An opportunity arisen to work for a well establish company in the NW area. This position involves supporting the development of a pipeline of generic pharmaceuticals Responsibilities Liaise with the QA department and the manufacturing and development sites to get the required data to populate the dossier Provide strategic regulatory advice on development projectsPrepare scientific advice requests and attend meetings with MHRA and other national competent authorities Write Module 1 and Module 3, Prepare Module 2, Prepare MAA (dossier) Liaise with clinical consultants to prepare the non-CMC parts of the dossier Prepare associated regulatory submissionsManage regulatory procedures at both EU and UK national level from application through to approval Qualification and experience Successful candidate will have minimum BSc in Life Sciences, Chemistry or related discipline with 4 years’ experience in Regulatory affairsGood Knowledge of Clinical development activities would be desirable Experience with generic drug development programmesPre and post marketing experienceStrong communication skills (both written and orally) Attention to detail Efficient and timeline/target orientated Ability to work both independently and within a team To apply for this position, candidates must be living in the UK eligible to work