76 to 100 of 275 QMS Jobs

importance and benefits of quality procedures A strong analytic approach & detailed understanding of quality tools and proceses Good understanding of ISO9001 or similar quality management system Experience of continuous improvement methodologies To apply for this role or to be considered for further roles, please click "Apply Now" or contact Sarah more »

importance and benefits of quality procedures A strong analytic approach & detailed understanding of quality tools and proceses Good understanding of ISO9001 or similar quality management system Experience of continuous improvement methodologies To apply for this role or to be considered for further roles, please click "Apply Now" or contact Sarah 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 »

and the client are consistently met and compliant with the specification Encourage continuous improvements across the project Promotion and implementation of the Project Quality Management System and Joint venture process Interact with project construction and suppliers in accordance with ITPs to ensure correct fabrication & installation Conversant with nuclear fabrication specifications more »

a wide range of dosimetry and engineering support equipment. Varian's Aria ver 17 patient management system integrates the service with the accredited quality management system supported on "Q-Pulse". The service has a well-established VMAT/IMRT and SABR workload with the SABR service implementing or supporting 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 »

throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our quality management system ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its more »

policies, processes, systems and procedures. Define the approach for the management of safety and compliance through the definition of arrangements within the Company Quality Management System Act as a customer-focused individual. Network across the Company to collaborate, leverage broader capability and the sharing of best practice Develop and support 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 »

various Radiotherapy Planning software tools for 3D and IMRT work. * Competency in the use of the QPulse ISO management system to update Oncology Quality Management System procedures, protocols and other documentation. Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and more »

co-workers, customers, and the community. Support quality and compliance by adhering to all procedures, work instructions, and forms per the Quality Management Systems (QMS). Completes all required training. Flexible, courteous, friendly and positive approach to work Other duties as assigned Required Skills & Abilities : Ability to train/coach more »

as and when the business requires. Ability to keep and maintain organised, accurate and meticulous records, including: - Inspection reports Rejection reports Calibration records Quality Management System documents Log and prepare test results. Work time recording. Key Skills/Qualifications: Previous experience as an Inspection/Test Engineer or practical experience 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 »

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 »

of the relevant regulations • Provide reports to management to enable them to monitor system performance. • Review and authorise documentation and processes in the Quality Management System to ensure compliance with established quality procedures and applicable regulations and alignment with other related documentation. • Identify and collaborate in the implementation of changes more »

to join the team In Milton Keynes. As the Head of Quality, you will take a lead role in managing the company's Quality management system to ensure that customers receive product to the highest standard of quality possible. The Head of Quality job based in Milton Keynes responsibilities will 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 »

to provide specialist guidance and support to the Quality Function whilst ensuring that the Business Unit remains compliant to the local Quality, maintaining Quality Management System, being a Subject-Matter Expert in specialist areas, leading to improvement initiatives to drive Quality performance. What you'll need to succeed To be 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 »

on the 1st June. Your responsibilities: Accurate and diligent in all tasks Takes the necessary actions to complete assigned tasks and evaluates processes against QMS requirements Review current processes and procedures, pro-actively highlighting areas where they require improvements or updates Supporting Quality Technologist (Labs) in their absence. This will more »

and any previous experience supporting in delivery of new product projects is highly desirable. Duties & Responsibilities: Oversee the day to day aspects of the QMS and requirements Oversee and support the wider quality team below them in the departmental structure Drive improvements/resolve issues highlighted by all audits/ more »

issues promptly and complete Export Health Certificates as needed. Quality Management Systems: Keep customer online systems updated, conduct GAP analysis, and ensure compliance with QMS, aiming for no customer non-conformances. If you're ready to take on this challenging yet rewarding role in a dynamic environment committed to excellence more »

Creates high performance by role modelling commitment to Operational Performance Management Systems principles Accountable for implementation and overall governance of end to end Quality Management System Looks and encourages others to find and reduce waste, in all its forms, in everything that we do Encourages others to seek out improvements more »

clinical study and FDA approval. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Contribute to the development of Work Instructions and Standard Operating Procedures (SOPs). Collaborate with the Engineering, Manufacturing and Biology teams working more »