51 to 75 of 204 Permanent QMS Jobs in England

legal & project delivery teams, as required · 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 · Experience of working within a similar senior technical design role, managing multiple projects · Experience in system more »

eg GC, KF, UV-Vis, FT-IR. The use of a Chromatography Data System such as Empower in a regulated laboratory. Significant experience leading QMS driven aspects of a cGMP laboratory, Laboratory error investigation, OOS investigation, Deviation investigation and CAPA. Experience scheduling and planning workloads, resource and equipment including developing more »

compliance with MRP Regulations and AS9100/AS9110 standards by conducting internal audits every 12 months. Quality Management: Establish and maintain a robust quality management system to uphold Our client Fixed Wing approvals to MRP and third-party certified requirements. Supplier Collaboration: Collaborate with Our client Supplier Quality Assurance (SQA more »

with a Life Science Organisation in the search for a Global Head of Quality. Deliverables To lead the build and continual development of the QMS to Quality standards Be the lead SME for Quality & Compliance related issues To shape, provide line management and run the Quality team To hold and more »

Retain knowledge with aviation regulations, including CAA EASA, FAA. First line leader for a team of Quality professionals across multiple locations. Manage the companies QMS and quality systems. Lead continuous improvement of Quality business systems. Manage portfolio of external and customer Quality approvals. Create and conduct internal audit plans covering more »

Significant leadership experience in QA. Expertise in regulations and GMP. Strong managerial and problem-solving skills. QP qualification and relevant degree. Familiarity with electronic QMS systems. more »

Significant leadership experience in QA. Expertise in regulations and GMP. Strong managerial and problem-solving skills. QP qualification and relevant degree. Familiarity with electronic QMS systems. 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 »

an engineering and manufacturing environment designing various valves. You will take responsibility for designing products in accordance with customer requirements ensuring that the Quality Management System is adhered to. *Control valve Design Engineer experience is essential for this role. Design Engineer Key Responsibilities and Specific Accountabilities: Design Engineer Objectives: Follow more »

strong focus on quality, you will guide and manage your team to enhance quality performance. Your main objective will be to strengthen the existing QMS and food safety systems, ensuring compliance with customer and business requirements and legislation. Working cross functionally, you will foster a shared commitment to upholding the more »

requirements and guidelines including IT Infrastructure Library (ITIL), Data Protection legislation, Information Standards, Information Security and compliance with NHS Information Governance. Participate in quality management system, undertaking audits designed to improve IT systems and services. Ensure that there is a proactive and comprehensive approach to risk management and be responsible more »

faults. To update and maintain accurately the medical equipment database. To comply with the requirements of ISO:9001 and ensure the Q-Pulse quality management system and all procedures and protocols are adhered to. Liaise with external companies to obtain information where required to effectively maintain equipment. To identify areas more »

of EMC testing when required. The candidate requires excellent written and verbal communication skills to document their activities in line with the ISO13485 Quality Management System, planning and reporting on their work to a standard suitable for review by regulatory authorities. Skills, Experience & Qualifications: Proven track record in the design more »

human error and of the critical requirement for accuracy in Quality Control of radiotherapy equipment. Knowledge of the NHS working environment within a quality management system (e.g. ISO9001:2015). Comprehension of relevant legislation, national standards, professional and other guidelines, procedures and practices, e.g. ISO 9001:2015, relevant BSI and more »

manuals ' Electrical fault finding ' Electrical safety testing ' Provide technical assistance to service engineering team ' Work within and contribute to the company's ISO9001 quality management system ' Liaise with shop-floor to ensure machines are built to appropriate Company standards ' Assist in commissioning of machines ' Any other duties and responsibilities commensurate more »

inductions and other end user training sessions 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 in an IT service delivery role supporting a Microsoft cloud environment knowledge of Microsoft’s Office 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 »

FID experience (general - Gas Chromatography experience will be considered, to be clear we are looking for someone who has commercial lab experience working to QMS like UKAS 17025 or GLP/GMP/BRC) or GC/MS experience Strong interpersonal, organisation skills Able to work towards deadlines Good IT more »

with regulatory standards, maintaining quality systems, and supporting continuous improvement initiatives. Responsibilities: Support the implementation and maintenance of the company's Quality Management System (QMS) in accordance with regulatory requirements. Assist in conducting internal audits to assess compliance with GMP/GDP standards and company policies. Participate in the review more »

Management of the destructive and non-destructive testing activity. Management and control of the product and system auditing. Management and control of all relevant QMS systems ISO9001, ISO14001 etc.. Lead and manage the development of preventative/corrective actions. Manage proactively any technical queries with customers providing all necessary guidance. more »

opportunity with a clinical-stage biopharmaceutical company with multiple Phase 3 assets.Key Responsibilities:To play a key role in maintaining and monitoring the GxP QMS ensuring it meets all regulatory requirements and standards, with emphasis on GCP compliance.To provide support and advice to Clinical Development teams with regards to:Definition more »

Quality Engineer Lead , Scientific Instrumentation Our client is looking to recruit a Quality Engineer Lead responsible for: Maintaining ISO accreditation and improving the quality management system performance Supporting a reduction in supplier quality problems and non-compliance on shop floor quality Assisting in the development and implementation of good fit more »

the administrative aspect of the Technical Department taking responsibility for the day to day management and maintenance of some or all of the following; QMS, HACCP, legislation, specifications, Technical Reports, Contaminants & Non Conformance Logs, complaints, microbiological & nutritional surveillance, this work includes data entry, trending, filing, information requests, co-ordination of more »

errors and reduce overall cost of Quality Monitor output, quality & scrap rates. Improving OTD performance Maintain records of products and approved suppliers Continually improve QMS processes If you are interested in this position, please apply with an up to date CV as soon as possible, along with your availability and more »

compliance with quality standards. Preferred Requirements: Experience in assembly processes and quality control. Skilled in conducting comprehensive audits and implementing safety measures. Proficiency in QMS and ISO systems to drive quality enhancements. Excellent understanding of quality engineering principles and practices. Demonstrated ability to identify and resolve quality-related issues. Preferred more »