Our client is a high-growth, Manchester-based pharmaceutical company operating in a highly-specialist field. The business is entering a rapid period of growth after gaining EMA (European Medicines Agency) approval on their first product, with a strong pipeline of additional products undergoing various stages of product authorisation and approval.
With further growth and product development projects, now is the ideal time to join their regulatory affairs team.
In this role you will be providing regulatory support for all activities within the company, including IMPD compilation, variations, change impact assessments, periodic safety update reports amongst other tasks and duties. Your role very much sits at the fulcrum of new product development and commercialisation, and you will be working in a highly-experienced team that has ‘been there and done it’.
You will have a life science, pharmacy or chemistry degree and subsequently will have gone on to gain regulatory exposure in the pharmaceutical environment. You will have enjoyed exposure to regulatory agencies and have a ‘growth mindset’ ie; willing to work in areas that you have not done previously to help the company grow further in the future. Any experience of designing new ways of working to drive efficiency would be well received and highly beneficial.
Role: Regulatory Affairs Specialist / Manager
Salary: Very flexible + benefits
For more information or to apply for this position, please contact our consultant Chris Bate, quoting the reference GH/12433/w sending your CV including full career details, notice period and your current salary via email to: email@example.com or telephone 01928 711800 for an initial discussion.
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