Automation Engineer Pharmaceuticals F/M/X - Courcelles

We are seeking a highly motivated Automation Engineer to serve as the onsite specialist for a state-of-the-art European Distribution Centre hub supporting one of the world's leading healthcare organizations. · ...

We are seeking a highly motivated Automation Engineer to serve as the onsite specialist for a state-of-the-art European Distribution Centre hub. · A key responsibility includes leading planned maintenance system upgrades during weekend windows to ensure zero impact on daily opera ...

We are offering international volunteer positions VIE for talented engineers and compliance specialists to support critical operations across our pharmaceutical sites in Belgium. · These roles are ideal for early-career professionals seeking hands-on experience in a regulated ind ...

The candidate will lead the IT integration project for pharmaceuticals with SAP S/4HANA implementation. The goal is smooth transition with zero disruption to GMP operations. · Map current business processes against SAP S/4HANA capabilities · Facilitate ERP workshops document gaps ...

Job Description · Key Responsibilities · Validation Strategy & Documentation · Ensure a comprehensive and compliant validation lifecycle, including: · Development, review, and approval of validation documentation: · Validation Plan (VP) · IOQ/PQ validation protocols (equipment ...

Lead the IT integration project for Pharmaceuticals company in Brussels. · Bachelor's or Master's in Computer Science, Automation Engineering, or related field. · 7–10 years of hands-on experience in operational IT within manufacturing environments. · ...

We are offering international volunteer positions (VIE) for talented engineers to support critical operations across our pharmaceutical sites in Belgium. · You will work within cross-functional teams on projects related to facility qualification process optimization regulatory co ...

Lead the IT integration project, ensuring a smooth transition to SAP S/4HANA with zero disruption to GMP operations. · ...

Job Description · Key Responsibilities · Validation Strategy & Documentation · Ensure a comprehensive and compliant validation lifecycle, including: · Development, review, and approval of validation documentation: · Validation Plan (VP) · IOQ/PQ validation protocols (equipment an ...

We are offering international volunteer positions (VIE) for talented engineers to support critical operations across our pharmaceutical sites in Belgium. · CQV / Process Engineer (Commissioning, Qualification & Validation) · Manufacturing Support / GMP Compliance Engineer · EHS E ...

The candidate will lead and execute the end-to-end validation process for the Siemens Opcenter upgrade: develop test protocols, perform protocol reviews, execute test cases, document findings, prepare final validation summary report. · Bachelor's degree in Engineering (Electrical ...

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 ...

We are looking for an EHS Engineer with an experience in pharmaceuticals. · Key Responsibilities · Risk Analysis & Field Work · – Conduct on-site inspections of warehouse zones, chemical-storage rooms and ADR areas.Draft and update activity sheets · Safety data sheets · ...

Job Description · Mission Overview · Lead utilities harmonization for integration, ensuring seamless transition while maintaining zero supply risk. Bridge legacy sytems to standards through rigorous GMP compliance and cross-functional coordination. · Technical Takeover & Assessm ...

We are looking for an EHS Engineer with an experience in pharmaceuticals.You will own the end-to-end delivery of circa 30 risk analyses for warehouse and chemical-storage areas, ensuring full ADR, ergonomics and chemical-storage compliance across the site. · ...

We are an independent technology consulting firm providing guidance and solutions to businesses. · Amaris Consulting is proud to be an equal opportunity workplace. · ...

++Join a high-performing EHS team in a pharmaceutical production site.+ · +You will embed the EHS management system,+roll out the "dangerous situation" reporting tool to all managers,+and ensure CP2 compliance.<+This is a hands-on, shop-floor role requiring proven pharma manufact ...

We are currently looking for several professionals to join our R&D team for a large-scale process and analytical development project based in Brussels. · This project involves protein-based biochemistry and chromatography, supporting innovation in life sciences.You will be part o ...

Job Description · MES project: · System upgrade · Limited reprogramming (scope defined, focused on critical changes) · Full validation lifecycle (including test protocol development, execution, reporting, and post-upgrade monitoring) · No formal training provided on the new versi ...

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 red ...