Job Type: Full-time

Pay: ₹20,000.00 - ₹50,000.00 per month

Work Location: In person