Regulatory Affairs Officer
Regulatory Affairs Officer East Anglia 12 Month Contract Offering up to 40p/h DOE A leading pharmaceutical organisation are actively looking for a Regulatory Affairs Officer to join their established team due to a project back fill. Within this position you will be responsible for creation, review and approval of cGMP submissions. The successful candidate will be principally responsible for one product and also provide any required assistance necessary within the team. Job Responsibilities include; - Manage and maintain regulatory quality systems and documentation - Evaluate effects of new changes to legislation on current operations and provide solutions - Act as a source of technical expertise - Document legislation - Managing regulatory dossiers Candidate Requirements include; - Life Sciences degree or equivalent - Regulatory CMC experience is desirable - Prior experience with GMP for either office or manufacturing sites - Experience with change control system - Prior experience using documentum would be highly advantageous If this position is of interest to yourself please give Sophie at Regulatory Professionals a call on 0118 952 2797 or alternatively forward your up to date CV to firstname.lastname@example.org.