3811 west flanders English-speaking jobs in Belgium

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.

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.

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.