Full-Time

Quality Assurance Specialist

Resonant Clinical

Resonant Clinical

No salary listed

Chorley, UK

Hybrid

Two days per week in the office are required.

Bachelor's

Category
QA & Testing (1)
Required Skills
Microsoft Office
Six Sigma
ISO 9001
Word/Pages/Docs
Quality Assurance (QA)
Excel/Numbers/Sheets
Microsoft Outlook
PowerPoint/Keynote/Slides
Requirements
  • Experience supporting or managing Quality Management Systems within a regulated environment.
  • Strong knowledge of quality standards and regulations, including ISO 9001, ISO 13485, FDA Quality System Regulations (21 CFR Part 820), and similar regulatory frameworks.
  • Experience conducting internal audits and supporting customer, supplier, or regulatory audits.
  • Knowledge of corrective and preventive action processes, complaint handling, non-conformance management, and root cause analysis methodologies.
  • Strong documentation control experience, including standard operating procedure development, review, and implementation.
  • Problem-solving and analytical skills to identify trends and drive improvements.
  • Experience working with quality software systems and electronic Quality Management Systems.
  • Communication and stakeholder management skills, with the ability to influence at all levels of the organisation.
  • Organisational skills and the ability to manage multiple priorities and deadlines.
  • Proficiency in Microsoft Office applications, including Word, Excel, Outlook, and PowerPoint.
  • Ability to work independently while collaborating effectively within cross-functional teams.
Responsibilities
  • Support the management and continuous improvement of the site's Quality Management System, including the Quality Manual, standard operating procedures, work instructions, forms, and associated documentation.
  • Lead the implementation, revision, and control of quality system documentation to ensure compliance and operational effectiveness.
  • Manage and support the corrective and preventive action programme, including investigation, implementation, effectiveness review, and closure of corrective and preventive actions.
  • Plan, conduct, and lead internal audits in accordance with ISO 9001, ISO 13485, Quality System Regulation, and other applicable standards.
  • Support customer, supplier, and regulatory audits, including audit preparation, responses, corrective actions, and closure activities.
  • Coordinate supplier quality activities, including supplier evaluations, performance reviews, and supplier audit programmes.
  • Support complaint investigations, including review, escalation, resolution, and closure in line with quality requirements.
  • Monitor quality trends and performance metrics, identifying opportunities for continuous improvement and risk reduction.
  • Lead or support Lean, Six Sigma, Kaizen, and other continuous improvement initiatives to strengthen quality systems and operational performance.
  • Support validation activities, including preparation and execution of protocols, testing, and documentation where required.
  • Drive the implementation and optimisation of quality management software systems, including ETQ Reliance modules and related tools.
  • Deliver training and guidance on quality processes, compliance requirements, and continuous improvement methodologies.
  • Evaluate emerging regulations, standards, and industry best practices, providing recommendations to support ongoing compliance and business readiness.
  • Collaborate cross-functionally with Operations, Supply Chain, Customer Service, and Leadership teams to promote a culture of quality and continuous improvement.
Desired Qualifications
  • Previous experience within medical devices, pharmaceuticals, biotechnology, clinical trials, healthcare, or other GxP-regulated industries.
  • Lead Auditor qualification or formal auditing certification.
  • Experience with ETQ Reliance or other electronic Quality Management Systems.
  • Knowledge of EU MDR (745/2017) and IVDR (746/2017) regulations.
  • Lean Six Sigma Green Belt certification or experience applying Lean, Six Sigma, or Kaizen methodologies.
  • Experience supporting validation programmes and qualification activities.
  • Experience managing supplier quality programmes and supplier audits.
  • Project management experience, particularly within quality or compliance-focused initiatives.
  • Experience supporting global quality or regulatory compliance programmes.

Company Size

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Company Stage

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Total Funding

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Headquarters

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Founded

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