Description

Senior Quality executive and Swissmedic-accredited Qualified Person / Responsible Person with 15+ years leading quality organizations within global pharmaceutical and life sciences environments. Proven expertise in GMP/GDP compliant Quality Management Systems, leading 10+ audits per year as Lead Auditor across manufacturing sites, CMOs and distribution partners, and driving supply chain and laboratory optimization initiatives. Co-founder of a pharmaceutical quality & regulatory consulting group, with experience spanning Switzerland, France, EU and MENA markets. Instructor at the University of Geneva (Doctorate in Pharmaceutical Sciences, CAS in Quality in the Pharmaceutical Industry).

Industry field of expertise

Languages

French
Native or bilingual
English
Native or bilingual
Arabic
Fluent

Workplace preferences

Can work on-site

Genève (up to 50km)

EMNA Group
Co-Founder & Managing Director
PHARMACEUTICALS INDUSTRY
September 2025 - Today (11 months)
Geneva, Switzerland
• • Co-founded a pharmaceutical quality & regulatory consulting group (Switzerland,
France, North Africa)
• • Lead Auditor for GMP/GDP audits across sterile/biotech, solid dosage and API sites
• • Provide outsourced QP/RP services for pharmaceutical and MedTech clients
• • Developing SwissMedTrade, the group's international trade division (Swissmedic Art. 18 LPTh licence)
• • Build commercial strategy, training catalogue and market partnerships
Formation Commerce international Audit Conseil Management de la qualité
Hikma Pharmaceuticals
Responsible Person
PHARMACEUTICALS INDUSTRY
September 2025 - Today (11 months)
Geneva, Switzerland
• Built and implemented the GDP Quality Management System from scratch for Swiss operations
• Oversight of distribution activities and external logistics partners
• Ensure Swissmedic inspection readiness and regulatory compliance
Conformité réglementaire Management de la qualité QP Gestion de projet freelance
LABATEC Pharma
Head of Quality ,Responsible Person
January 2024 - May 2026 (2 years and 4 months)
Geneva, Switzerland
• • Member of the executive committee reporting to the CEO
• • Lead global quality operations across multiple regions and external partners
• • Responsible for QMS governance and batch release for Swiss and MENA markets
• • Lead and conduct internal, external and supplier audits (GMP/GDP/GVP spanning sterile/biotech sites, oral solid dosage plants, semi-solid manufacturing and API suppliers
• • Oversee regulatory submissions, pharmacovigilance compliance and quality strategy