Key Responsibilities

  • Lead and manage the integration of quality management systems, certifications, and regulatory requirements into the Global Quality Management System.

  • Ensure continuity of critical quality processes throughout integration phases, minimizing operational disruption.

  • Identify integration-related quality and compliance risks and define effective mitigation strategies to protect product quality and supply continuity.

  • Support and contribute to change management activities associated with acquisitions, system implementations, or organizational transformations.

  • Collaborate cross-functionally with Quality, Regulatory, IT, Operations, and Business stakeholders to ensure alignment with corporate quality standards.

  • Support audit readiness activities, including internal audits, regulatory inspections, and certification processes during and post-integration.

  • Monitor progress, track risks, and report on integration milestones to relevant stakeholders.

  • Ensure alignment with international quality standards and applicable regulatory frameworks

Required Education

  • Bachelor’s degree in Quality, Life Sciences, or a related discipline

  • Master’s degree preferred

Required Experience

Minimum 4 years of experience in Quality Assurance or Quality Systems roles within a regulated environment (e.g., pharmaceutical, biotech, medical devices, or life sciences).

Required Languages

  • English (mandatory)

  • French (preferred)

Required Technical Skills

  • Strong project management and organizational skills.

  • Solid understanding of international quality standards and regulatory frameworks.

  • Experience supporting audits, inspections, and certification activities.

Publish Date

07 January, 2026

Spontaneous Application

Quality Integration Manager - VAF 489

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