26 to 50 of 144 Permanent QMS Jobs in England

team. Internally will liaise with Team Leaders & Quality Manager. QUALIFICATIONS and PERSONAL PROFILE Must have Industry Standard Inspection Qualifications (IPC). Awareness & understanding of QMS Disciplines IAW BS EN ISO 9001:2008 & AS EN 9100. Awareness & understanding of ESD Controls. Reading & understanding Complex Engineering Drawings & Instructions. Key personal skills:- Excellent more »

required in Quality Engineering in a manufacturing environment Role: Reporting to the Senior Quality Lead, you will be responsible for all aspects of Quality, QMS, Continuous Improvement and Business operating systems and play a key role in the day-to-day quality operations at our UK factory in Slough. The more »

the authority's expectation. The role holder will perform all duties required of a Quality Director, provide leadership to the Quality Teams, improve the QMS, provide expertise and guidance on changing regulatory landscape and input in operations that protects company reputation whilst maintaining product supply to market. The role holder more »

and effluent batches. Monitoring trends in data and reporting any issues directly to Quality Management. Assist Quality Manager in the maintenance of the Quality Management System as required. Reporting and managing of data on trends or certain batches declining if applicable, product quality and comms. Writing SOP and risk assessments. more »

production of bespoke military vehicles. Day-to-day, you'll be responsible for providing assurance at all levels of the business that the quality management system and associated policies and processes have been effectively implemented. Responsible for maintaining the audit programme including all internal, external and joint audits Produce quality more »

is required. You will need to be conversant with the main laboratory information management system, and with middle-ware packages. There is a quality management system to ISO 15189 standards, within which you will be required to operate, particularly getting involved in audit and the investigation of adverse occurrences. The more »

improvement projects Desirable but not essential skills to have would be: RCA (Root cause analyses techniques) Previous experience in a Pharma environment Exposure to QMS - CAPA's, CC, RCA etc Experience on all mainstream software packages including but not limited to Siemens, Allen Bradley and Mitsubishi. Medium to High manufacturing 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 (e.g. ISO14001:2018, Lead the creation and more »

an experienced Quality Assurance Manager with food manufacturing experience. My client are keen to engage a candidate who has experience of managing a quality management system in a food manufacturing facility, candidates should have experience of managing a quality team, leading on audits, working on customer complaints and should have more »

all quality data is accurate and up to date. Implement quality control and assurance procedures to ensure that QA processes meet the companies established QMS and certification requirements. Assist senior management in preparing for and participate in external audits and regulatory inspections related to quality. As a successful candidate you more »

the regulatory requirements of Annex 1 EU GMP. Lead Responsibility for the maintenance of all aspects of the aseptic units reactive and proactive quality management system Lead Responsibility for the release of aseptically prepared products, the department has an annual workload of up to 50,000 items. Lead Responsibility for 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 »

define process parameter to ensure process capability 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 to find out more, along with your availability and more »

and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a related field. Minimum of more »

plant Business Management System. Support the roll out of the Business Systems strategic improvement business plan. The maintenance and development of the companys quality management system documentation, including control and supervision of all amendments and revisions. Work effectively within various business units both in house and externally to improve the more »

and National Office Requirements.o Business and contract planning, including management of SLA's.o Cost reduction plan/Cost Improvement Plan management and delivery.o Quality Management System and Right Result. About us There's never been a more exciting time to build your career at Frimley Health, one of the country more »

Quality Control of Radiotherapy Equipment Treatment Planning of Radiotherapy Patients Experience with complex computing systems and basic Microsoft Office skills Working within a quality management system Skills Essential Ability to use complex computerised Ability to use complex computerised Treatment Planning Systems and a range of radiotherapy equipment Computer literate Highly more »

Radiographic standards within the service ensuring that staff have the opportunity to assess their own performance on a regular basis. To maintain the quality management system to continually improve best practice. To take responsibility for providing a clean and safe environment within your area of work. To consistently carry out 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 »

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 »

that arise as quickly and efficiently as possible to prevent compromising quality and safety standards. Ensure compliance and assist with adherence to the Quality Management system (ISO9001/AQAP2110) Report on Key Performance Indicators (KPIs) in order to adhere to process and prevent occurrence of any non-conformity relating to 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 »

Systems (CDS), Laboratory Information Systems (LIS), Bioinformatics Software, Statistical Analysis Software, Image Analysis Software, Chemical Inventory Management Software, Lab Automation Software, Quality Management Software (QMS), Environmental Monitoring Software, Programmable Logic Controllers (PLCs), Distributed Control Systems (DCS), Supervisory Control and Data Acquisition (SCADA) systems, Human-Machine Interfaces (HMIs), Industrial Control Systems more »

parent company for Eyelit, MESTEC and Optessa who are leaders in Manufacturing Execution (MES), Advanced Planning and Scheduling (APS), Manufacturing Operations (MOM), Quality Management (QMS) and Factory Automation solutions. Eyelit Technologies has delivered unmatched results for a global customer base in the manufacturing industry using cutting edge technology and advancements more »