Quality Manager Consultant

Posted Yesterday
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London, Greater London, England
3-5 Years Experience
Healthtech
The Role
Responsible for developing and improving Quality systems in compliance with requirements through auditing, gap assessment, remediation, and management of Corrective/Preventive actions. Key responsibilities include contributing to Quality System development, improving Quality systems, conducting audits, and supporting regulatory inspections. Requires a Bachelor's Degree and experience in the medical/diagnostic device industry with knowledge of quality standards and regulations.
Summary Generated by Built In

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 Verification

At 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/careers

Every 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.

Top Skills

Gmp
Iso 13485
Mdsap
Qsr
The Company
Monroeville, PA
508 Employees
On-site Workplace

What We Do

RQM+ is the world’s leading provider of regulatory, clinical and quality solutions to the MedTech industry. We deliver transformative solutions to customers by providing unrivaled collective knowledge and expertise, fueled by our passion for customer success. Our experts are collaborative, laser-focused on customer needs, and committed to delivering high-value solutions for both medical devices and diagnostics that exceed expectations.

Learn more about our services, free resources, and more at www.RQMplus.com

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