Back to search

Specialist QA Monitoring and Market Surveillance

Geneva Interim View Job Description
Our client is seeking a Specialist QA Monitoring, Vigilance & Market Surveillance to strengthen quality assurance, vigilance, and market surveillance activities across complex healthcare supply chains. The role focuses on risk assessment, quality and safety signal analysis, incident management, regulatory collaboration, and the implementation of effective market surveillance strategies.

Added 13/10/2026

  • Drive quality and patient safety initiatives across public health programs.
  • Influence market surveillance strategies that improve access to safe healthcare.

About Our Client

Our client is a leading international organization operating in the global health sector. Through large-scale procurement and supply chain programs, it works to improve access to quality-assured healthcare products and strengthen public health systems worldwide.

Job Description

  • Contribute to the development and enhancement of quality assurance policies, guidelines, and governance frameworks.
  • Provide technical advice and support throughout program design and implementation phases.
  • Analyze quality, safety, efficacy, and product performance signals to identify emerging risks.
  • Lead investigations related to product quality complaints, safety events, and non-conformities.
  • Develop and support market surveillance and vigilance strategies aligned with identified risks.
  • Coordinate product recalls and corrective actions with regulatory authorities and internal stakeholders.
  • Support quality assurance compliance monitoring activities and supplier oversight initiatives.
  • Contribute to country capacity building through training, regulatory strengthening, and vigilance system development.
  • Assess downstream quality assurance risks and recommend mitigation measures.
  • Collaborate with cross-functional teams and external partners to ensure alignment on quality and risk management priorities.
  • Support the development of quality management systems, analytics, performance monitoring, and KPI reporting.



The Successful Applicant

  • University degree in Pharmacy, Chemical Engineering, Life Sciences, or a related discipline.
  • Minimum 5 years of experience in Quality Assurance, Quality Management, or Regulatory Affairs.
  • Proven experience in developing and implementing market surveillance and vigilance programs.
  • Strong understanding of healthcare product quality, safety, and regulatory compliance requirements.
  • Experience working within global public health regulatory environments.
  • Demonstrated ability to manage investigations, risk assessments, and corrective action plans.
  • Experience engaging with international stakeholders, NGOs, donors, regulatory bodies, or multilateral organizations.
  • Strong project management and cross-functional collaboration skills.
  • Ability to analyze complex data sets and identify quality and safety trends.
  • Excellent communication and stakeholder management capabilities.
  • Fluent English; French or additional languages are considered an asset.
  • Knowledge of medical vigilance, pharmacoepidemiology, or relevant ISO standards would be advantageous.



What's on Offer

  • Opportunity to contribute to high-impact global health and patient safety initiatives.
  • International and collaborative environment with diverse stakeholders and experts.
  • Exposure to complex quality assurance, vigilance, and regulatory challenges on a global scale.



Quote job ref
JN-102026-7124904

Job summary

Job Function
Engineering & Manufacturing
Specialisation
Quality
Industry
Public Sector
Where
Geneva
Contract Type
Interim
Job Reference
JN-102026-7124904

Michael Page is an equal opportunity employer committed to workforce diversity, both as an employer as well as a recruitment service provider. Each recruitment decision we make for people we hire and people we place into new roles is based solely on the candidates’ knowledge, experience and skills.