Quality Assurance Manager in Romsey, Hampshire

Quality Assurance Manager in Romsey, Hampshire

Romsey Full-Time No working from home possible
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At a Glance

  • Tasks: Lead quality assurance and ensure compliance in the medical device industry.
  • Company: Dynamic company in Romsey focused on quality and regulatory excellence.
  • Benefits: Competitive salary, hands-on leadership role, and opportunities for continuous improvement.
  • Other info: Join a culture of quality with excellent career growth potential.
  • Why this job: Make a real impact in healthcare by championing quality and compliance.
  • Qualifications: Experience in Quality Assurance within the medical device sector is essential.

Job Title: Quality Assurance Manager
Location: Romsey (On-Site Working)
Salary: £60,000 - £70,000 (Depending on Experience)

Please Note: All Applicants must have the right to work in the UK without the need for VISA sponsorship now or in the future

Overview

A successful candidate will act as the Quality Management Representative, reporting to senior leadership and ensuring the ongoing effectiveness, compliance, and continuous improvement of the Quality Management System (QMS).

They will provide expert guidance across product development, manufacturing, and operational teams to maintain compliance with applicable medical device regulations and quality standards.

This hands-on leadership role will champion a culture of quality, regulatory excellence, and continuous improvement across the organisation.

Key Responsibilities

  • Lead the Quality Assurance function and drive quality and regulatory compliance across the organisation.
  • Maintain and continuously improve the Quality Management System (QMS) to meet applicable regulatory and industry standards.
  • Act as the Quality Management Representative and ensure ongoing regulatory compliance and audit readiness.
  • Promote a culture of quality, risk management and continuous improvement across all business functions.
  • Lead CAPA, internal audits, supplier quality and external audit activities.
  • Monitor quality performance, analyse trends and implement improvement initiatives.
  • Provide quality and regulatory support throughout product development, manufacturing and operational activities.
  • Develop, coach and lead the Quality team while maintaining effective relationships with regulators, customers and external stakeholders.

Required Skills & Experience

  • Proven experience in Quality Assurance within the medical device industry.
  • Strong knowledge of medical device design, development and Quality Management Systems (QMS).
  • Working knowledge of ISO 13485, FDA 21 CFR Parts 820 & 11, and EU MDR (2017/745).
  • Experience leading internal, external and regulatory audits.
  • Understanding of risk management principles (ISO 14971 desirable) and regulatory compliance requirements.
  • Proven ability to lead CAPA and root cause investigations using recognised problem-solving methodologies.
  • Experience driving continuous improvement and implementing quality improvement initiatives.
  • Strong leadership, communication and stakeholder management skills, with the ability to influence cross-functional teams.
  • Excellent analytical, organisational and project management skills, including supplier and customer quality management

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Quality Assurance Manager in Romsey, Hampshire employer: Energy Jobline CVL

Join a well-established property maintenance contractor in Birmingham, where you will enjoy a supportive work culture and the opportunity for career progression. With benefits such as a company van, fuel card, and ongoing training, this role not only offers stability but also the chance to develop your skills in a hands-on environment backed by an experienced office team. Experience a rewarding career with guaranteed annual leave and social events that foster a strong team spirit.

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Contact Details:

Energy Jobline CVL Recruitment Team

We think you need these skills to ace Quality Assurance Manager in Romsey, Hampshire

Quality Management Systems (QMS)
ISO 13485
FDA 21 CFR Parts 820 & 11
EU MDR (2017/745)
Internal Audits
External Audits
Regulatory Compliance