水平: Associate

工作类型: Full-time

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工作内容

Your role will be to
  • Assist in the batch release process, ensuring on time release in compliance with regulatory and GxP-requirements
  • Evaluate product quality complaints.
  • Manage complaint samples. ; Follow-up and review the complaint investigations performed by the manufacturers. Perform complaint trending and reconciliations,
  • Tracking and coordinating repacking activities,
  • Support the QA team with the development and maintenance of procedures and work instructions,
  • Support the management of Change Controls by assisting in the initiation, follow-up and action plan execution of Change Controls,
  • Assist in the GxP-inspection readiness process and provide support during audits and inspections of the organization,
  • Support / facilitate local deviation investigations (Root Cause Analysis) and CAPA determination and execution,
  • Contribute to the Area Quality Plan and ensure that agreed actions are locally executed,
  • Administrative support in preparing reviews and KPI-reporting,
  • Assist with Periodic Reviews (PR),
  • Organize / prepare local training and on-boarding activities,
  • Management of quality documentation (retention, archiving),
  • Support in the maintenance of Quality Agreements with suppliers.
Your profile
  • A University Master’s degree in a relevant scientific subject (bioscience, chemistry, pharmacy, healthcare, ...),
  • A high professional level of English and fluent in French,
  • At least a first thorough QA experience in a GMP environment,
  • Mobility towards at least one of our major clients located in Lessines, Braine-L’alleud, Wavre, Rixensart, Gosselies,
  • Analytical mind, good attention to detail and problem solving skills within a structured process,
  • Good team player – works well in cross-functional teams,
  • Works with a spirit of continuous improvement and innovation, creatively open to new ideas and methods.
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最后期限: 18-12-2025

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