/ L'annuaire des offres d'emploi en Suisse Romande
n/a n/a Geneva CH
full-time

Specialist, Pharmaceutical Products, Quality Assurance

Entreprise
Experis
Lieu
Geneva
Date de publication
08.05.2026
Référence
5231497

Description

Experis® is a global leader in IT professional resourcing, permanent recruitm
Specialist, Pharmaceutical Products, Quality Assurance
Experis® is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers.
Specialist, Pharmaceutical Products, Quality Assurance
Experis® is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers.
Specialist, Pharmaceutical Products - Quality Assurance (Interim)
About the role: We're recruiting for an experienced pharmaceutical QA specialist to join our Clients Supply Operations team on an interim basis. You will help ensure that pharmaceutical products procured through global health programmes meet quality, safety and efficacy standards, working across policy, risk management, partner engagement and grant implementation support.
Key responsibilities
Lead investigations of quality complaints, safety events and out-of-specification findings, advising on risk mitigation
Provide QA guidance and support to internal teams on pharmaceutical product eligibility and compliance
Manage the Expert Review Panel (ERP) secretariat process in collaboration with WHO
Maintain and update product master data and eligibility lists
Contribute to QA policy development, tools and guidance
Engage with WHO, regulatory authorities and international procurement agencies on QA harmonisation
Support cross-functional collaboration across supply operations, grant management and technical teams
Essential requirements
Advanced degree in pharmacy, laboratory science, or biomedical/chemical engineering
Minimum 5 years' experience in pharmaceutical products QA, risk management and regulatory affairs
Experience working with UN agencies, international NGOs or donors on QA matters
Track record managing complex QA issues at country, regional or international level
Experience developing QA policies, tools and guidance
Fluent English
7+ years in pharmaceutical design and manufacturing
Experience with a major multilateral organisation
Project management or process improvement qualifications
Working knowledge of French
For this position we can only consider applicants with a Swiss work permit or a Swiss/EU passport. jid8026997afr jit0521afr jpiy26afr

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