Regulatory Affairs Specialist - Benelux (MA & MDR)

airliquidehr; Zaventem; Sur place; EUR 45 000 - 60 000; Plein temps

Résumé du poste

Air Liquide Medical Ltd. NV is seeking a Regulatory Affairs Specialist in Zaventem. Your role includes managing submissions of Marketing Authorization Applications and ensuring compliance with medical device regulations. You'll monitor progress with authorities and communicate decisions effectively.

The ideal candidate has 3-5 years of experience in a pharmaceutical environment, is a good communicator, and is fluent in French, Dutch, and English. Join us in our mission to support healthcare professionals and patients effectively.

Qualifications

• 3-5 years professional experience in regulatory affairs in a pharmaceutical environment.
• Ability to work under stress and remain steadfast in challenging situations.
• Strong accuracy and organizational skills.

Responsabilités

• Submit new Marketing Authorization Applications (MA’s) to the relevant authorities.
• Collaborate with corporate for European procedures on MA’s.
• Monitor progress and communicate decisions to stakeholders.

Connaissances

Pharmaceutical regulatory experience

Team player

Good communication skills

Analytical skills

Multi-language (French, Dutch, English)

Description du poste

Air Liquide Medical Ltd. NV is seeking a Regulatory Affairs Specialist in Zaventem. Your role includes managing submissions of Marketing Authorization Applications and ensuring compliance with medical device regulations. You'll monitor progress with authorities and communicate decisions effectively.

The ideal candidate has 3-5 years of experience in a pharmaceutical environment, is a good communicator, and is fluent in French, Dutch, and English. Join us in our mission to support healthcare professionals and patients effectively.