3564 west flanders English-speaking jobs in Belgium

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.

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.

Business Development Manager drives new customer acquisition, cultivates existing relationships, and collaborates with technical staff and suppliers.

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.

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.

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.

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.

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.