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Regulatory Affairs Specialist - Medical Devices - Bedfordshire
A fantastic opportunity has arisen for a Regulatory Affairs Specialist to join a UK based Medical Devices organisation. This worldwide Medical Devices Company provides unique health and environmental services locally and globally has over 20,000 members and 1000 offices worldwide. They specialise in delivering High Regulatory and Quality standards along with conducting a high reputation for helping customers increase the value of their life saving products.
As the Regulatory Affairs Specialist you will report directly to the Regulatory Affairs Manager and you will have the following responsibilities:
Clearly demonstrate good working knowledge of ISO 13485 and ISO Medical Device Directive, experience in meeting regulatory requirements (CE Marking, FDA). You will be providing strong regulatory support within the offices being the main point of contact to see to issues raised by the worldwide offices along with client issues and certification. Furthermore, you will possess excellent communication and interpersonal skills have good leadership skills. This experience will preferably have been gained in the Medical Device sector.
Additionally you should experience in a regulated environment. You should be organised, interpersonal, focused, computer literate, motivated, confident, mature and professional with excellent written/verbal communication skills, presentation skills, and interpersonal skills.
Subsequently they are looking for someone to come in and be a good communicator and a great influencer to the business proving solutions along with strengthening a team.
This is an exceptional opportunity within a flexible organisation who offers rewarding careers. If you want to be a part of this exciting opportunity who offers a competitive salary, excellent benefits package, including company pension, Life Assurance, and Healthcare, please contact Ekta Multani, Recruitment Consultant at Paramount Recruitment 0121 616 3474.
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