1 to 25 of 38 QMS Jobs in the North of England

for improvement. Collaborate with manufacturing engineers on customer requirements to ensure compliance within the Production environment. Assist in general Upkeep & continual improvement of the QMS to ensure compliance to EN9100. Develop inspection and risk management methods to analyse product quality inline with customer requirements such as MSA, FMEA, CPK. Perform more »

programme Maintain network of external audit providers to support CMC, pre-clinical and clinical activities. Support the management, implementation, and maintenance of the Quality Management System to support clinical development activities. Support senior management in providing direction and leadership to staff to ensure a quality mindset is embedded in the more »

background in manufacturing, apply now for an immediate response! The Job Youll Do; To lead the ability to maintain ISO accreditation and improve quality management system To lead and assist in reducing supplier quality problems (MRB) To lead and assist with shop floor quality problems and reduce number of NCs 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 »

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 »

with Technical, Quality and Operations Teams to ensure product development SOPs are published, maintained and updated - Ensure processes and outputs integrate successfully with Quality Management System and processes - Maintain a register of existing, proposed and potential IP for new product development - Acquire, maintain and apply expertise in areas of regulatory 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 »

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 »

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 »

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 »

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 »

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 »

bar to make up our datalogger tools. This process requires great attention to detail due to the fine tolerances involved. • Work to all Company QMS policies and procedures as per ISO 9001:2015. • Ensure that a safe working environment is maintained at all times through compliance with Health and safety more »

and Qualifications: Demonstrated experience in the design and development of products - Medical industry advantageous Design or Engineering Degree preferred Familiarity with regulatory standards and QMS - ISO13485 advantageous CAD proficient, preferably Solidworks Plastic manufacturing process knowledge If you want to be part of a team dedicated to making a meaningful impact more »

formal qualification in quality, although this isnt essential. About the Job Youll take the responsibility of ensuring products are manufactured meet the customer specifications. QMS maintenance that complies with ISO9001. Youll lead a small team, youll be able to influence and motivate to ensure goals are met. Youll ensure internal more »

in upholding the highest standards of quality! For this role,you must be willing to obtain CTC clearance Key Duties • Active promotion of Quality Management system awareness. • Review and update site quality plan • Produce and review Inspection and Test Plans and monitor compliance • Production of Work Packs • Weld Inspection (only more »

skills, special stains techniques and Immunohistochemistry Good understanding of Health and Safety requirements within the scope of practice Desirable Knowledge of using a Quality Management system Training and Experience Essential Competence in a wide range of complex laboratory procedures Experience in the day to day guidance and support of junior 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 »

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 »

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 »

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 »

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 »

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 »