KORUM by worldhire

QMS Quality Manager

Excelya

Industry
-
Location
Gidy, France
Work mode
hybrid
Job type
-
Annual salary
Not specified
Minimum experience
7+ years
Posted
14th August, 2026

Required skills

Document ManagementChange ManagementQuality AssurancePharmacy

About the role

Join Excelya, a company driven by Audacity, Care, and Energy, where innovation and collaboration are at the heart of everything we do.

As a QMS Quality Manager, you will support a strategic site transformation project by ensuring the successful integration of quality management systems and documentation processes following the transfer of activities to the Gidy site. You will play a key role in document harmonization, training, quality oversight, and change management while ensuring compliance with GMP requirements and project timelines.

Key Responsibilities :

  • Lead the integration of the Quality Management System (QMS), including documentation and training activities related to the transfer of operations.
  • Define and manage documentation scopes associated with transferred activities.
  • Support teams in the drafting, review, and continuous improvement of quality documents, including SOPs, procedures, and forms.
  • Ensure harmonization of documentation practices across impacted sites.
  • Coordinate documentation activities and monitor project timelines to ensure successful delivery.
  • Track action plans, identify risks and bottlenecks, and implement mitigation actions to maintain project milestones.
  • Manage training activities from needs identification through content development, delivery, and effectiveness assessment.
  • Support change management initiatives by facilitating adoption of new processes and addressing resistance to change.
  • Coordinate quality events linked to the project, including Change Controls, CAPAs, and deviations.
  • Develop and monitor project KPIs and maintain quality trackers to ensure project visibility and compliance.
  • Master's degree in Quality Assurance, Life Sciences, Pharmacy, Engineering, or a related field.
  • Strong experience in Quality Management Systems (QMS) within a GMP-regulated environment.
  • Strong knowledge of Quality Management Systems, GMP requirements, CAPA management, Change Controls, and deviations.
  • Experience in document management, SOP creation, and quality documentation review.
  • Proven ability to coordinate cross-functional teams and manage complex projects.
  • Good IT affinity, including Microsoft Office tools and quality management systems.
  • Experience monitoring KPIs and driving quality improvement initiatives.
  • Good level in English.

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