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Amaris Consulting Logo Amaris Consulting · IT - Administration

Msat Quality Lead Pharma

Belgium, Braine-L'alleud · Job Posted June 14, 2026
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Job Description

To support a growing portfolio of pharmaceutical projects and upcoming product launches, we are reinforcing our Pharma MSAT Quality team with an experienced MSAT Quality Lead. You will play a key role in complex technology transfer projects, ensuring supply continuity and providing second-line quality support across both internal and external manufacturing sites. This is a project-driven role with strong potential for extension, depending on project milestones and budget.

Job Responsibility

  • Support technology transfers (process and/or analytical) for Drug Substance (DS), Drug Product (DP), and Packaging
  • Ensure quality oversight during process validation and continuous process verification (CPV)
  • Act as second-line support for complex or cross-site quality issues
  • Provide QA expertise during complex investigations and in the definition and follow-up of CAPAs
  • Challenge and review technical content from an operational QA perspective
  • Participate in cross-functional meetings, ensuring alignment on timelines, risks, and deliverables
  • Maintain close follow-up on project milestones and proactively escalate issues when needed
  • Contribute to quality agreement preparation and review
  • Support vendor-related QA activities
  • Temporarily support other quality teams facing high workload

Requirements

  • Minimum ~5 years of relevant experience in a similar role
  • Strong background in pharmaceutical quality and operations is strongly preferred
  • Able to operate autonomously, take part in complex technical and quality discussions, and act with limited supervision
  • Strong Quality mindset with a solid understanding of pharmaceutical regulations (GMP and related guidelines)
  • Proven experience in technology transfer (process and/or analytical), ideally in a QA context
  • Operational QA experience with the ability to understand, challenge, and defend technical content
  • Hands-on experience with complex investigations, deviation management, and CAPA lifecycle
  • Excellent communication skills in English (written and verbal)
  • Ability to work independently in a cross-functional, international, and multicultural environment

Nice to have

  • Experience in both process and analytical domains
  • Exposure to different formulations and stages: DS, DP, and packaging
  • French language skills
  • Experience in biologics and/or non-pharma industries, provided the quality and tech transfer mindset is strong
  • Previous experience working in global or multicultural teams
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