Naukrijobs UK
Register
London Jobs
Manchester Jobs
Liverpool Jobs
Nottingham Jobs
Birmingham Jobs
Cambridge Jobs
Glasgow Jobs
Bristol Jobs
Wales Jobs
Oil & Gas Jobs
Banking Jobs
Construction Jobs
Top Management Jobs
IT - Software Jobs
Medical Healthcare Jobs
Purchase / Logistics Jobs
Sales
Ajax Jobs
Designing Jobs
ASP .NET Jobs
Java Jobs
MySQL Jobs
Sap hr Jobs
Software Testing Jobs
Html Jobs
IT Jobs
Logistics Jobs
Customer Service Jobs
Airport Jobs
Banking Jobs
Driver Jobs
Part Time Jobs
Civil Engineering Jobs
Accountant Jobs
Safety Officer Jobs
Nursing Jobs
Civil Engineering Jobs
Hospitality Jobs
Part Time Jobs
Security Jobs
Finance Jobs
Marketing Jobs
Shipping Jobs
Real Estate Jobs
Telecom Jobs

Regulatory Specialist

Job LocationSheffield
EducationNot Mentioned
Salary40,000 - 45,000 per annum
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent , full-time

Job Description

Adecco Lifesciences are working with a long-standing and highly successful Medical Device manufacturer who is looking for a Regulatory Specialist to join the team on a permanent basis.The existing team is already strong and so you will work alongside motivated and experienced RA Specialists supporting the company with Technical File remediation for existing products to ensure compliance to MDR (2017/745) and assist in the creation of technicaldocumentation for new products being introduced in the New Year.Day to day you can expect to:Create and maintain Technical Files in accordance with EC Regulation 93/42/EEC.Transition Technical Files from Medical Devices Directive (93/42/EEC) to Medical Devices Regulation (2017/745)Compile Technical Files and documentation for review by the Notified Body.Provide regulatory support for all post-market surveillance activities.Maintain and approve product labeling to meet regulatory & UDI requirements.Review marketing, promotional material, and website content for regulatory compliance.Manage and maintain global distributors including UK, Europe, Australia, Canada, and USA.Sound like it might be of interestIf you are adaptable, productive and can work well in a team, you will thrive in this position.As you will be working with high-risk devices, experience with Class iii or Orthopeadic devices is essential to understand the complexity of the technical file you are working with.The business strives to offer each candidate continuous professional development and education allowing you to gain further knowledge in the regulatory field and this role is no different allowing you to build on your problem solving, regulatory strategy, lifecycle management and technical file skills.If this role is of interest and you have the relevant experience, then please apply and I will be in touch to talk in more detail.Adecco Lifesciences is acting as an Employment Agency in relation to this vacancy.

Keyskills :
OrthopedicMDRMDDISO13485submissionsTechnical FileRegulatory Specialist

APPLY NOW

Regulatory Specialist Related Jobs

© 2019 Naukrijobs All Rights Reserved