Regulatory Affairs Manager

Location

Remote, UK

Job Type

Company Overview

LumiraDx is a medical technology company developing, manufacturing and marketing smart connected diagnostics and diagnostic-led care solutions. Founded in 2014 by entrepreneurs with a successful track record in building and scaling medical diagnostics and health IT businesses, the company has major operations in the UK and the USA, and is supported by a global sales network, LumiraDx is a high growth organisation. We have recently launched the innovative LumiraDx Platform, and are looking for proactive, experienced, focused and enthusiastic individuals who can make a significant contribution to the continued growth and success of our dynamic and forward-looking company.

Role & Responsibilities

Regulatory Affairs Manager - this role can be remote based but with regular travel to our sites in Scotland 

The Opportunity

Activities such as requirements generation document/process creation, review and approval of documents and working with all project teams to guide the teams in the day to day development and to ensure applicable standards and regulations for the products being brought to the market are incorporated throughout the development. 

Reporting to the LumiraDx  Quality and Regulatory Director, the successful candidate shall be responsible for the regulatory activities for the legal manufactured products associated with  IVD medical devices (assays, instruments, software and ancillary items relating to the system) development through the R&D phase and the verification and validation phase through launch and any support required by the business for on market regulatory issues.  

The Role

  • Management or regulatory dossiers of all legal manufactured products for pre market
  • Management and Creation of QA/RA plans for the design and development teams to support Global markets up to the formation of the standard dossier.
  • Creation and maintenance of harmonized standards compliance plans
  • Creation and maintenance of regulatory procedures to align with Global requirements
  • Management of regulatory process relating to marketing collaterals and country localization process
  • Review and approval of Labelling and marketing collaterals
  • Lead and manage a team of Regulatory Specialists working in pre market environment, including day to day activities to support the business in accordance with pipeline plans and non routine activities as required by the business.
  • Support the training and development needs of the team
  • Provide training for other areas of the business on regulatory process and other compliance activities.

Required Experience

About You:

We are looking for a highly motivated individual with exceptional attention to detail and high level of skills in communication, along with the following skills and experience:

  • Knowledge and experience of working to the appropriate quality and regulatory standards including ISO 13485, ISO 14971, FDA 21CFR part 820, IVD 98/79/EC/IVDR
  • Development and writing of CE marking technical files
  • Knowledge of Clinical process
  • Experience and knowledge of vertical and horizontal standards for IVD medical device instruments, software and assays in the point of care.
  • Previous experience in people management is highly desirable
  • Excellent organizational skillsInfluence internal project team and external parties to maximize success opportunities
  • Demonstration of good problem solving abilities
  • Strong communicator
  • Experience of working in an IVD or medical device design and manufacturing environment
  • Development and writing of CE marking technical files

 

For further information and to apply for this role, please click APPLY

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Thank you for your interest. If you're successful in your application, you may be subject to all or some of the LumiraDx standard pre-employment checks. This includes employment references; Criminal records data checks which are processed as part of our recruitment process for employment or continued employment to comply with legal and regulatory obligations to which the company is subject. LumiraDx place a high level of importance on its responsibilities for information security and privacy and have put in place an information security management system to ensure that the company and its staff maintain the highest standards with respect to data protection and information security.