Regulatory Affairs Officer
Are you experienced in Regulatory Affairs in the Medical Device industry and looking for your next contract role? This could be your opportunity to work at one of the world's leading Biopharmaceutical companies, a chance to gain some fantastic experience and enhance your CV.
The role - For this six-month contract you will be using your knowledge of European Regulatory Affairs, specifically in the Medical Device sector, along with experience of dealing with ISO 13485 on a daily basis. The main focus for this position will be to compile and maintain technical documentation to meet the Medical Devices Directive as well as managing updates of existing product registrations in EMEA.
Skills - It goes without saying that you will have to have a Regulatory Affairs background, specifically in the medical device field would put you top of the list! Your ability to communicate effectively is key due to the nature of the role liaising globally with cross functional teams.
The company - This globally recognised manufacturer with sites throughout the world who work across a range of sectors including Biopharmaceuticals, Medical, Aerospace, Power and Utilities. This specific site is based just outside of Portsmouth and offers a modern and friendly office along with free parking, subsidised canteen on site and stunning views over the Solent.
The package - This position is expected to last for six months. The standard working hours are 09:00am to 17:15pm Monday to Thursday and 09:00am to 16:15pm on Friday. The payrate will be supplied upon application.
If this role sounds exactly what you are looking for the either Click the Apply button now or call Sam Pratley at our Havant office on 02392 453377 to discuss the role further.
*All limited company contractors will be working inside IR35
Note: this is the location of the town or city the job is in and not the exact location of the employer.