1 to 25 of 244 QMS Jobs in England

ensuring timely and accurate responses. Contribute to the supplier qualification processes, including conducting supplier audits and assessments to evaluate supplier capabilities. Maintenance of the QMS: Contribute to the creation, maintenance, and organisation of quality-related documentation , including SOPs, work instructions, quality manuals, records and training material. Establish key performance indicators … Experience Degree in a relevant area of studies. 2 - 3 years experience in the role out of Quality policies. Knowledge of Quality Management Systems (QMS). Proven Auditing Skills. Continuous Improvement Mindset. Excellent interpersonal, verbal, and written communication skills. Experience of working at the headquarters of an international company. Fluent more »

document control and the ability to implement robust document control processes while working closely with the Head of Quality and Regulatory Affairs establish the QMS aligned with ISO 13485 requirements, driving continuous improvement and operation excellence. The successful candidate will also compile technical files with comprehensive documentation to support regulatory … processes Maintain compliance throughout the product lifecycle Assist with the development of comprehensive technical files for CE marking Collaborate with stakeholders to establish a QMS Quality and Regulatory Specialist Requirements: Bachelor's degree in a relevant field (e.g., Engineering, Life Sciences, Regulatory Affairs) 2 years' experience in quality and regulatory more »

compliance with ISO 13485, UK MDR 2002, MDR 2017/745, MDD 93/42/EEC, MDSAP, and other regulations. Prepare and maintain QMS and regulatory documentation. Assist QA Admin team with product approvals for UK and international markets. Evaluate suppliers and conduct approval audits. Document quality audits to … in a production/manufacturing environment. Internal and external quality auditing experience to ISO 13485. Passion for quality excellence. Previous quality assurance experience, including QMS documentation. Knowledge of CAPA and root cause analysis tools. Practical problem-solving approach. Understanding of ISO 14971 quality risk management principles. Self-motivated and team more »

management of employee performance, absence management, and management of rostering Accountability for the clinical safety of the transfusion service, and operation of the quality management system, including compliance with the Blood Safety and Quality Regulations 2005 (as amended) and BS EN ISO 15189:2012 Liaison with the client, Mid and more »

control of quality documents (SOPs, WIs, records etc) Management Representative responsible for ISO 14385 certification and maintaining the effectiveness of the Full Support Healthcare QMS Maintenance and communication where required of technical documentation Investigate and report on non-conformances, customer complaints and CAPA issues within specified timeframes Validation of sterilisation … deadlines. Must be adaptable, numerate, literate and be willing and quick to learn with the desire to succeed Knowledge and practical experience of using QMS software (Q-Pulse desirable).Job Offer Highly negotiable basic salary. Other benefits. Please contact Natalie Hudson at Michael Page Birmingham more »

Quality Management System Lead Permanent Reading - Hybrid working Context: The People team are accountable for the management, welfare and wellbeing of all employees working within MBNL, that enable Three and BT-EE to deliver best customer experiences. The Health, Safety, Quality and Environment team, working within the People team, is … standards, specifically ISO9001 and ISO45001. What you will do: Be responsible for the implementation and ongoing management of an integrated health, safety and quality management system aligned to ISO45001:2018 and ISO9001:2015 requirements, potentially widening to other management system standards over time (e.g. ISO14001:2018, Lead the creation and more »

have a wide range of responsibilities, from operational tasks like batch review and production liaison to broader activities such as auditing, supplier management, and QMS implementation. Crucially, you'll also serve as Deputy QA Manager, with some immediate line management duties and close collaboration with the QA Manager to meet more »

and prepare comprehensive reports in accordance with design control standards. Background in the medical device sector to understand regulatory requirements and quality management systems (QMS) essential for successful product development. (ISO13485) Knowledge in mechanical engineering with a focus on testing equipment and innovation in product development. Requirements: Bachelor's degree more »

Specialist to join them. As the new QARA Specialist, you will work closely with the QA & RA Managers to develop and manage the existing QMS and work closely on the implementation and transition to an eQMS. Alongside this you will be heavily involved in CAPA & NCR processes, SOP creation, auditing … background in In Vitro Diagnostics or Medical Devices. You will have strong experience in the management and/or implementation of an ISO 13485 QMS, CAPA processes and auditing. Key Responsibilities: Develop and Maintain ISO 13485 QMS Support the implementation and transition to an eQMS Creation and implementation of SOPs … technical field Proven experience in the IVD or Medical Device Industries Proven experience in the maintenance and/or implementation of an ISO 13485 QMS Proven experience and knowledge of CAPA Process and Auditing Auditing certification is highly advantageous If you have the necessary skills and experience to be successful more »

ensuring timely and accurate responses. Contribute to the supplier qualification processes, including conducting supplier audits and assessments to evaluate supplier capabilities. Maintenance of the QMS: Contribute to the creation, maintenance, and organisation of quality-related documentation , including SOPs, work instructions, quality manuals, records and training material. Establish key performance indicators … Experience Degree in a relevant area of studies. 2 - 3 years’ experience in the role out of Quality policies. Knowledge of Quality Management Systems (QMS). Proven Auditing Skills. Continuous Improvement Mindset. Excellent interpersonal, verbal, and written communication skills. Experience of working at the headquarters of an international company. Fluent more »

or exceeding of SLAs and KPIs. Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System (compliant with ISO 9001 and 14001). PERSON SPECIFICATION Required skills and experience ERP Systems Expertise: In-depth knowledge and understanding of Dynamics more »

Ideally a qualified, certified Project Manager. Overview: Own ISO 9001 Plan Responsibilities, Policies, and Objectives of the Project Your Project Documentation to Launch Quality Management System Performance for Certification Improvement activities Key Responsibilities – Project Manager Quality Systems Health and Safety in the workplace above everything else, leading by example and more »

to management meetings. Committed team player. Able to work in a flexible, and occasionally highly demanding work environment. Awareness of a Quality Management System (QMS) Previous Military experience of benefit. Job Reference Number 15288BR Employee Type Full Time Hours Per Week 37.5 Working Schedule 4xFlex Country United Kingdom (UK) Clearance more »

levels of GMP, food safety and integrity standards. Responsibilities Include: • Supporting the overall technical strategy, tactics, policy & plans • Responsible for the company’s quality management system to ensure compliance with standards and (HACCP) procedures on food handling • Coordinate all quality assessment and laboratory activities • Ensure that both inbound and outbound 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 »

of RCA tools such as 8D, 5WHY, ISHIKAWA, FMEA’s Champion and support the team of procedures, working instructions and SOP’s Maintaining ISO9001 QMS and implementing TQM Monitor output, quality & scrap rates. Improving OTD performance Maintain records of products and approved suppliers Continually improve QMS processes If you are more »

for Daily Management of the Functional team and their performance; Leads people using company values and core behaviors with a GEMBA presence. Maintain Quality Management System in accordance with Corporate, BU and regulatory requirements advocating complainant change management. Leads and implement strategic initiatives to reduce the number of internal and more »

to work within the quality assurance team based in Manchester. The QA Specialist will ensure the maintenance and continuous improvement of the company quality management system (Q-Pulse). Key areas of responsibility: Perform product releases by reviewing and approving products or services, ensuring they meet established quality standards. Collaborate … in the development, implementation, and enhancement of QMS documents and processes to ensure compliance with quality standards. Assist in completing activities and maintaining records within the QMS related to Nonconformities and Corrective Actions, ensuring timely resolution and documentation. Support the supplier management process by evaluating suppliers, conducting audits, and ensuring … in the management of equipment used in QA processes, ensuring proper maintenance and availability. Conduct internal audits as required to assess compliance with the QMS, identify areas for improvement, and implement corrective actions. Provide training and support to users of the QMS, ensuring understanding and adherence to established procedures. Generate more »

The Company A world-leading manufacturer looking for a QA Technician to join the team. The Role As a QA Technician, your primary responsibility will entail conducting routine incoming material inspections, managing material transactions within the Enterprise Resource Planning (ERP more »

safety legislation and standards. • Develop and monitor Leading & Lagging KPIs in collaboration with the Site Management Team. • Provide support for food safety and quality management system auditing at selected third-party pack sites. • Act as the Site Lead on Pest Management. • Actively support site hygiene management systems, ensuring effective chemical more »

compliance with ISO 13485, UK MDR 2002, MDR 2017/745, MDD 93/42/EEC, MDSAP, and other regulations. Prepare and maintain QMS and regulatory documentation. Assist QA Admin team with product approvals for UK and international markets. Evaluate suppliers and conduct approval audits. Document quality audits to … in a production/manufacturing environment. Internal and external quality auditing experience to ISO 13485. Passion for quality excellence. Previous quality assurance experience, including QMS documentation. Knowledge of CAPA and root cause analysis tools. Practical problem-solving approach. Understanding of ISO 14971 quality risk management principles. Self-motivated and team more »

particularly Mercurial. Typhoon domain knowledge, particularly cockpit Human Machine Interface (HMI). Desirable: Knowledge and experience of Linux. Experience in Task Leading duties, including QMS documentation. Avionics/Mission systems domain knowledge. Use of Jira to manage software tasks. Knowledge of Simulation Interoperability (HLA/DIS/Link16) and associated more »

Our client have an exciting opportunity for a Quality Assurance Operative to join the team within the Barnsley factory. The ideal candidate must be flexible with working hours, and ideally hold a full UK driving licence. You will join them more »

standards, specifically ISO9001 and ISO45001. What you will do: Be responsible for the implementation and ongoing management of an integrated health, safety and quality management system aligned to ISO45001:2018 and ISO9001:2015 requirements, potentially widening to other management system standards over time (eg ISO14001:2018, Lead the creation and more »

milestone progress to the Project Lead, Programme Manager and Stakeholders. Maintain best practices within the Software Team, ensuring technical journals, essential research and company QMS process are followed. Leadership and administration of the Sprint process for the Software Team. Support the delivery of product firmware and software within the Software more »