101 to 125 of 204 Permanent QMS Jobs in England

conformances and collaborate on CAPA objectives. Working with the Leadership Teams as well as building positive and effective relationships with other internal stakeholders on QMS related activities. Ready to apply? This is what you will need to demonstrate; Qualified/Certified Auditor for ISO 13485 (please note, this is a more »

for a perm role on behalf of our client based in Stanford le Hope. Duties and Responsibilities: Maintain the company's Environmental and Quality Management System frame work and ensure ongoing compliance with accredited ISO90001, ISO14001 and any other ISO standards as applicable. Manage day to day operation of the more »

with existing and new requirements. Specify audit scopes to ensure compliance with legislation, industry standards, and company policies. Maintain and enhance the ISO9001 Quality Management System and ISO14001 Environmental Management System. Approve engineering change documents and concessions, and monitor safety performance of fleet personnel and contractors. Ensure depot staff are more »

awards, refer a friend recruitment. This role would suit candidates who have previously worked in roles such as Technical Services Manager, Compliance Manager, Auditor, QMS manager, Quality Systems Manager, Supplier Assurance Manager, Technical Manager. This role is located between Taunton and Exeter just off the M5 more »

any planned equity and debt raises. Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System, compliant with ISO standards. Required skills and qualifications: Prior project appraisal and business planning experience (ideally within renewable energy sector). Experience of project more »

development, and operational efficiency. Directly manage employee appraisals, recruitment efforts, SLA compliance, and round-the-clock support schedules. Key Responsibilities: * Champion our clients Quality Management system, ensuring adherence to procedures and consistently high service levels for our clientele. * Provide proactive and reactive technical support to our customer base, resolving issues more »

or verbally to persons authorised to receive them e.g. Medical, nursing and non-medical staff. g) Is proficient in the use of the Quality Management system, ensuring the effective development and/or management of all controlled documentation, non-conformities and audit reports within the system. h) Ensures quality assurance more »

Essential Significant experience of working in a senior supervisory role in Pathology Desirable Experience working with Pathology IT systems Experience working with a quality management system Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be more »

he administrative aspect of the technical department taking responsibility of the day to day management and maintenance of some or all of the following: QMS, HACCP, legislation, specifications, technical reports, contaminants, complaints, microbiological and nutritional surveillance. Communication - To ensure effective, professional, timely customer communication. Contribute to customer audits and visits more »

prototype algorithmic functions based on data analysis and experimental findings. Additionally, you'll play a role in maintaining adherence to the ISO 13485 quality management system and collaborate effectively with other engineers to support research and development initiatives and the overall project goal – Better patient outcomes! What skills and experience more »

prototype algorithmic functions based on data analysis and experimental findings. Additionally, you'll play a role in maintaining adherence to the ISO 13485 quality management system and collaborate effectively with other engineers to support research and development initiatives and the overall project goal Better patient outcomes! What skills and experience more »

specifications. Maintain cleanliness and organisation in the work environment. Report to Unit Manager promptly regarding any issues or delays. Adhere to company's quality management system and health & safety protocols. Skills & Attributes: Experience in engineering or related field preferred. Proficiency in using precision measuring equipment. Adaptability and quick learning abilities. more »

applications to the post of Digital Forensic Technician. In this role you will support the Technical Manager with the ongoing development of the Quality Management System and technical functions within the Digital Forensics Unit (DFU). You will also assist in the development and maintenance of Technical Standard Operating Procedures more »

knowledge, a minimum of 3 GCSEs. Experience of working in a Biomedical laboratory. Knowledge of computer applications in use within Pathology, particularly LIMS, Quality Management System and Procurement system. High degree of dexterity required Working knowledge of the receipt and preparation of samples for biomedical testing. Desirable Science A Levels more »

ADR Transport Regulations for example). Desirable Specialist Knowledge of MRI Specialist knowledge of UV Experience of teaching and training others Working knowledge of QMS Understanding of HR policies and procedures Skills/Attributes Essential Able to act as a Trust expert in areas of specialist expertise and communicate to more »

the team and with external partners. Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System, compliant with ISO standards PERSON SPECIFICATION Required Experience Good understanding of communications, wiring systems and schematics or equivalent Experience with inspection and testing– C more »

house and contract engineers in Mechanical Engineering Creation and management of product and production Technical Documentation Manage and maintain engineering data within ISO 13485 QMS Engineering management of operations – Design Change, Compliance, Validation etc. Take ownership of engineering drawings and technical documentation relating to technical files Skills, Experience and Education more »

business * Basic recognition of components is desirable, but not essential * Previous experience in an electromechanical production environment is desirable * Working experience of ISO 9001 QMS * A positive, can do attitude more »

will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated departments to ensure work is completed in more »

will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated departments to ensure work is completed in more »

Are you an experienced QMS Administrator looking for a part time role? If so, this interesting and flexible role could be just what you are looking for. The Client Established in the UK in 2000, but originally developed in California, USA, our client designs and manufactures a range of PH … renowned companies who are leaders in their specialised field. The Role They are now looking for an experienced QMS Administrator to ensure the Quality Management System processes are established, implemented and maintained. Key Accountabilities Implement and maintain the companys quality management system (QMS) to ensure compliance with ISO 9001 and more »

Senior Quality Engineer, Quality Manager The Role Reporting into the Quality Manager you will have the following duties: -Supporting the implementation of the quality management system throughout the site. -Maintaining the quality manuals and quality procedures. -Conduct quality system audits and assist in training. -Support and lead process improvements. The more »

QP qualification essential Significant experience working as in a senior quality role within solid dose and none - sterile liquid pharmaceutical settings working and implementing QMS strategies. Significant experience working with cGxP regulations Previous management/supervisory experience in a quality setting Important Information: We endeavour to process your personal data more »

our cutting-edge Medical Imaging Devices. Your tasks will encompass overseeing change management, validation and verification, systems engineering guidance and adherence to our Quality Management System standards. The ideal candidate would be an experienced systems engineer/manager who has experience working on hardware heavy devices. Any experience with optics more »

The role involves coordinating and managing all QA/QC activities to ensure compliance with quality standards and client specifications according to the Company QMS, with appropriate record-keeping. Quality control and assurance of purchased, fabricated, and completed products. Drive to continually improve the standard of quality compliance and awareness more »