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SciPro have exclusively partnered with an innovative pharmaceutical company who are driven by their purpose to reimagine how drugs can improve the quality of life of patients with rare disease. They are a fast growing, agile organization transforming the lives of patients and care givers through the use of cutting-edge pharmaceutical technologies to translate pioneering science to medicine products.
We are supporting them on their search for a Senior Regulatory Affairs Associate to lead compliant product labelling and artwork of their product portfolio. You will join the Regulatory Affairs team in the UK and have the chance to make a real impact on multiple projects to support the company growth and ultimately, make a difference to the patients the company support.
Key Responsibilities:
Lead U.S. labelling and artwork activities
Lead the preparation of ANDA/NDA submissions
Lead promotional material submissions to the FDAKey Requirements:
4+ years of regulatory affairs experience
Experience with Adobe Illustrator or Adobe InDesign
Prior experience with US FDA regulations
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Looking for your next career move? Join a top company hiring Senior Regulatory Affairs Associate job near me in Cambridge, Cambridgeshire! This is your chance to work on exciting projects, grow professionally, and enjoy a rewarding career with competitive pay and excellent benefits. Whether you're an experienced professional or looking to take the next step, this role offers the perfect opportunity to enhance your skills and make an impact. Don’t miss out—apply today via Vita CV and take your career to the next level!
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