1250 English-speaking jobs in West Flanders

Project Manager for data-centric projects, leading initiatives from internal data improvements to business transformations. Manages project scope, timelines, resources, budgets, risks, and stakeholder communication. Requires 5+ years of experience managing complex, technical projects, including data-intensive business transformations.

Project Manager for data-centric projects, leading initiatives from internal data improvements to business transformations. Manages project scope, timelines, resources, budgets, risks, and stakeholder communication. Requires 5+ years of experience managing complex, technical projects, including data-intensive business transformations.

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.

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.

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.

Orderpicker needed for day shift in a growing logistics company specializing in frozen goods. Responsibilities include picking orders, preparing them for shipment, and using an electric pallet truck. Must have experience in orderpicking or warehouse work and be comfortable working in a freezer environment.

The Product Manager B2C Sheet Vinyl owns the full residential Sheet Vinyl portfolio, managing the product lifecycle and translating consumer insights into product proposals. This role involves data-driven analysis of product performance, profitability, and customer satisfaction, as well as collaboration with R&D, operations, and marketing teams.

Project Manager for data-centric projects, leading initiatives from internal data improvements to business transformations. Manages project scope, timelines, resources, budgets, risks, and stakeholder communication. Requires 5+ years of experience managing complex, technical projects, including data-intensive business transformations.

Project Manager for data-centric projects, leading initiatives from internal data improvements to business transformations. Manages project scope, timelines, resources, budgets, risks, and stakeholder communication. Requires 5+ years of experience managing complex, technical projects, including data-intensive business transformations.

Project Manager for data-centric projects, leading initiatives from internal data improvements to business transformations. Manages project scope, timelines, resources, budgets, risks, and stakeholder communication. Requires 5+ years of experience managing complex, technical projects, including data-intensive business transformations.

Manage and optimize the international oracdecor.com website, ensuring accurate content, user experience, and SEO. Support digital marketing initiatives and collaborate with teams to align on content needs. Analyze website performance and implement improvements.