Regulatory Affairs Manager – EU MAA’s
Training, Development, and Progression tend not to come in the same sentence when looking at new regulatory affairs vacancies – however, our client has broken the mold and they have now opened a Regulatory Affairs Manager position with the benefits of all 3 of these things. You have the option for development by working on some world class submissions (the likes of which you won't often find at some of the larger organisations) as well as learning and furthering your regulatory knowledge. Alongside this, the company has a great training scheme and offers huge potential to climb the career ladder throughout the business. Based in Essex, this international pharmaceutical company are looking for someone on a full-time basis to help with Generic submissions and marketing authorization applications for a wide array of products ready for retail. To do this, you will, therefore, have had to have full exposure to regulatory submissions and not just having worked on part of the process. You will also need:- · A degree (or equivalent) in chemistry, pharmacy or life sciences related area. · Regulatory experience including full practical experience of EU submission procedures. · Good knowledge of EU regulatory requirements for generic products. · Past CMC experience and familiarity with the content of a scientific dossier. · Some kind of line management, a supervisory or mentoring background may be desirable. For all of this, you will receive a highly competitive rate of £45,000.00 and a great benefits package including healthcare and pension plan. If you are interested in an opportunity like this, and you would like to find out more, then give me a call!