176 to 200 of 226 QMS Jobs in England

Position : Production Engineer Sector : Manufacturing/Engineering Location : Sheffield Salary : £43,000 Shifts : Days/Early finish on Friday The Production Engineer will be responsible for providing front line support for all manufacturing processes. This will be inclusive of CNC more »

Position : Production Engineer Sector : Manufacturing/Engineering Location : Sheffield Salary : £43,000 Shifts : Days/Early finish on Friday The Production Engineer will be responsible for providing front line support for all manufacturing processes. This will be inclusive of CNC more »

Job title: Laboratory Technician Reports to : Validation Team Leader Location : Manchester Science Park Contract Type : Temporary/Full-Time - 12-months fixed term contract (maternity cover) Salary & Benefits : Competitive Salary + Benefits Package About Yourgene Health: Yourgene Health is a more »

Are you a Test & Commissioning Engineer looking for a new challenge? Do you have a background in manufacturing and production? We are looking for a Test & Commissioning Engineer to join our growing CMS2 team in Portsmouth. This is a fantastic more »

with their customers, often meeting together to discuss quality matters, always putting great emphasis on processes and procedures to uphold the well established quality management system which is in place. Jobs dont come up here very often. People are happy, pay is good, the management team are encouraging, the quality … of the Quality Manager, your duties asthe company's new Quality Engineer will include: Carrying out duties relating to the upkeep of the Quality Management System Writing new procedures and updating current operating procedures as and when needed Carrying out internal quality audits according to industry standards (training courses can … confidence. You can be assured that any contact you make will be completely confidential. Key words for search purposes:Quality Engineer Quality Management System QMS more »

of audit reports for both internal and external auditors. Collaborate with the Head of GQA and the audit team to enhance the audit quality management system, actively participating in process improvements including QMS documentation updates. Maintain current awareness of the regulatory and pharmaceutical industry environment, influencing internal Business Partners and more »

and manufacturing presence to meet the demands of current and emerging markets. Duties & responsibilities include: Support the maintenance and ongoing improvement of the Quality Management System Create and submit FAIRs Support the creation and submission of PPAP Become one of the customer direct contact to resolve quality issues. Work with … ensure vendors have the processes and systems necessary to supply products that meet company quality requirements. Perform internal audits as per internal, customer and QMs criteria's. Promote and support the drive of continuous improvement in all quality processes. I'd be keen to speak to Quality Engineer's with more »

the internal calibration schedule and implementation of best practice into the business. Involvement with Design and Process FMEAs for new products and processes. Internal QMS Audits to support the internal audit team/programme. Post audit review meetings with Process Owners and follow-up review meetings. Assisting the Quality Team … with internal and External investigations and analysis, where required. Updating QMS procedures and their controlled release into the business. Data collection and analysis to support the business on-going Continuous Improvement Activities. Assisting with the weekly reporting and analysis of production scrap with a cross functional teams. Provide coaching and more »

Implementation of solutions in conjunction with suppliers to solve field service and warranty issues. Implementation of all relevant processes and procedures within the Quality Management System Communicate with personnel at all levels, internally and externally in relation to critical quality concerns. Provide support to Production by elimination of rejects from … site audits in line with the supplier audit schedule including the managing of any corrective actions that arise through problem solving exercises. Undertake internal QMS audits and process audits at suppliers. Supervision of quality personnel with regards to the resolution of internal/external material quality concerns, problem resolution Establish more »

below opportunity to join our innovative and conscientious team: Quality Systems Engineer Overall purpose of the role Responsible for driving the Quality Management System (QMS), aligning procedures and processes with rest of operations team to support the QMS. Lead and undertake … audits across all areas of the business. Provide training and champion the Quality Management System. Key responsibilities Support the effective implementation of the Quality Management System throughout the site, including any business accreditations. Maintain (and develop) the Quality Manuals and Quality Procedures and ensure contents are appropriate for business. Support … process and prevent occurrence of any non-conformity relating to product, process or system. Support develop and roll-out of activities that support the QMS and quality improvements, i.e. first off sample approvals. Support and lead process improvement activities. Write reports and present progress to Senior Management. Skills & Attributes Lead more »

MEICA Project Manager We currently have a fantastic opportunity for an experienced MEICA Project Manager to join a career enhancing project in the West Midlands. Our client is working closely with Severn Trent Water on their Capital Delivery Framework, as more »

Cranleigh STEM is working with a medical device and diagnostics manufacturer with a global reach. We are looking for a driven production manager to join our client’s team at their site in Berkshire. As a production manager, you will more »

Environmental, Social and Governance Consultant Location : Remote, requirement to travel to site assessments Salary : Competitive, DOE + Car Allowance Contract : Full time, Permanent Benefits : 25 days annual leave, buy and sell holiday scheme, employee referral scheme, private health insurance, pension more »

Environmental, Social and Governance Consultant Location : Remote, requirement to travel to site assessments Salary : Competitive, DOE + Car Allowance Contract : Full time, Permanent Benefits : 25 days annual leave, buy and sell holiday scheme, employee referral scheme, private health insurance, pension more »

Job summary INTERNAL ONLY TO NORTH CUMBRIA INTEGRATED CARE NHS FOUNDATION TRUST (NCIC) EMPLOYEES ONLY Specialist Biomedical Scientist, Immunology/Virology Band 6, 75.00 hours per week. *Applications are only invited from current band 5 Biomedical Scientists in Virology/ more »

Principal Electrical Design Engineer Minimum of 10 years of relevant electrical design experience Whippendell Marine is a long-established supplier of LV electrical engineering solutions for the naval environment. We specialise in the design, manufacture and support of motor starters more »

Quality Management System Lead Permanent Reading (2-3 days/week in office) MBNL is owned equally by EE and Three, two of the UK's most recognisable and innovative mobile operators. They are our shareholders, but to us they are also our customers. Continuing to manage, maintain and enhance … 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 »

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 »

problems/trouble shooting through data analysis and evaluation, and develop lab technicians to have the same approach. Demonstrates sufficient knowledge in the laboratory QMS and plays an active part in building and maintaining the QMS and laboratory accreditation. Displays drive and motivation to continually improve quality based performance. Internal more »

their motivated technical services team, this is a great opportunity to become part of the Bakkavor Group. Responsibilities include: - Managing and developing the Quality Management System across the entire business ensuring that all QMS documentation is up to date, relevant & controlled and meets the requirements of legislation, industry standards, Bakkavor … to the Technical & Operational teams thus driving continuous improvement and best practice across site. - Establishing and maintaining a process of horizontal auditing against the QMS to ensure compliance. To establish or review and amend procedures as required by new customer codes of practice, new business initiatives or new internal systems. more »

a medical manufacturer, offering progression, additional training, healthcare benefits, and more. THE ROLE: * Quality document Controller * Assist Quality Manager * Ensure Guidelines are followed * Maintain QMS * Mon-Fri 9am-5pm THE PERSON: * Document Controller with Quality background * Knowledge of ALCOA * Audit skills * Commutable to Worcester Reference Number: BBBH13645 Key Words: Medical … ALCOA, Devise, Quality, Assurance, QMS, Management, Audit, Document Controller, Worcester, Droitwich Spa, Bromsgrove, Stourport-on-Severn, Kidderminster, Great Malvern If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV. We are an equal opportunities employer and welcome applications from all 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 »

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 »

Workshop Campaign Vehicle Quality Coordinator Location : Volkswagen Group's National Learning Centre, Wymbush Salary : Competitive, DOE + Benefits! Contract : Permanent, Full time Benefits: 25 days plus annual leave plus BH, Holiday buy and sell scheme, Employee referral scheme, Private health more »

Automotive Repair Quality Specialist Location : Volkswagen Group's National Learning Centre, Wymbush Salary : Competitive, DOE Contract : Permanent, Full time Benefits: 25 days plus annual leave plus BH, Holiday buy and sell scheme, Employee referral scheme, Private health insurance, Pension contribution more »