637 English-speaking jobs in Hainaut

Risk Model Strategy Expert provides authoritative challenge and advice on credit risk models, drives model monitoring evolution, and translates complex risk dynamics into actionable insights for senior management.

The Engineering Manager will lead the local engineering team and be responsible for all engineering activities related to automation systems within the European Distribution Center (EDC) and the broader EMEA region. This role will support the development and implementation of automation system plans for both brownfield and greenfield projects, as well as equipment upgrades. The incumbent will lead projects through operational stabilization, providing technical guidance to the local team. The manager will also ensure compliance with regulations and budget consistency, while also developing standard operating procedures.

The Team Within IRO, the Model Strategy & Monitoring team steers the regulatory model strategy, ensures that group-wide modelling and monitoring methodologies, model life cycle governance and frameworks remain robust and forward-looking, and oversees & controls model use across ING's global organisation.

Experienced SAP FS-PM Design & Development Lead needed for a 6-month remote contract. Responsibilities include designing, configuring, and implementing SAP FS-PM solutions, leading development teams, and supporting testing and deployments. Requires 6+ years of SAP FS-PM experience, ABAP/ABAP OO development skills, and expertise in Policy Management. Strong understanding of insurance business processes is essential.

Experienced SAP FS-PM Design & Development Lead needed for a 6-month remote contract. Responsibilities include designing, configuring, and implementing SAP FS-PM solutions, leading development teams, and supporting testing and deployments. Requires 6+ years of SAP FS-PM experience, ABAP/ABAP OO development skills, and expertise in Policy Management. Strong understanding of insurance business processes is essential.

Experienced SAP FS-PM Design & Development Lead needed for a 6-month remote contract. Responsibilities include designing, configuring, and implementing SAP FS-PM solutions, leading development teams, and supporting testing and deployments. Requires 6+ years of SAP FS-PM experience, ABAP/ABAP OO development skills, and expertise in Policy Management. Strong understanding of insurance business processes is essential.

As a Visual Inspection Specialist, you will act as the subject matter expert for automated visual inspection technologies in a pharmaceutical manufacturing environment. You will define user requirements, support supplier selection, and ensure compliance with GMP regulations.

As a Visual Inspection Specialist, you will act as the subject matter expert for automated visual inspection technologies in a pharmaceutical manufacturing environment. You will define user requirements, support supplier selection, and ensure compliance with GMP regulations.

Lead the direction of AI across products and organization. Shape AI features, mature data foundations, experiment with AI applications, and make strategic AI decisions.

Lead the direction of AI across products and organization. Shape AI features, mature data foundations, experiment with AI applications, and make strategic AI decisions.

Lead the direction of AI across products and organization. Shape AI features, mature data foundations, experiment with AI applications, and make strategic AI decisions.

Expert Consultant to support a pharmaceutical company's strategic project. Focus on documentation activities for automated systems and manufacturing equipment, including IQ, OQ, and PQ protocols. Requires DeltaV or VSI expertise, GMP/GxP knowledge, and strong documentation skills.

Expert Consultant to support a pharmaceutical company's strategic project. Focus on documentation activities for automated systems and manufacturing equipment, including IQ, OQ, and PQ protocols. Requires DeltaV or VSI expertise, GMP/GxP knowledge, and strong documentation skills.

Expert Consultant to support a pharmaceutical company's strategic project. Focus on documentation activities for automated systems and manufacturing equipment, including IQ, OQ, and PQ protocols. Requires DeltaV or VSI expertise, GMP/GxP knowledge, and strong documentation skills.

As a Visual Inspection Specialist, you will act as the subject matter expert for automated visual inspection technologies in a pharmaceutical manufacturing environment. You will define user requirements, support supplier selection, and ensure compliance with GMP regulations.

Senior Asset Manager providing portfolio, program, and project support. Ensures effective delivery of support services across projects. Requires NATO SECRET clearance and 7 years of relevant experience.

Leads inspection management and readiness activities for a global Pharmacovigilance organization. Supports regulatory inspections and collaborates with cross-functional teams to ensure compliance with GVP, GCP, and GLP. Requires 5-8 years of experience in Pharmacovigilance, GVP Quality, Quality Assurance, or Auditing with proven experience in inspection management.

Leads inspection management and readiness activities for a global Pharmacovigilance organization. Supports regulatory inspections and collaborates with cross-functional teams to ensure compliance with GVP, GCP, and GLP. Requires 5-8 years of experience in Pharmacovigilance, GVP Quality, Quality Assurance, or Auditing with proven experience in inspection management.

Leads inspection management and readiness activities for a global Pharmacovigilance organization. Supports regulatory inspections and collaborates with cross-functional teams to ensure compliance with GVP, GCP, and GLP. Requires 5-8 years of experience in Pharmacovigilance, GVP Quality, Quality Assurance, or Auditing with proven experience in inspection management.

Experienced QA Officer needed for a fixed-term contract in Eastern Belgium. Provide quality assurance support across GMP manufacturing operations, review documentation, lead investigations, and ensure compliance with GMP and regulatory standards. Experience with validation activities, including CSV, is required.