Instrumentation Quality Engineer

Location

Manor Loan, Stirling

Job Type

Permanent

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 currently has over 700 employees worldwide. 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

Opportunity:
Reporting to the Lumira Dx Quality and Regulatory Director, the successful candidate shall be responsible for the day to day Quality Management System activities associated with In Vitro Diagnostic instrumentation and software throughout the product lifecycle including the Research and Development phase the verification and validation phase, manufacturing and product release. Activities such as document/process creation, review and approval of documents and working with all project teams to guide the teams in the day to day use of the quality management system and to ensure applicable standards and regulations for the products being brought to the market are incorporated throughout the lifecycle.
 
Key Roles and Responsibilities:
  • Quality representative for project teams throughout product lifecycle and product realization activities
  • Creation and management of documentation forming the Design History File and Device Master Record.
  • Assess, control and coordinate changes to Design History File and Device Master Record.
  • Coach and support in the writing of design requirements and specifications.
  • Coach and support in the writing of Verification and Validation plans and protocol.
  • Creation of traceability matrices.
  • Organize, host and facilitate risk management related activities and design reviews with the project teams and ensure compliance of such activities to the applicable standards and regulations.
  • Ensure compliance of documentation for design partners (and suppliers) within the supply chain.
  • Support supplier approval and monitoring activities.
  • Prepare and create documents and records for upload on to GAS.
  • Review and approve as Quality representative on project teams and QMS.
  • Review and approve Device History Records and final product release.

Required Experience

Essential skills:
  • Knowledge and experience of working to the appropriate quality and regulatory standards including ISO13485, FDA 21CRF Part 820.
  • Experience of working in an In Vitro Diagnostic or medical device environment with a strong quality focus and at minimum 2 years’ experience through development and verification and validation activities.
  • Knowledge and experience in electromechanical medical device Hardware and software projects
  • Excellent organizational skills for working on multiple projects.
  • Ability to use problem solving tools and methodologies.
  • Influence internal project team and external parties to maximize success opportunities.
Desirable skills:
  • Specific experience, science degree desired.
  • Continual Improvement mindset (PDCA, Kaizen, Six Sigma, Lean, Value Stream Mapping)

 

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

APPLY

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.