PpOur 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. /p ul liYou possess a Master’s degree in a scientific field. /li liYou bring 8+ years of experience in bQA /b oversight within a bGMP /b manufacturing environment. /li liYou have a proven track record in health authority inspections and the certification process for new manufacturing facilities. /li liYou possess strong knowledge of bbiopharmaceuticals /b or bgene therapy /b manufacturing processes. /li liYou bring expertise in bGMP /b, bCFR /b, and bEudralex /b regulations for biopharmaceutical manufacturing. /li liYou're able to provide mature quality judgment and communicate effectively with senior stakeholders. /li liYou are fluent in bEnglish /b and bFrench /b. /li /ul h3Nice to Have /h3 ul liBroad transversal QA experience across multiple domains. /li liAbility to adapt to evolving priorities in an inspection-driven environment. /li /ul /p #J-18808-Ljbffr