Contracting – Brabant Wallon Identical to USP QA Officer, but here we focused on Downstream processes such as purification, chromatography, UF, etc: Review paper and electronic batch records line by line. Validate data entries, timestamps, and operator actions. Ensure deviations and alarms are properly documented. Conduct field checks (logbooks, IT systems). Collaborate with production and compliance teams. Support training and coaching of operators on deviation initiation. Minimum 5 years of experience, with strong production experience. Experience in pharma is a must. Experience in Downstream biomanufacturing. Batch record and deviation review expertise. Production background (Quality profile who has worked in production quality). French fluency. On-site availability. Proactive and communicative personality. Nice to have: English proficiency. QA experience in production. Ability to coach operators. Jefferson Wells offers you a permanent cont... Expertise, VOS, Accurate Data Entry, Use ICT systems, Proactivity, Chromatography, Production, Timestamp, Downstream, Checks, Coaching, Quality assurance, Alarms, Logbooks, Batch Records, Training Originele vacature is te vinden op StepStone.be – Maak nu een Jobagent aan op StepStone en vind je droombaan! https://bit.ly/2jPYsZC Vind gelijkaardige jobs, informatie over werkgevers en carrièretips op StepStone.be!
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