Company: Regulatory Professionals
Closing Date: 12 May 17
Salary (£): On Application
Regulatory Affairs Specialist (Medical Devices) Duration: 12 Month contract: Leeds Regulatory Professionals are currently working with a leading pharmaceutical company and are looking for a Regulatory Affairs Specialist on a contract basis.
Regulatory Affairs Specialist (Medical Devices)
Duration: 12 Month contract
Regulatory Professionals are currently working with a leading pharmaceutical company and are looking for a Regulatory Affairs Specialist on a contract basis. The role with give you the opportunity to assist with the preparation of global submissions of classes II and III.
Your Duties will include:
*Leading the submission of licences and authorisations.
*Provide regulatory guidance to the product development teams in strategic planning and pre-marketing
*Involvement of the planning for regulatory deliverables on given projects
*Maintenance of existing products, international registrations and dossiers
*Approve labelling, packaging, advertising and promotional materials
*Relevant Bachelors Degree
*Hands on experience with the preparation and submission for Class II and III
*Experience submitting to EU and US
*Experience of International regulations in China, Japan, Brazil and Russia is desirable
*Strategic regulatory knowledge
*Ability to influence key stakeholders
*Excellent written, verbal and presentation skills
If you are looking for you next contract positions and available for a 12 month contract then please get in touch ASAP, this is a great opportunity to work for a global pharmaceutical company.
Not for you, but know someone who is looking? We offer a referral scheme whereby, for any candidate referred to us (who secures a job) we will give you £250 in vouchers*. *terms and conditions apply
Keywords: Regulatory, Regulatory Affairs Specialist, Medical Device, Class II and III, Submissions, EU, US, Leeds, Contract
3rd floor 33 Blagrave Street Reading
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