Technical Quality Specialist (Deviation)
All potential applicants are encouraged to scroll through and read the complete job description before applying.Walloon Brabant, BelgiumIntroductionAt Nalys, we are passionate about engineering, technology, and life sciences. As a fast‐growing consultancy company, we support leading pharmaceutical organizations across Europe by providing high‐value technical expertise and a human‐centered approach.For one of our trusted partners in the Brussels area, we are looking for a Technical Quality Specialist to strengthen technical quality activities within a GMP‐regulated environment. This role offers a great opportunity to contribute to meaningful quality processes while growing within a dynamic and supportive engineering community.ResponsibilitiesAs the new Technical Quality Specialist, you will have to :Manage technical deviations from initiation to closure, ensuring timely and compliant documentationSupport CAPA and Change Control processes linked to technical, maintenance, and engineering activitiesCreate, review, and update quality documentation (SOPs, work instructions, forms, checklists)Provide administrative and quality support to technical teams, including supplier requests, purchase coordination, and documentation archivingPrepare and consolidate KPIs related to quality, safety, performance, and technical activitiesContribute to internal and external audits by ensuring accurate and compliant documentationCollaborate with cross‐functional teams such as Quality, Production, Engineering, Maintenance, Purchasing, and HSE.You ProfileYou hold a Degree in a technical, scientific, or pharmaceutical fieldYou have minimum 2 years of experience in a GMP/ISO‐regulated environment (pharma, biotech, medical devices...)You Demonstrate experience managing deviations, CAPA, and quality documentationYou act as a specialist of MS Office usage; experience with TrackWise, EDMS, SAP, or similar tools is a strong assetYou are details oriented, with an analytical mindsetYou are are to manage priorities autonomously and work efficiently with different stakeholdersYou are fluent in both English and French.Why Join Nalys?A people‐focused culture built on trust, development, and technical excellencePersonalized career development paths and regular follow‐up with our technical leadersAccess to a broad range of projects within the pharmaceutical and life sciences industryInternal training opportunities, communities of practice, and a strong knowledge‐sharing environment.Recruitment ProcessBy applying for this position, you will go through our standard Nalys recruitment journey:First conversation – Olivia Braszko, Talent Acquisition Specialist, will review your application and schedule an initial introduction callSecond interview – Meeting with the Business Unit Director, Jimmy Rousseaux, to validate your fit with Nalys' culture and mission. xjsrcvqHow to ApplyReady to grow your career in pharmaceutical quality?Send us your CV — we'd love to meet you!