3564 west flanders English-speaking jobs in Belgium

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.

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.

Regional Sales Manager for Geely's Belgium & Luxembourg market. Drive dealer network success by defining sales targets, managing performance, and optimizing sales funnels. Analyze market trends, collaborate with internal teams, and ensure a premium customer experience. Requires 3-5 years of field-based sales or network management experience in the automotive industry, strong Funnel Management skills, and fluency in Dutch, French, and English.

Regional Sales Manager for Geely's Belgium & Luxembourg market. Drive dealer network success by defining sales targets, managing performance, and optimizing sales funnels. Analyze market trends, collaborate with internal teams, and ensure a premium customer experience. Requires 3-5 years of field-based sales or network management experience in the automotive industry, strong Funnel Management skills, and fluency in Dutch, French, and English.

Regional Sales Manager for Geely's Belgium & Luxembourg market. Drive dealer network success by defining sales targets, managing performance, and optimizing sales funnels. Analyze market trends, collaborate with internal teams, and ensure a premium customer experience. Requires 3-5 years of field-based sales or network management experience in the automotive industry, strong Funnel Management skills, and fluency in Dutch, French, and English.

Regional Sales Manager for Geely's Belgium & Luxembourg market. Drive dealer network success by defining sales targets, managing performance, and optimizing sales funnels. Analyze market trends, collaborate with internal teams, and ensure a premium customer experience. Requires 3-5 years of field-based sales or network management experience in the automotive industry, strong Funnel Management skills, and fluency in Dutch, French, and English.

Regional Sales Manager for Geely's Belgium & Luxembourg market. Drive dealer network success by defining sales targets, managing performance, and optimizing sales funnels. Analyze market trends, collaborate with internal teams, and ensure a premium customer experience. Requires 3-5 years of field-based sales or network management experience in the automotive industry, strong Funnel Management skills, and fluency in Dutch, French, and English.

Regional Sales Manager for Geely's Belgium & Luxembourg market. Drive dealer network success by defining sales targets, managing performance, and optimizing sales funnels. Analyze market trends, collaborate with internal teams, and ensure a premium customer experience. Requires 3-5 years of field-based sales or network management experience in the automotive industry, strong Funnel Management skills, and fluency in Dutch, French, and English.

Regional Sales Manager for Geely's Belgium & Luxembourg market. Drive dealer network success by defining sales targets, managing performance, and optimizing sales funnels. Analyze market trends, collaborate with internal teams, and ensure a premium customer experience. Requires 3-5 years of field-based sales or network management experience in the automotive industry, strong Funnel Management skills, and fluency in Dutch, French, and English.

Regional Sales Manager for Geely's Belgium & Luxembourg market. Drive dealer network success by defining sales targets, managing performance, and optimizing sales funnels. Analyze market trends, collaborate with internal teams, and ensure a premium customer experience. Requires 3-5 years of field-based sales or network management experience in the automotive industry, strong Funnel Management skills, and fluency in Dutch, French, and English.