Medical Devices Regulatory Expert - Specialist Pharma
- Experience Level
Medical Devices Regulatory Expert for a Specialist Pharma Company in North West London/Middlesex. This is an excellent role for a Regulatory Affairs professional within Medical Devices. This role would suit a Regulatory Manager, Project Manager or top-end Principal/Senior Regulatory Associate with several years’ experience ready to take a 'step-up'.
Working for a mid-sized Specialist Pharma Company, you will be concentrating on Class I, II and III Medical Device products – In-vitro Diagnostics and Active Implantable Medical Devices.
CE Marking and good working knowledge of the European Medical Device Directive. On-going Life-cycle maintenance activity. Subject Matter Expertise in Medical Devices. Formulation of robust strategies for implementation regarding any changes to documentation.
The role requires an individual who is adept in multi-tasking, and has excellent influencing and negotiating skills. In addition, you will possess the ability to analyse and interpret complex issues and develop effective strategies.
An excellent salary package awaits the successful candidate. Based in North West London/Middlesex.
If you are interested in this, or any other Regulatory Affairs roles, please get in touch with Julian Turner at Turner Regulatory Recruitment on 0203 695 9477/07447 977 330 or by clicking Apply Now.
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