Business & Quality Systems Manager
Location: Newcastle upon Tyne (Preferred)
Salary: Competitive
Contract: Permanent
We are on the lookout for a Business & Quality Systems Manager to join the Mayborn family!
The Business & Quality Systems Manager is responsible for providing global management system representation and audit support, to ensure the effective delivery of our Quality Management System.
The Business & Quality Systems Manager will take the lead on coordinating and maintaining ISO certification (9001, 13485, and 14001), to support compliance, innovation, continuous improvement and our brand reputation.
The role will lead on the implementation of the global quality standards, raising awareness and engagement across the business.
In addition, the role holder is responsible for supporting other certification and benchmarking activities to support the successful implementation of Mayborn’s ESG strategy, including Internal Sustainability and Carbon Certification (ISCC) and SEDEX Members Ethical Trade Audits (SMETA).
This specialist role provides technical knowledge of international standards as the frameworks to inform on our governance, process consistency, effectiveness and operational efficiency to support product development, risk management and key business programs.
What you will be doing:
- Leading as the Global Management System Representative our headquarters have effective and robust ISO Management Systems, which are in line with and comply with the requirements of ISO 9001 and 14001.
- Leading as Management System Representative with the Medical Device Management System (ISO 13485), including communications with competent authorities and notified bodies as required.
- Managing, maintaining, and improving our Business Management Systems (BMS) and global approach, supported by our site-based Quality, EHS and Product Compliance Representatives.
- Leading on and coordinating internal audits, documentation control and management reviews activities with internal teams, as required.
- Identifying and driving continuous improvement activities across sites and departments through internal audits, to support both business and customer needs.
- Developing and updating global policies and procedures to meet the requirements of the ISO programs, including the Global Quality Policy, along with new standards and areas where legislative compliance obligations need to be met.
- Lead on managing / keeping up to date a suite of dedicated software applications (Qpulse and Regscan) to manage documents and to monitor & deliver legislative and systems compliance.
- Support in providing Quality inductions.
- Act as the main contact for third-party certification bodies.li>
- Ensure ongoing suitability and effectiveness of the management systems in line with the business’ expanding ISO requirements.
- Using technical ability to develop management system frameworks to deliver any specialist certification schemes, e.g. chain of custody certification schemes (ISCC) and keeping ISCC Hub up to date, to support sustainable and traceable product development and ESG business needs.
- Support on supplier evaluations and external audits to ensure suitability and effectiveness of Mayborn’s supply base with regards to quality, environment, H&S and ESG standards.
- Support on delivering business improvement and management methodology activities, i.e. 6S.
- Manage the central budget in relation to certification and audit costs, working with Legal in relation to contract approvals.
- Support in the coordination, updating and delivery of the business continuity plan and associated risk management activities.
What skills and experiences you’ll need to ace this job:
Essential
- Experience of working in a similar role.
- Certified Lead Auditor (ISO 9001, and 14001).
- Progressive knowledge and experience of implementing Management Systems and change management activities to achieve certification.
- Experience working in a manufacturing environment.
- Educated in a relevant technical area (quality management preferred).
Preferred, but not essential (training will be provided)
- Experience of management representative responsibilities in relation to ISO 13485 (medical devices).
- Knowledge of Carbon Certification (ISCC) and SEDEX Members Ethical Trade Audits (SMETA) or similar.
- Experience of using Q-Pulse Quality Management Information System (QMIS) or similar would be advantageous.
- Understanding of business continuity, resilience and risk management processes.
#J-18808-Ljbffr…