Regulatory Affairs Associate
Description : 24 Mar, 2023
Keen to step into a role that offers true autonomy and make your mark within the Regulatory Affairs space? I-Pharm has partnered with a dynamic and rapidly expanding global Pharmaceutical. This innovator is in an exponential phase of growth and are looking to add to their global team. This expansion is due to an ever expanding project pipeline and increased investment in state of the art technologies. As a result, they are looking to hire a Regulatory Affairs Associate on a permanent basis to join the business during this exciting time. The role would allow you to develop and progress your career in a supportive, growth positive environment. The role will involve but not be limited: Support product information repositories. Support and the management of systems and processes. Be responsible for, the maintenance and QC of product information. Support and be responsible for certain projects. Input into training and professional development activities in order to fulfil departmental objectives. Responsible for, the training of others and mentoring. Understanding of internal customers. Optimisation processes of internal customers. Understand best practise and make recommendations. As a Regulatory Affairs Associate, you will need: 1 - 3 years of experience within regulatory affairs in either the medical device or in vitro diagnostics. Regulatory knowledge and understanding of requirements and processes in the EU. Artwork generation / review experience Experience with the preparation/ review of technical files I am a market expert in the Regulatory Affairs area working with a large variety of clients across the pharmaceutical, biotechnology, and medical device industries. If this role is of interest to you, or if you'd like to explore other opportunities in the market, please feel free to contact me directly. Contact Sandeep Bains - /
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