651 English-speaking jobs in Hainaut

Packaging Specialist to optimize packaging and logistics operations for automotive parts within a major international mobility player. Responsibilities include managing packaging requests, quality control, process improvement, and project management. Requires fluency in English, a Bachelor's degree in a relevant field, and experience with packaging tools and processes.

The Research Scientist – Drug Discovery Assays will develop, optimize, and execute biochemical and cell-based assays to evaluate potential therapeutic compounds. The role involves assay execution, data analysis, and collaboration with multidisciplinary teams.

The Research Scientist – Drug Discovery Assays will develop, optimize, and execute biochemical and cell-based assays to evaluate potential therapeutic compounds. The role involves assay execution, data analysis, and collaboration with multidisciplinary teams.

The Research Scientist – Drug Discovery Assays will develop, optimize, and execute biochemical and cell-based assays to evaluate potential therapeutic compounds. The role involves assay execution, data analysis, and collaboration with multidisciplinary teams.

Project Test Engineer needed for automotive sector client. Responsibilities include managing test plans, resources, and reporting progress. Requires an engineering degree and strong project management skills. Must be autonomous, analytical, and have excellent communication skills in English.

Project Test Engineer needed for automotive sector client. Responsibilities include managing test plans, resources, and reporting progress. Requires an engineering degree and strong project management skills. Must be autonomous, analytical, and have excellent communication skills in English.

Project Test Engineer needed for automotive sector client. Responsibilities include managing test plans, resources, and reporting progress. Requires an engineering degree and strong project management skills. Must be autonomous, analytical, and have excellent communication skills in English.

Packaging Specialist to optimize packaging and logistics operations for automotive parts within a major international mobility player. Responsibilities include managing packaging requests, quality control, process improvement, and project management. Requires fluency in English, a Bachelor's degree in a relevant field, and experience with packaging tools and processes.

Associate Director, AI Systems Strategist will design and deliver agentic and multi-agent AI systems across R&D, Development, and Commercial functions. Experience developing AI solutions in a Pharma, Biotech, or Med Device organization and understanding of GxP are required.

Associate Director, AI Systems Strategist will design and deliver agentic and multi-agent AI systems across R&D, Development, and Commercial functions. Experience developing AI solutions in a Pharma, Biotech, or Med Device organization and understanding of GxP are required.

Associate Director, AI Systems Strategist will design and deliver agentic and multi-agent AI systems across R&D, Development, and Commercial functions. Experience developing AI solutions in a Pharma, Biotech, or Med Device organization and understanding of GxP are required.

Lead the execution of stress testing exercises for the CIB portfolio, validate results, and analyze key drivers of risk concentrations. Present stress test outputs to various committees and risk forums, and address stakeholder inquiries. Maintain and enhance existing analysis and dashboards, and establish automated processes to analyze stress test results.

Manufacturing Tooling & Machining Process Engineer will contribute to process improvement, manage tooling activities, and investigate machining issues. Requires experience in a manufacturing environment, strong technical skills, and effective communication.

Senior Regulatory Affairs Specialist (IVD) needed for a 6-month contract. Will support product registration projects in the EMEA region, ensuring compliant market access for diagnostic products. Requires 5+ years of experience in IVD regulatory affairs and product registrations.

Senior Regulatory Affairs Specialist (IVD) needed for a 6-month contract. Will support product registration projects in the EMEA region, ensuring compliant market access for diagnostic products. Requires 5+ years of experience in IVD regulatory affairs and product registrations.

Senior Regulatory Affairs Specialist (IVD) needed for a 6-month contract. Will support product registration projects in the EMEA region, ensuring compliant market access for diagnostic products. Requires 5+ years of experience in IVD regulatory affairs and product registrations.

Experienced Device Documentation Expert needed for drug-device combination products, specializing in autoinjectors. Lead risk management, ensure regulatory compliance (ISO 13485, ISO 14971, ICH Q8/Q9/Q10/Q12, 21 CFR Part 4, EU MDR Article 117), and collaborate cross-functionally. Prepare and review device documentation (DHF, RMF, usability engineering, regulatory submissions). 8-10 years of experience in drug-device development, with expertise in medical device and combination product documentation. Fluent in English, French preferred.

Experienced Device Documentation Expert needed for drug-device combination products, specializing in autoinjectors. Lead risk management, ensure regulatory compliance (ISO 13485, ISO 14971, ICH Q8/Q9/Q10/Q12, 21 CFR Part 4, EU MDR Article 117), and collaborate cross-functionally. Prepare and review device documentation (DHF, RMF, usability engineering, regulatory submissions). 8-10 years of experience in drug-device development, with expertise in medical device and combination product documentation. Fluent in English, French preferred.

Experienced Device Documentation Expert needed for drug-device combination products, specializing in autoinjectors. Lead risk management, ensure regulatory compliance (ISO 13485, ISO 14971, ICH Q8/Q9/Q10/Q12, 21 CFR Part 4, EU MDR Article 117), and collaborate cross-functionally. Prepare and review device documentation (DHF, RMF, usability engineering, regulatory submissions). 8-10 years of experience in drug-device development, with expertise in medical device and combination product documentation. Fluent in English, French preferred.

Experienced Device Documentation Expert needed for drug-device combination products, specializing in autoinjectors. Lead risk management, ensure regulatory compliance (ISO 13485, ISO 14971, ICH Q8/Q9/Q10/Q12, 21 CFR Part 4, EU MDR Article 117), and collaborate cross-functionally. Prepare and review device documentation (DHF, RMF, usability engineering, regulatory submissions). 8-10 years of experience in drug-device development, with expertise in medical device and combination product documentation. Fluent in English, French preferred.