Regulatory Affairs Executive - Cambridgeshire
Are you a Regulatory professional within the pharmaceutical, clinical research or biotechnology sectors? We are looking to identify a Regulatory Affairs Executive/Regulatory Affairs Associate with a number of years experience who is looking to develop their career with a leading organisation in the Cambridgeshire area. This is a permanent role - Please contact Zest Scientific today to discuss the role in greater detailThe Regulatory Affairs Executive will provide regulatory consultancy services to a wide variety of internal and external customers, including preparation, review, submission and project management of regulatory applications. Please note: this role requires an experienced regulatory professional, and as such, we cannot accept applications from candidates without the required experience. The role: * Provide up to date regulatory advice to internal and external clients * Prepare, review, submit and project manage regulatory submissions in compliance with the applicable SOPs, regulatory guidelines and legislation * Attend client project meetings (face to face and via teleconference) * Participate in business development activities * Participate in/present at internal and external training courses and conferences The person: * Experience in regulatory affairs across CMC/biotech, clinical or pharmaceutical with experience in UK, EU and US and possibly other regions * A sound technical and scientific understanding of one or more of manufacturing, non-clinical or clinical development of pharmaceutical/healthcare products * Project experience from early stage to post marketing support * Competent IT skills including the use of MS Office applications Word, Excel, Powerpoint and Outlook * Degree or equivalent qualification in a Science subject Company and culture My client is a world renowned drug development organisation. The role of Regulatory Affairs Executive is offered on a permanent basis with a competitive salary and benefits package.