Quality Assurance Coordinator

Calibre Scientific Group; Reading; On-site; GBP 45,000 - 65,000; Full time

Job summary

Calibre Scientific Group is seeking an experienced Quality professional to join our Reading site. You will actively maintain and improve the QMS, support regulatory compliance and drive continuous improvement across the business.

You will manage document control, CAPA, nonconformances, change control and risk management, coordinate quality training and monitor KPIs, and work with operations to enhance processes while ensuring compliance and supplier documentation support.

Qualifications

• Experience within an ISO 9001/13485 certified or medical device environment.
• Good understanding of Quality Management Systems and associated processes.
• Experience supporting audits and continuous improvement activities.
• Strong communication, organisational and problem-solving skills.
• Experience with electronic QMS platforms would be advantageous.

Responsibilities

• Maintain and continually improve the Quality Management System (QMS).
• Manage document control, CAPA, nonconformances, change control and risk management.
• Support regulatory and certification audits.
• Coordinate quality training and monitor quality KPIs.
• Work collaboratively with operational teams to improve processes and maintain compliance.
• Support supplier quality assurance and production documentation.

Skills

Quality management

Regulatory compliance

Audits

Continuous improvement

Communication skills

Tools

Electronic QMS platforms

Job description

We're looking for an experienced Quality professional to join Calibre Scientific at our Reading site.

This is a great opportunity to take an active role in maintaining and improving our Quality Management System, supporting regulatory compliance and driving continuous improvement across the business.

• Maintain and continually improve the Quality Management System (QMS).
• Manage document control, CAPA, nonconformances, change control and risk management.
• Support regulatory and certification audits.
• Coordinate quality training and monitor quality KPIs.
• Work collaboratively with operational teams to improve processes and maintain compliance.
• Support supplier quality assurance and production documentation.

What We're Looking For

• Experience within an ISO 9001/13485 certified or medical device environment.
• Good understanding of Quality Management Systems and associated processes.
• Experience supporting audits and continuous improvement activities.
• Strong communication, organisational and problem-solving skills.
• Experience with electronic QMS platforms would be advantageous.

You'll be joining a business where quality, collaboration and continuous improvement are central to what we do.