Regulatory Affairs Specialist
Parets del Valles, ES
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Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. |
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<span 72="">We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.
<span 72="">We are looking for a Regulatory Affairs Specialist to join Technical department at Grifols Movaco SA.
<span 72="">The main mission will be to provide support related to the regulatory functions and management of medical devices from external suppliers that are imported and distributed by Grifols Movaco SA.
What your responsibilities will be
- <span 72="">Review the content of the processes, instructions and records that are part of the quality system related to compliance with applicable regulations and directives.
- <span 72="">Coordinate and supervise the obtaining of the documentation certifying products and their manufacturers, importers and/or distributors.
- <span 72="">Review the documentation certifying products and their manufacturers, importers and/or distributors.
- <span 72="">Prepare, review, follow up, communicate and archive the documentation generated/required for the import and/or distribution process of medical products.
- <span 72="">Carry out the necessary communications for the marketing and commissioning of medical devices.
- <span 72="">Provide the department with regulatory advice to ensure compliance with current regulations.
- <span 72="">Maintain and manage the communications made in the national registry.
Who you are
<span 72="">To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions).
- <span 72="">Bachelor's Degree in Life Sciences field is preferred.
- <span 72="">To have knowledge and experience in regulatory processes for medical devices, as well as the ability to coordinate and supervise the obtaining of the certifying documentation.
- <span 72="">2 years of experience in a similar role within pharma industry and/or medical devices.
- <span 72="">Advanced level of English.
- <span 72="">User of Microsoft Office tools, especially Excel.
- <span 72="">You are meticulous and detail oriented.
- <span 72="">You have excellent communication and teamwork skills, as well as initiative and results orientation.
<span 72="">What we offer
<span 72="">It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.
<span 72="">Information about Grifols is available at <span 72="">www.grifols.com.<span 72=""> If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply!
<span 72="">We look forward to receiving your application!
<span 72="">Grifols is an equal opportunity employer.
<span 72="">Flexibility for U Program: <span 72="">Hybrid Model
<span 72="">Flexible schedule: <span 72="">Monday-Thursday 7-10 to 16-19h and Friday 8-15h.
<span 72="">Benefits package
<span 72="">Contract of Employment:<span 72=""> Permanent position
Location: <span 72="">Parets del Vallès
Location: SPAIN : España : Parets del Valles:[[cust_building]]