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 technical files meet the stringent requirements of international partner companies. Core Responsibilities & Technical Scope Standard Core Responsibil...