As we scale our manufacturing footprint including our expansion into the

AMTZ

and our new pharmaceutical facility the regulatory landscape is our most critical strategic pillar. We are seeking a

Deputy Head of Regulatory Affairs

to lead the complex task of harmonizing international standards across our proprietary brands and our

OBL/White Label partnerships .

Key Result Areas (KRAs)
Market Access & Timelines:

Achieve 100% on-time submission and approval of regulatory dossiers for new product launches.
Audit & Recall Readiness:

Maintain a Zero Critical Non-Conformance status during audits and ensure the

Global Recall System

is well-oiled and capable of immediate execution.
Clinical & Scientific Authority:

Oversee the successful completion of clinical trials data to support

EU MDR

requirements.
Partner Compliance:

Ensure all

OBL/White Label