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hace 1 semana
Grifols, a global healthcare company, is seeking a highly skilled Regulatory Affairs Specialist to join its Technical department at Grifols Movaco SA in Parets del Vallès, Spain. With over 110 years of experience in improving the health and well-being of people around the world, Grifols is committed to equal employment opportunities that foster an inclusive environment.
About the RoleThe successful candidate will be responsible for providing support related to regulatory functions and management of medical devices from external suppliers imported and distributed by Grifols Movaco SA. Key responsibilities include reviewing content related to compliance with applicable regulations and directives, coordinating the obtaining of documentation certifying products and their manufacturers, importers, and distributors, and preparing and reviewing documentation generated or required for the import and/or distribution process of medical products.
RequirementsTo perform this job successfully, candidates must have a Bachelor's Degree in Life Sciences field, knowledge and experience in regulatory processes for medical devices, and the ability to coordinate and supervise the obtaining of certifying documentation. Additionally, advanced level of English, user of Microsoft Office tools, especially Excel, meticulous and detail-oriented skills, excellent communication and teamwork skills, as well as initiative and results orientation are essential.
What We OfferGrifols offers a competitive salary of approximately €45,000 - €60,000 per year, depending on experience, plus a benefits package including flexibility for U Program: Hybrid Model Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h, contract of employment: Permanent position, and location: Parets del Vallès, Spain. If you are interested in this exciting opportunity, please don't hesitate to apply.