This job is no longer available
Senior Regulatory Affairs Manager - South East
£50,000 - £60,000
An excellent opportunity has arisen for a Regulatory Affairs Manager to come a join a global Medical devices organisation that has a strong presence worldwide. This fantastic organisation provides all round solutions for Medical Devices, Medical Technologies and Pharmaceutical. They have expert teams that provide all rounded devices to help improve patient care worldwide. This is an excellent opportunity for a Regulatory Affairs professional looking for a new challenging career.
The purpose of the role is to provide Regulatory Affairs support and work closely with other Regulatory Affairs groups in Medical Diagnostics. You will be responsible for lead cross financial activities for the Regulatory decisions for the UK/USA. You will be closing collaborating with other Regulatory groups centrally and nationally liaising with regional heads of the company. You will also be keeping track of regulatory advice and new developments.
You will be working closely with external regulatory bodies as and when required to provide appropriate input into regulatory plans and strategies. To identify and provide advice and guidance on worldwide regulations throughout the organization and to ensure that up to date knowledge is maintained and implemented within the company. You must have have a depth of understanding of healthcare environment and ability to work independently showing the ability to demonstrate initiative and attention to detail, good problem solving skills is vital and the ability to work to deadlines across multiple simultaneous projects.
The working environment and quality of work within the business are of the highest order and the successful individual can expect to be well rewarded both with their career development. Subsequently they are looking for someone to come in and be a good communicator and a great influencer to the business proving solution. This is a new role that is growing rapidly; this position would potentially suit a candidate looking for a new challenge along with demonstrating their abilities.
If successful, you will be rewarded with a completive salary and an excellent benefits package. If you want to be a part of this exciting, challenging opportunity, please contact Ekta Multani, Quality Assurance and Regulatory Affairs Recruitment Consultant within the Medical Devices Division at Paramount Recruitment, on 0121 616 3474.
Regulatory Affairs Associate jobs, Compliance jobs, Quality Assurance jobs, Regulatory Affairs jobs, Medical Devices jobs, ISO 13485 jobs, FDA jobs, 21 CFR Part 820 jobs, QMS jobs, FDA 510k jobs, ISO 13485 jobs, Regulatory Affairs jobs, Regulatory Affairs Specialist jobs, MDD jobs, CE Marking jobs, MDD jobs, Medical Device Directive Jobs, Medical Imaging Jobs, Electro-Mechanical Jobs, Electro-Mechanical Medical Devices Jobs, EN 60601 Jobs, RA Jobs, QA Jobs
Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.