Regulatory Affairs Documentation Specialist

hace 3 semanas

Valencia, España Grifols, S.A A tiempo completo

Regulatory Affairs Documentation Specialist 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.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.We are looking for a Regulatory Affairs Documentation Specialist to join Biopharma Regulatory department.What your responsibilities will bePrepare, review, follow up, communicate, and archive documentation generated at the Regulatory Affairs department or needed for a regulatory submission.Request from other Grifols departments, affiliates or outside companies anything that is required for a regulatory submission.Maintain regulatory record filing systems for Regulatory Affairs in both hard copy and electronic filing formats, process incoming and outgoing correspondence.Assist Regulatory Affairs department to meet business objectives.Who you areTo 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.Bachelor's Degree in Life Sciences field is preferred.Minimum 6 months of related technical and/or regulatory experience in pharmaceutical industry or an equivalent combination of education and experience.Advanced level of English.User of Microsoft Office tools.You are meticulous and detail-oriented.You have excellent communication and teamwork skills, as well as initiative and results orientation.What we offerIt 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.Information about Grifols is available at www.Grifols.Com. If you are interested in joining our company and you have what it takes for such an exciting position, then don't hesitate to applyWe look forward to receiving your applicationGrifols is an equal opportunity employer.Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h.Benefits packageContract of Employment: Permanent positionFlexibility for U Program: Occasionally remote#J-18808-Ljbffr

  • Regulatory Affairs Documentation Specialist

    hace 3 semanas

    Valencia, España Grifols Sa A tiempo completo

    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...

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    hace 2 semanas

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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...

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