EMEA Regulatory Affairs Specialist – Medical Devices

International healthcare organization active in the medical device sector, supporting patient care through innovative products distributed across multiple global markets.JobomschrijvingAs a successful Regulatory Affairs Specialist - Medical Devices - EN, you will have the following responsibilities:Coordinate product registrations across assigned...

About Our ClientInternational healthcare organization active in the medical device sector, supporting patient care through innovative products distributed across multiple global markets.Job DescriptionAs a successful Regulatory Affairs Specialist - Medical Devices - EN, you will have the following responsibilities:Coordinate product registrations across...

Michael Page is seeking a Regulatory Affairs Specialist for Medical Devices (EN) to coordinate international registrations, prepare regulatory submissions, and maintain lifecycle compliance. The role involves liaising with manufacturers, distributors, and authorities, and ensuring alignment with MDR requirements.The successful candidate will have 1–3 years...

Jobat is seeking a Regulatory Affairs Specialist for an international healthcare organization active in the medical device sector. You will coordinate registrations across international markets and prepare regulatory documentation with internal and external stakeholders.You will support ongoing compliance activities, manage regulatory aspects of changes,...

At Terumo, we advance lifesaving medical technologies to benefit society. Are you eager to make a difference with us? Here, you’ll grow your expertise while staying true to your personal aspirations. Guided by our Japanese heritage, we act with respect, take ownership, and pursue continuous improvement. If you see yourself in our values, keep reading; this...

At Terumo, we advance lifesaving medical technologies to benefit society. Are you eager to make a difference with us? Here, you’ll grow your expertise while staying true to your personal aspirations.Guided by our Japanese heritage, we act with respect, take ownership, and pursue continuous improvement. If you see yourself in our values, keep reading; this...

As a successful Regulatory Affairs Specialist - Medical Devices - EN, you will have the following responsibilities: Coordinate product registrations across assigned international markets Prepare and submit regulatory documentation with internal and external stakeholders Support ongoing compliance activities for medical device portfolios Manage regulatory...

As a Regulatory Affairs Specialist, Medical Devices your responsibilities are: Coordinate medical device registrations across assigned international markets Prepare, review and submit regulatory documentation with internal and external stakeholders Support regulatory compliance and manage changes throughout the product lifecycle Review marketing materials...