Packaging Deviations Specialist

Packaging Deviation & Continuous Improvement Specialist Brussels, Belgium About Nalys Nalys 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 Role For 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 Responsibilities Draft and investigate deviations, discrepancies, complaints, and loss‐of‐efficiency cases Write, implement, and track CAPA's linked to deviations or audit outcomes Prepare and update procedures and draft Change Controls Execute and follow up on change control‐related tasks Perform root‐cause analyses while ensuring strict adherence to GMP and internal procedures Improve existing processes and contribute to technical and operational optimization projects Participate in cost‐reduction initiatives and yield‐improvement projects Train Packaging teams on new procedures, deviations, and change control management Support performance monitoring through Packaging Support KPIs Participate in client visits, audits, technical meetings, and new product introductions when required. Your Profile You hold an Engineer degree, master's degree, or equivalent by experience You are an expert in one or more pharmaceutical activities: Production, Engineering, QA, or QC You have a strong knowledge of GMP standards and Quality Management Systems Experienced in problem‐solving and project management You have an analytical mindset and structured approach to investigations Good understanding of safety requirements and quality procedures You are a good communicator, with cross‐functional collaboration skills You are fluent in both French and English. What We Offer at Nalys A long‐term consultancy assignment within a reputable global pharmaceutical manufacturer A stimulating environment that values expertise, innovation, and continuous improvement A supportive team, training opportunities, and a culture focused on personal and professional development. Recruitment Process At 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 screening A second interview will be held with one of our technical experts Final 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.