Senior International Regulatory Affairs Specialist - South East
An excellent opportunity has arisen for a Senior International Regulatory Affairs Specialist to come a join a respected 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 knowledge and work closely with other Regulatory Affairs groups to prepare high quality documentation for regulatory submissions. Along with providing regulatory advice on certain projects that are assigned. You will be responsible for liaising with other relevant departments to make sure that regulatory requirements are met accurately and approvals are made, communicating accordingly. You will be effectively planning submissions and documents to agreed timeline. Provide regulatory advice, identify and resolve regulatory issues within the departments or country offices that a relevant.
You will have a decision making responsibly within the role. You will be responsible to interact with all function of the organisation when necessary. You will be responsible for interacting with major regulatory authorities with minimal supervision. You must have relevant experience within the Medical Devices or Pharmaceutical industry within Regulatory Affairs. You must also have hands on experience Of Quality Management systems QMS and Six Sigma
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.
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 or ekta.multani@paramountrecruitment.co.uk.
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