Manager – Global Regulatory Affairs

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

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7fb7vz