Packaging Deviations Specialist

il y a 1 jour


Brussels, Belgique Nalys Temps plein

Packaging Deviation & Continuous Improvement Specialist Brussels, BelgiumAbout NalysNalys is a fast‐growing consultancy company specialised in high‐tech engineering and life sciences. We partner with industry leaders to deliver expert support, innovative solutions, and high‐value technical capabilities. Joining Nalys means becoming part of a dynamic, people‐driven organisation that values excellence, continuous learning, and collaboration. Together, we help our clients create safer, more efficient, and more innovative healthcare solutions.About the RoleFor one of our key pharma partners, we are looking for a Packaging Deviation & Continuous Improvement Specialist to support the Packaging department's operational performance.In this role, you will drive the investigation, documentation, and continuous improvement activities related to deviations, CAPA, change controls, and quality events within a highly regulated GMP packaging environment. You will collaborate closely with internal teams to enhance process reliability, product quality, and operational excellence.Key ResponsibilitiesDraft and investigate deviations, discrepancies, complaints, and loss‐of‐efficiency casesWrite, implement, and track CAPA's linked to deviations or audit outcomesPrepare and update procedures and draft Change ControlsExecute and follow up on change control‐related tasksPerform root‐cause analyses while ensuring strict adherence to GMP and internal proceduresImprove existing processes and contribute to technical and operational optimization projectsParticipate in cost‐reduction initiatives and yield‐improvement projectsTrain Packaging teams on new procedures, deviations, and change control managementSupport performance monitoring through Packaging Support KPIsParticipate in client visits, audits, technical meetings, and new product introductions when required.Your ProfileYou hold an Engineer degree, master's degree, or equivalent by experienceYou are an expert in one or more pharmaceutical activities: Production, Engineering, QA, or QCYou have a strong knowledge of GMP standards and Quality Management SystemsExperienced in problem‐solving and project managementYou have an analytical mindset and structured approach to investigationsGood understanding of safety requirements and quality proceduresYou are a good communicator, with cross‐functional collaboration skillsYou are fluent in both French and English.What We Offer at NalysA long‐term consultancy assignment within a reputable global pharmaceutical manufacturerA stimulating environment that values expertise, innovation, and continuous improvementA supportive team, training opportunities, and a culture focused on personal and professional development.Recruitment ProcessAt Nalys, our hiring process is designed to be transparent and engaging:Olivia Braszko, TA Specialist at Nalys, will review your application and schedule an initial screeningA second interview will be held with one of our technical expertsFinal interview with our Business Unit Director, Jimmy Rousseaux.Ready to make an impact?If you are passionate about quality, operational excellence, and supporting pharmaceutical manufacturing teams, we'd love to meet you Apply now and join the Nalys community.



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