Global Quality Manager

Guided Solutions; United Kingdom; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading company in sustainable healthcare solutions is seeking a Global Quality Manager to drive quality assurance strategies and ensure compliance with regulatory standards. The role involves managing a team, collaborating with stakeholders, and enhancing quality management systems across the organization.

Qualifications

• Minimum of 3 years experience assessing AQL and implementing quality management systems aligned with ISO 13485.
• Experience with Class 1 and Class 2 Medical Devices.
• Strong problem-solving skills.

Responsibilities

• Support development and implementation of global quality assurance strategies.
• Manage and mentor a diverse team of quality professionals.
• Ensure compliance with ISO 13485/9001 standards.

Skills

Leadership

Problem-solving

Collaboration

Attention to detail

Job description

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Global Quality Manager, United Kingdom ()

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Client:

Guided Solutions

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

0c3fab9038dc

Job Views:

6

Posted:

02.06.2025

Expiry Date:

17.07.2025

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Job Description:

Our client is an award-winning leader in sustainable healthcare solutions. They are focused on helping improve the lives of patients and professionals on a global scale through their innovative product ranges. Due to significant growth, they are looking for a driven Global Quality Manager to join their team.

Key responsibilities:

• Support the development and implementation of global quality assurance strategies, policies, and procedures aligned with regulatory standards (e.g., ISO 13485 & 9001).
• Evaluate the suitability of current distributors and recommend replacements if needed.
• Collaborate and advise the procurement team and suppliers to establish and maintain high-quality standards for incoming components and materials.
• Support the Regulatory Lead and other cross-functional teams to ensure timely submission of regulatory filings and documentation.
• Lead the culture of superior quality across the business, communicating with all stakeholders to professionally deliver the quality strategy.
• Manage and mentor a diverse team of quality professionals, fostering a culture of continuous improvement and excellence.
• Evaluate and maintain robust quality management systems to support product development, manufacturing, and distribution processes.
• Ensure compliance with ISO 13485/9001 standards throughout all stages of product development, manufacturing, and distribution.

To be considered for this position candidates must closely match the following reference profile:

• Demonstrated leadership experience, managing people, budgets, and performance.
• A minimum of 3 years experience assessing AQL and implementing quality management systems aligned with ISO 13485.
• Experience working with Class 1 and Class 2 (sterile and non-sterile) Medical Devices in accordance.
• Strong problem-solving skills with a track record of implementing successful CAPA initiatives.
• Experience of working in a highly commercial environment.
• Ability to collaborate, motivate, and lead across departments on Quality issues. Working under pressure to meet deadlines.
• Strong written communication skills, excellent attention to detail with the ability to summarise effectively.
• Ability to efficiently monitor and report performance metrics.
• UK Driving license and ability to travel across the UK to manufacturing sites.
• Right to Work in the UK - This role does not offer Visa sponsorship.