A leading life sciences organization in Spain is seeking an experienced Regulatory Affairs Specialist to manage regulatory impact assessments, annual registrations, and global submissions, particularly to the FDA.
Todos los candidatos deben asegurarse de leer atentamente la siguiente descripción del puesto y la información antes de enviar su solicitud.
The ideal candidate will have a Bachelor's degree and a minimum of 4 years of experience in Regulatory Affairs within the medical device sector.
Strong communication and problem-solving skills are essential, and fluency in English is required. xhfqzwm
This position offers a unique opportunity to collaborate with global partners and contribute to compliance and timely submissions.
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