Deviation Writer 📍Brabant wallon, BelgiumIntroductionNalys is a Belgian recruitment and consultancy firm specialised in the pharmaceutical, biotech and life sciences industries. With deep expertise across quality, manufacturing and engineering development, we support both large international groups and innovative scale-ups in building the teams that drive their projects forward. When we place a professional, we stay by their side — before, during and after the mission.Today, we're looking for an experienced Deviation Writer to provide focused, autonomous support within a biologics production environment in the Brabant wallon area. This is a 100% deviation management role — created specifically to absorb a significant backlog of DSP production deviations. You'll be operational from day one, with real impact and full ownership of your scope.Your ResponsibilitiesAs the new Deviations Writer, you will will :Own end-to-end management of DSP production deviations — from initial detection through to closure in the Quality SystemConduct field investigations directly in production areas — interviewing technicians, observing equipment and understanding processes in contextWrite deviations of all types — minor, major and clustered — with precision, structure and full GMP complianceParticipate actively in root cause analyses and defend your technical conclusions with QACoordinate closely with Production, QA, QA Validation, MSAT/QAMSAT and Maintenance & Technical ServicesMaintain a target pace of deviations closed per week, across a mixed minor/major portfolioProactively gather information without waiting to be guided — autonomy is essential from the start.Your ProfileYou have a first proven experience in production deviation writing — QC-only profiles are not suitable for this roleYou have background in industrial-scale manufacturing environments, ideally in biologics or biopharmaDSP knowledge or experience is a strong assetYou feel comfortable to act autonomously — limited coaching will be available; you must be able to drive your own workloadYou also feel comfortable working in production areas and on the shop floor, able to interact with, challenge and convince both QA and Production stakeholdersFluent French is mandatory — Intermediate English required for reading documentation, occasional writing and stakeholder interactionsWhat We OfferA human‑scaled consulting company focused on expertise, partnership, and career developmentLong‑term assignments with leading pharmaceutical playersContinuous learning through technical coaching, training, and knowledge sharingA supportive culture that values autonomy, trust, and impactAn attractive salary package with additional benefits.Our Recruitment ProcessWhen applying for this position at Nalys, you can expect a clear and engaging recruitment journey:Talent Acquisition CallA first discussion with our Talent Acquisition Specialist, Olivia Braszko, to understand your background, motivations, and career goalsTechnical InterviewA meeting with one of our Technical Referent to evaluate your expertise and fit for the missionBusiness InterviewA conversation with the Business Unit Director, Jimmy Rousseaux, to discuss the project context and your future within Nalys.Interested?👉 Apply directly via this post and let's discuss your motivation through a first teams meeting!