Global Quality Manager

TN United Kingdom; United Kingdom; On-site; GBP 50,000 - 80,000; Full time

Job summary

An established industry player in sustainable healthcare solutions is seeking a driven Global Quality Manager to join their team. This role involves developing and implementing quality assurance strategies aligned with regulatory standards, managing a diverse team of quality professionals, and ensuring compliance with ISO standards. The successful candidate will have a strong leadership background, experience in quality management systems, and a passion for fostering continuous improvement. This is an exciting opportunity to make a significant impact in a growing organization dedicated to improving patient care globally.

Qualifications

• 3+ years experience with ISO 13485 and quality management systems.
• Demonstrated leadership in managing teams and budgets.

Responsibilities

• Develop and implement global quality assurance strategies.
• Lead a culture of superior quality across the business.

Skills

Leadership

Quality Management Systems

ISO 13485

Problem-Solving

Communication

Performance Monitoring

Job description

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Global Quality Manager, United Kingdom ()

Client:

Guided Solutions

Location:

Job Category:

Other

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EU work permit required:

Yes

Job Reference:

0c3fab9038dc

Job Views:

7

Posted:

26.04.2025

Expiry Date:

10.06.2025

Job Description:

Our client is an award-winning leader in sustainable healthcare solutions. They focus on improving the lives of patients and professionals globally through innovative product ranges. Due to significant growth, they are seeking 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 with the procurement team and suppliers to establish and maintain high-quality standards for incoming components and materials.
• Support the Regulatory Lead and cross-functional teams to ensure timely submission of regulatory filings and documentation.
• Lead a culture of superior quality across the business, communicating effectively with all stakeholders to deliver the quality strategy.
• Manage and mentor a diverse team of quality professionals, fostering continuous improvement and excellence.
• 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.

Candidate profile:

• Demonstrated leadership experience, managing people, budgets, and performance.
• At least 3 years of 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.
• Strong problem-solving skills with a track record of successful CAPA initiatives.
• Experience working in a highly commercial environment.
• Ability to collaborate, motivate, and lead across departments on Quality issues, working under pressure to meet deadlines.
• Excellent written communication skills, attention to detail, and ability to summarise effectively.
• Ability to monitor and report performance metrics efficiently.
• UK Driving license and willingness to travel across the UK to manufacturing sites.
• Right to Work in the UK - no Visa sponsorship provided.