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Qc equipment specialist

Braine-l'Alleud
Ucb Pharma
Publiée le 17 juin
Mission du poste

Make your mark for patients

We are looking for a QC Equipment Specialist who is collaborative, proactive, and quality-driven to join our Quality Control Microbiology & Environmental Monitoring team, based at our UCB campus located in Braine-l’Alleud, Belgium.

About the role

You will play a key role in strengthening our microbiology laboratory capabilities and ensuring regulatory compliance across microbiology activities. You are going to support laboratory operations, introduce new technologies, improve testing efficiency, and help teams deliver reliable, compliant, and high-quality results. You will also contribute to major change projects, training initiatives, and the implementation of new production facilities.

Who you will work with

You will work closely with the QC Microbiology laboratory, Environmental Monitoring team leaders, technicians, Regulatory Affairs, Quality Assurance, development teams, and other site stakeholders. You are going to collaborate in a matrix environment where teamwork, scientific expertise, and operational excellence are essential to support laboratory performance and manufacturing needs.

What you will do

  • You will evaluate, introduce, and implement new laboratory equipment and microbiology technologies.
  • You will be responsible for equipment availability, maintenance follow-up, and laboratory readiness based on workload and priorities.
  • You will support microbiology method development, validation, and technology transfer to improve QC efficiency.
  • You will manage regulatory microbiology topics and ensure compliance with evolving regulatory requirements.
  • You will support sampling plans for products, environments, and utilities with team leaders and stakeholders.
  • You will train technicians, support troubleshooting, and drive continuous improvement and major change projects.
  • Interested? For this role, we are looking for the following education, experience, and skills:

  • Master’s degree in microbiology, life sciences, pharmacy, or a related scientific field.
  • Experience in microbiology laboratory operations within a regulated pharmaceutical or biotech environment.
  • Strong knowledge of GMP, laboratory compliance, audits, deviations, CAPAs, and regulatory expectations.
  • Ability to lead projects, manage change, and support laboratory and manufacturing investigations.
  • Strong communication skills in English and French with diverse technical and business stakeholders.
  • People-oriented mindset with coaching ability, sound judgment, and a proactive problem-solving approach.
  • Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

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