Leadership Tempo pieno Onsite

Experience Required

7.0 - 10.0 Years

Job Description

The Global Regulatory Affairs Lead is responsible for end-to-end product registrations and regulatory strategy across multiple geographies.

This role ensures that all Taevas products meet country-specific regulatory requirements and are approved for market entry in a timely and compliant manner.

Key Responsibilities

Global Product Registrations
Lead regulatory submissions across key markets (India, US, EU, UAE, LATAM, APAC, etc.).
Prepare and submit dossiers (CDSCO, US FDA, CE/MDR, MOHAP, PMDA, COFEPRIS, etc.).
Manage technical documentation (Technical File, STED, DMF, CER, etc.).
Track approvals, renewals, and post-market variations.
Regulatory Strategy
Define registration pathways for new products and markets.
Provide regulatory feasibility inputs during product selection / OEM onboarding.




Optimize timelines and cost for registrations globally.
Stakeholder & Agency Management
Liaise with Notified Bodies, regulatory consultants, labs, and local agents.
Coordinate with international partners for country-specific approvals.
Labeling & Compliance
Ensure compliance for labeling, IFUs, UDI, packaging requirements.
Align regulatory documentation with market-specific requirements.

Preferred Profile

6–12+ years in medical device regulatory affairs
Experience in multi-country registrations
Exposure to US FDA, CE/MDR, CDSCO
Strong documentation & coordination skills
Experience in a medical device manufacturing company (preferred)

Application Deadline

07/31/2026

📌 Manager – Global Regulatory Affairs (Monteviale)
🏢 Taevas Life Sciences
📍 Monteviale