4 of 4 Permanent QMS Jobs in Manchester

have competitive holidays and pension contributions... this is the company and the role for you! Your Core Accountabilities * Maintain and control Quality Management System (QMS) documentation, ensuring accuracy, version control, and accessibility. * Coordinate the planning and scheduling of internal and external audits, prepare required documentation, and support follow-up actions … line with company policies and values. Qualifications/Experience * Demonstrable experience in QA administration, documentation control, and supporting audits. * Understanding of quality management systems (QMS), ISO standards, and regulatory compliance. * Strong organisational and administrative skills, with attention to detail. * Effective communication skills for cross-departmental collaboration. * Competence in collating ...

position with genuine ownership in a scaling digital health organisation. Key Responsibilities Quality & Regulatory Leadership Own and maintain the organisation’s Quality Management System (QMS) in line with ISO 13485 Act as the internal lead for the ISO 27001 Information Security Management System (ISMS) Ensure ongoing compliance with HIPAA, DTAC ...

seeking a detail-oriented and organised QA Administrator to support their Quality Assurance team. This role is central to maintaining the Quality Management System (QMS), supporting audits, change management, and continuous improvement activities, while ensuring compliance with company, regulatory, and safety standards. What Youll Do Maintain and control QMS documentation … Your Background Experience in QA administration, document control, and audit support. This could be from markets outside of chemistry. Good understanding of Quality Management Systems (QMS), ISO standards, and regulatory compliance. Strong organisational skills with excellent attention to detail. Confident communicator, with experience working across departments. Experience in a manufacturing ...

business, supporting quality operations across three UK sites : Stockport, Irvine and Warrington. This is a key role responsible for maintaining and developing the Quality Management System, ensuring ongoing compliance with ISO 9001 , and acting as a quality interface with both customers and suppliers. You will report directly … improve ISO 9001 compliance across all sites Manage and support internal and external audits Lead and support APQP activities Ownership and development of the QMS across all three sites Act as the quality point of contact for customers and suppliers Support continuous improvement initiatives within manufacturing Experience/Skills/ ...