226 to 250 of 276 QMS Jobs

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 »

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 »

Ambitious and experienced engineer initially focused on nuclear-related applications, with specific involvement in an embedded team delivering a national project currently at concept phase. Background Wilde Analysis is a multi-disciplined consultancy and software channel partner, specializing in simulation 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 »

drive and accelerate the Company quality objectives and improve both internal and external quality. Develop, implement and maintain processes for the Quality Management System (QMS). In return my client are offering an excellent salary and benefits such as Pension scheme, Health Surveillance,Use of Company Gym and others to more »

Directive 2001/83/EC , with previous operational QP experience. Additional responsibilities will include : Acting as GMP Subject Matter Expert for QMS site compliance Maintaining QMS systems, leading by example to implement and coordinate updates accordingly. Leading and coaching QA Team Ensuring all activities are completed in line with more »

perform research and give technology recommendations that can meet or satisfy three key points: Cost Effectiveness, Productivity Increase, Efficiency · Adhering to Quality Management System (QMS) and self-enforcing of procedures and regulations. · Communicate concerns or recommendations to team lead related to current running system. · Participate and contribute in regular team more »

technical & commercial bid efforts in conjunction with the Tendering & Estimating department. " Ensures that project activities adhere to the requirements of the Quality Management System (QMS) and adhere to the requirements of the HSE management system. Role responsibilities include: " Providing leadership for the overall planning, direction, coordination, integration, execution, control and 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 »

required to meet budsheet objectives. To assist in developing test processes and procedures. Capital and tooling budget control management. Management of Quality Systems. Ensuring QMS up to date, in-line with current customer and legislative requirements. Communicating any changes to the QMS to the audit team and company in general. 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 »

or preparation of responses to deficiencies) and on-site presence as required. Develop audit systems to ensure key elements of the Dechra GxP Quality Management System and the requirements of the product licences/marketing authorisations are effectively implemented throughout the internal and external manufacturing network (as required) across the … and GMP/GDP regulatory compliance. Disseminate regulatory intelligence related to industry best practice, upcoming regulations, audit/inspection trends as well as general QMS training and product quality knowledge. Support the QMS Manager in the configuration of the eQMS supplier qualification, audit, and inspection processes within the eQMS system. 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 »

🏆Do you have some experience working with s oftware as a medical device ? 🌍My client is looking for a driven and detail oriented Quality Manager to join there team! They are looking for a highly talented The Quality Manager to more »

Quality Engineer/Quality Control Engineer/Reliability Engineer required to join a global engineering manufacturer. The successful Quality Engineer/Quality Control Engineer/Reliability Engineer will maintain quality management systems, conduct audits, manage calibration systems, and implement process more »

The role of the QA Compliance Officer is to support governance and compliance of the Pharmaceutical Quality Management System (PQS) at Piramal Grangemouth and maintenance of Regulatory Registrations/Licenses/Certifications. The role will support the site and related functions in maintaining compliance with GxP regulations and applicable quality … key quality system elements and compliance improvements, working closely with relevant stakeholders on site. Role •Supporting key quality system elements, including activities relating to QMS monitoring, Qualification of Vendors, Audits (Self-Inspections, Vendor Audits, Customer Audits). •Support updates to regulatory agency registrations as applicable. •Support tracking of site compliance … quality improvements •Support and track regulatory findings and trends that may lead into a focus of regulatory inspections •Support review of procedures and other QMS related documentation according to internal guidelines and UK/EU/US/ICH and other region specific guidance. •Lead Quality Management Review meetings highlighting more »

The role of the QA Compliance Officer is to support governance and compliance of the Pharmaceutical Quality Management System (PQS) at Piramal Grangemouth and maintenance of Regulatory Registrations/Licenses/Certifications. The role will support the site and related functions in maintaining compliance with GxP regulations and applicable quality … key quality system elements and compliance improvements, working closely with relevant stakeholders on site. Role Supporting key quality system elements, including activities relating to QMS monitoring, Qualification of Vendors, Audits (Self-Inspections, Vendor Audits, Customer Audits). Support updates to regulatory agency registrations as applicable. Support tracking of site compliance … quality improvements Support and track regulatory findings and trends that may lead into a focus of regulatory inspections Support review of procedures and other QMS related documentation according to internal guidelines and UK/EU/US/ICH and other region specific guidance. Lead Quality Management Review meetings highlighting more »

conformance. Service Hub administration and communication of areas requiring action to ensure continuous compliance. Provide a launch, withdrawal, and management service for all Quality Management System documentation. Challenge and drive quality and audit ready culture across the business. Ensure systems are in place to capture site specific QMS documentation and more »

required corrective actions Ensure products and ingredients are evaluated against specification Support the promotion of a quality culture and help to develop the quality management system Coordinate QA requirements for product launches e.g. update of required documentation/systems, liaison with Process team/line support to ensure product is … manufactured to correct standard Plan and co-ordinate work of the QA team to meet requirements of the quality management system and the needs of the business About you. Ideally you will have a good practical working knowledge of food safety legislation and quality requirements. A strong QA background is 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 »

Expleo is a trusted partner for end-to-end, integrated engineering, quality services and management consulting for digital transformation. We help businesses harness unrelenting technological change to successfully deliver innovations that will help them gain a competitive advantage and improve 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 »

Job summary An opportunity has arisen for an experienced HCPC-registered Biomedical Scientist to join the Pathology Team at Ramsay Rivers (Harlow/Sawbridgeworth). This is a strategically located laboratory within the Ramsay Healthcare Group of hospitals. The laboratory more »

Quality Administrator QMS jobs role ; quality administrator, QMS Coordinator jobs aerospace, automotive, motorsport Business works with international aerospace, defence, motorsport and space customers globally Backed by a multinational PLC ; share price is up over 95% in the past 3 years QMS jobs role/Quality Administrator jobs would suit an … ambitious QMS Coordinator/ISO Coordinator who wants to take ownership for an evolving QMS. £30,000 - £35,000 TBC still being defined. Are you a Quality Administrator, Quality Coordinator, ISO Coordinator, Quality Systems Manager, Quality Auditor or similar (someone working with the QMS) seeking quality jobs? Are you seeking … quality jobs, QMS jobs or quality assurance jobs? Are you seeking quality jobs in Royal Wootton Bassett , Swindon, Chippenham, Cirencester, Wiltshire region? Backed by a multinational PLC ; share price is up 95% in the past 3 years They work with international aerospace, defence, motorsport and space customers globally Friendly company 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 »