We are seeking a dedicated and detail-oriented Regulatory Affairs Officer EMEA to join our dynamic team. In this... Read more
We are seeking a dedicated and detail-oriented Regulatory Affairs Officer EMEA to join our dynamic team. In this role, you will be responsible for ensuring that our products comply with all regulatory requirements across the EMEA region. You will manage the submission of product registrations, keep abreast of changes in regulations, and act as the primary contact for regulatory authorities. Your expertise will be crucial in guiding our product development teams through the regulatory landscape, ensuring that all documentation is accurate and submitted in a timely manner. You will also be tasked with preparing and maintaining regulatory filings and licenses, as well as conducting gap analyses to identify areas for improvement in our processes.
The ideal candidate will possess a strong understanding of EMEA regulatory frameworks and have experience with product registration processes in the pharmaceutical, biotechnology, or medical device sectors. A degree in life sciences or a related field is required, along with a minimum of 3 years of experience in regulatory affairs. Excellent communication skills, both written and oral, are essential, as you will be liaising with cross-functional teams and external stakeholders. You should be organized, detail-oriented, and able to manage multiple projects simultaneously. If you are passionate about regulatory affairs and eager to contribute to the successful launch of innovative products, we invite you to apply for this exciting opportunity.
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