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Quality Manager Consultant

RQM+London, United KingdomOnsite
This job is no longer open
As a Quality Manager, you will be responsible for developing and improving Quality systems in compliance with requirements through auditing, gap assessment, remediation and including management and support of Corrective/Preventive actions, Recall, Complaints etc.    

Key Responsibilities


  • Develop/contribute to Quality System development: ISO 13485, QSR, MDSAP, 21 CFR 820, GMP 
  • Improve/remediation Quality systems through development and or revision of elements of the QMS to meet standards or new requirements Usability, ISO 13485:2016, EU MDR, GMP, safety risk management, 60601-1 3rd edition)
  • Write/improve and train others on SOPs
  • Perform gap assessments to prepare for external audits/FDA inspections
  • Support external audits 
  • Coordinate and conduct internal audits
  • FDA inspection readiness and support
  • Conduct EU MDR mock NB audits
  • Coordinate and conduct Supplier quality audits
  • Select and qualify suppliers
  • Create/Maintain Authorize Supplier List (ASL) or scorecards
  • Draft Supplier Agreements 
  • Train others on Supplier Quality 
  • Develop SOPs for Supplier Quality 

Key Requirements


  • Bachelor’s Degree in relevant subject   
  • Experience working within medical/diagnostic device in a quality role in industry
  • Working knowledge of requirements such as 21 CFR 820, ISO 13485 and GMP
  • Working knowledge of standards such as: ISO 13485:2016, EU MDR, GMP, safety risk management, 60601-1 3rd edition
  • FDA Regulatory requirements, the EU Medical Device  
  • Experience with MDSAP audits 

Being an industry leader in regulatory and quality consulting is just the beginning for RQM+. We consider our employees our biggest asset and we invest heavily in ongoing learning and development. Providing a rewarding place to work is rooted deep in our core values. From an industry leading compensation package to a deeply engrained focus on work life balance, RQM+ has a unique offering for regulatory and quality professionals. At RQM+, you are not just another employee, you are a member of RQM+ family.

Make your impact today!We invite you to apply if you have an interest in learning more about our organization and beginning your journey with us.Job Opportunity VerificationAt RQM+, we prioritize the security of our job applicants. To ensure a safe application process:All legitimate RQM+ job opportunities are listed on our official careers page: rqmplus.com/careersEvery candidate going through the interview process will participate in a voice and/or video interview.Exercise caution with unsolicited job offers or requests for sensitive information.Apply for this job

This job is no longer open

Life at RQM+

R&Q and Maetrics have merged to become RQM+, the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. The integration of our leadership teams and extensive skills and experience of our collective resources have created a highly agile, scalable, and global organization. Learn more about our services, free resources, and more at RQMplus.com
Thrive Here & What We Value1. Industry Leader in Medtech2. Ongoing Learning and Development for Employees3. Rewarding Place to Work4. Unique Offering for Regulatory and Quality Professionals5. Member of RQM+ Family
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