Offres de Deviations à Lee

*Packaging Deviation & Continuous Improvement Specialist** 📍 Brussels Area, Belgium *Introduction** At *Nalys** , we empower talented professionals to grow their careers within leading life sciences environments. We are currently looking for a *Packaging Deviation & Continuous Improvement S

Validation Engineer – Lab Equipment In this role, you support the validation and implementation of laboratory equipment within a regulated pharmaceutical environment. You ensure equipment is properly validated, compliant with GMP requirements, and ready for operational use in analytical and microbio

Dans le cadre du démarrage d’une nouvelle zone de production pour l’un de nos clients du secteur pharmaceutique, nous recherchons un(e) QA CSV pour renforcer l’équipe CSV. Vous serez en charge d'assurer la conformité des activités de qualification des systèmes informatisés (CSV) aux exigences réglem

Job Description Deviation Management Specialist Key Responsibilities Lead the end-to-end management of deviations, including investigation, root cause analysis (RCA), impact assessment, and corrective and preventive actions (CAPA). Ensure all deviations are documented, tracked, and resolved in compl

*Job Description** *Deviation Management Specialist** *Key Responsibilities** Lead the end-to-end management of deviations, including investigation, root cause analysis (RCA), impact assessment, and corrective and preventive actions (CAPA). Ensure all deviations are documented, tracked, and resolved

🔍 Responsible Person 📍 Location: Hybrid 🕓 Type: Full-time We are looking for colleagues who are interested in taking up the role of Responsible Person (RP) for GDP-related activities within client projects. This is an internal opportunity for consultants who meet the legal requirements to act as

Nalys

Compliance Support – Pharmaceutical Industry 📍Walloon Brabant, Belgium Introduction At Nalys, we partner with leading pharmaceutical organizations to support their most critical operations. We are currently looking for a Compliance Support Consultant to reinforce one of our partners’ manufacturing

Amaris Consulting

Job Description Are you experienced in equipment, system and process qualification/validation within the pharmaceutical industry? Do you want to play a crucial role in ensuring compliance, quality and reliability across the full lifecycle of facilities and systems? Then this role is an excellent mat

Amaris Consulting

Job Description Are you a Cleaning Validation expert looking for a key role in a high-tech pharmaceutical manufacturing environment? Do you want to contribute to safe, compliant processes while supporting the introduction of new products and equipment? Then this opportunity is made for you! As a Cle

Arcadis

Ben jij een kwaliteitsgedreven professional met ervaring in equipment qualification binnen een cGMP-omgeving? Werk je graag in een technisch complexe en sterk gereguleerde omgeving waar kwaliteit en compliance centraal staan? Dan is deze uitdaging iets voor jou. Als QA Qualification ben je verantwoo

Abylsen

Ervaring: 3–5 jaar relevante QA-ervaring Sector: Life Sciences / Farma / Biotech Ben jij kwaliteitsgericht, analytisch sterk en klaar voor een rol waarin je zowel intern als extern het verschil maakt? Voor onze klant in de farmaceutische sector zoeken wij een QA Release & Alliance Engineer die funge

Amaris Consulting Belgium SPRL

*Job Description** *Mission Overview** Lead the governance and performance optimization of the *Deviation Management Process,** driving sustainable quality improvements across pharmaceutical operations. This role combines strategic oversight with hands-on process leadership to reduce quality inciden

SABCA

At our Lummen site, SABCA Limburg, we are specialized in the manufacturing of high-tech composite assemblies for aircraft. On the one hand, we produce integrated skins for flaps and stabilizers using two automatic tape-layers and very large autoclaves and of course, our colleagues’ extended know-how

Site Name: Belgium-Wavre Posted Date: Feb 24 2026 Position Summary You will manage a QC laboratory team at our Belgium site, leading daily laboratory operations and coaching people. You will ensure high-quality results, regulatory compliance, and a safe working environment. You will partner with QA,

Position Summary You will manage a QC laboratory team at our Belgium site, leading daily laboratory operations and coaching people. You will ensure high-quality results, regulatory compliance, and a safe working environment. You will partner with QA, manufacturing, logistics and support functions to

Vulcain Engineering Group | Belgium

44 000 € - 59 000 € /an

Vulcain Engineering Belgium is looking for a Deviation Specialist to join its team. As a Deviation Specialist at Vulcain Engineering Belgium, you will work on projects in the biotech or pharmaceutical industries, from process design to commissioning, and be involved in all phases of a project accord

Arcadis

Are you analytically strong, quality-driven, and passionate about method validation within a GMP environment? Then this opportunity might be for you. As a Lab Operations Project Engineer, you are responsible for the compliance assessment of method validation and compendial compliance dossiers. You p

Vulcain Engineering Group | Belgium

44 000 € - 55 000 € /an

Vulcain Engineering Belgium is looking for a QA Engineer to join its consulting team. ABOUT THE POSITION: Ensure all aspects of product manufacturing and/or testing are reviewed versus established quality standards and the applicable marketing authorizations. Manage quality systems, e.g. change cont

Vulcain Engineering Group | Belgium

*Vulcain Engineering Belgium** is looking for a *Deviation Specialist to join its team.** As a *Deviation Specialist** at Vulcain Engineering Belgium, you will work on projects in the biotech or pharmaceutical industries, from process design to commissioning, and be involved in *all phases of a proj

Vulcain Engineering Group | Belgium

44 000 € - 59 000 € /an

Vulcain Engineering Belgium is looking for a QC Technician to join its team. ABOUT THE POSITION: Operational Perform QC analytical testing on biopharmaceutical products (Drug Substance, Drug Product, Finished Goods), including HPLC, UV, ELISA, electrophoresis, bioassays, DNA threshold, IPC, release,