Regulatory Affairs Specialist
hace 3 semanas
Grifols, a leading global healthcare company, is seeking an experienced Regulatory Affairs Specialist to join its Biopharma Regulatory department. In this key role, you will be responsible for ensuring compliance with regulatory standards across the globe.
About the JobWe are looking for a highly skilled and detail-oriented individual to prepare, review, and manage complex submissions and follow up of product registrations or any other regulatory activity. The ideal candidate will have experience with applicable worldwide regulatory product registrations laws and regulations, as well as eCTD/CTD submissions and dossier lifecycle management.
About YouTo succeed in this role, you must have a strong background in Life Sciences, preferably with a Bachelor's degree. A minimum of 2 years of related technical and/or regulatory experience in the pharmaceutical industry is required. You should also possess advanced level English skills and be proficient in Microsoft Office tools.
About GrifolsAs a global leader in plasma-derived medicines and transfusion medicine, Grifols is committed to improving the health and well-being of people around the world. We believe in fostering an inclusive environment that values diversity and promotes equal employment opportunities.
What We OfferIn return for your expertise, we offer a competitive salary range of $80,000 - $110,000 per year, depending on your level of experience. Additionally, you will enjoy a flexible schedule, Monday-Thursday 7-10 to 16-19h and Friday 8-15h, and a comprehensive benefits package. If you are passionate about regulatory affairs and want to make a meaningful contribution to our team, please apply for this exciting opportunity.
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