Our client, a leading pharmaceutical company, is seeking a specialist to oversee the qualification and operational readiness of a new production facility. The role involves partnering with project stakeholders to establish robust quality oversight throughout the transition from design to routine manufacturing operations.
You possess a Master’s degree in a scientific field.
You bring 8+ years of experience in QA oversight within a GMP manufacturing environment.
You have a proven track record in health authority inspections and the certification process for new manufacturing facilities.
You possess strong knowledge of biopharmaceuticals or gene therapy manufacturing processes.
You bring expertise in GMP, CFR, and Eudralex regulations for biopharmaceutical manufacturing.
You're able to provide mature quality judgment and communicate effectively with senior stakeholders.
You are fluent in English and French .
Nice to Have
Broad transversal QA experience across multiple domains.
Ability to adapt to evolving priorities in an inspection-driven environment.
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