101 to 125 of 266 QMS Jobs

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 »

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 »

/7 teams and help improve customer relations Contribute to the continuous improvement of the department, meeting the requirements set out in the quality management system Help maintain good customer relations and customer satisfaction on a daily basis Ensure information is shared between maintenance agents and provide reports to the more »

implementing our Food Safety. Quality and Hygiene systems in line with business growth and development. The role will be responsible for ensuring the company QMS is maintained and up to date. Ensuring compliance with BRC and Customer technical standards/codes of practice. Key responsibilities : Goods in checks. Paperwork checking more »

design requirements Support with hydraulic system expertise to the rest of the business (Production, Technical, Service, Sales and Parts) Comply with compliance with Quality Management system and health and safety legislation We are looking for someone who is/has: NVQ Level 3/HNC level education in an engineering more »

key internal departments, i.e Pre-Sales, Purchasing, Marketing and Support Services Always adhere to company policy and work in line with the Company Quality Management System (ISO 9001 and 27001 standards) To be considered for this IT Solutions Sales Specialist vacancy the ideal talent will hold: Previous IT Sales exposure more »

key internal departments, i.e Pre-Sales, Purchasing, Marketing and Support Services Always adhere to company policy and work in line with the Company Quality Management System (ISO 9001 and 27001 standards) To be considered for this IT Business Development Manager vacancy the ideal talent will hold: Previous IT Sales exposure more »

with the existing software development team. Follow all relevant medical device directives and EU GMP Annex 11 with regards to software. Keep relevant Quality Management System documentation up to date. Qualifications & Experience: 2+ years of experience creating software for a regulated field such as medical devices. 2+ years of experience more »

. Participate in NPD and Engineering Change Order processes and process compliance to product approvals Support activities related to maintaining the factorys Ex Quality Management System and internal and external factory audits. Support/coordinate with manufacturing activities to ensure product approval compliance Handle relationship with the Product Environmental Compliance more »

the team and with external partners. Adhere 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 Good understanding of communications, wiring systems and schematics or equivalent Experience with inspection and testing– C more »

ready to step up into a Principal role or an established PA looking for a change in their career. The Role: Adherence to the QMS including root cause analysis and communicating with clients on technical matters. Assistance in maintenance programs for the Departments specific analytical instrumentation and any other analytical more »

Quality Assurance Engineer with proven experience in the Aerospace/Manufacturing sector, strong understanding of Quality Management Systems (QMS) and excellent knowledge ISO 9001 & AS 9100 (desirable) is required for a permanent position for a global company in the Oldham/Ashton-under-Lyne area . Competitive salary (DoE) plus … 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 in line with customer requirements such as MSA, FMEA, CPK. … colleagues and parent company. Key Words : Quality Assurance Engineer, Quality Engineer, Quality Co-ordinator, Quality Technician, Quality Assurance, Quality Inspection, QA, QC, QMS, Quality Management System, ISO9100, AS9100, ERP, Navison, Data Analysis, Manufacturing, Production, Advanced Composite Materials, Aerospace, Automotive, Lean Manufacturing, Oldham, Ashton-under-Lyne, Manchester, Bolton, Bury, Rochdale The more »

Our client is a global leader in high performance software and innovative hardware products. The QMS Manager, will play a pivotal role in ensuring the effective implementation and maintenance of the Quality Management System (QMS) across the organization. You will be responsible for overseeing all aspects of quality management, including … timely resolution of audit findings and corrective actions. 4. Establish and maintain quality policies, procedures, and documentation to support compliance with regulatory requirements. Management of QMS Processes such as NC, CAPA and Change. 5. Collaborate with cross-functional teams to integrate quality considerations into product development processes. 6. Provide training … Regulatory Affairs). · Minimum of 2 years of experience in quality management within the medical device industry. Experience with implementing and maintaining Quality Management Systems (QMS) in accordance with ISO standards. · Knowledge of ISO Standards including ISO 13485, ISO 9001, ISO 14971, IEC 62304 and EN 60601. · Knowledge of global more »

currently recruiting for a Quality Lead to join their team. The Quality Lead will need to be experienced in developing a Quality Management System (QMS) (ISO 9001) and an Environmental Management System (EMS) (ISO 14001) as well as experience in obtaining ISO 9001 and ISO 14001 certification. This role will more »

join the company. Permanent role with a competitive starting salary and extensive benefits package. Job Overview: Maintenance and improvement of the Quality Management System (QMS). Assure the compliance of all activities with Good Distribution Practice (GDP) and Good Manufacturing practice (GMP) requirements. Responding to medical information enquiries from healthcare more »

missions. The successful applicant will become part of a world class team that is a recognized leader in maritime systems development. Primary Responsibilities Site QMS Leadership Ensure site continual compliance to the ISO 9001:2015 standard for all aspects of the QMS. Create/maintain a culture of continuous improvement. … team of quality engineers supporting the Lynnwood & Poulsbo sites. Collect and report key process indicator measurements to evaluate and improve the quality management system (QMS) Plan, coordinate and support ISO 9001 external assessments. Actively oversee the implementation of Mission Assurance goals and objectives and support Quality Engineering & Control business rhythms. … support the execution of internal quality audits for the Lynnwood & Poulsbo sites. Provide and track training of site staff to ensure awareness of quality management system processes. Project and Program support Support performance of quality inspections and verification testing of project deliverables. Conduct timely program quality audits in accordance with more »

Manufacturing support to the production areas with reference to quality issues Ensuring procedures are implemented or updated where appropriate. Actively support the business with QMS to ISO 9001:2015 certification Key skills and experience for the Quality Engineer job are: Previous work experience as a Quality Engineer or similar role more »

5y, fish bones, 8D, AQPQ, PPAP, Root Cause etc. Identifying areas to improve Quality Managing non conformances, dealing with returns Maintenance and upkeep of QMS If you are an experiencedor an up-and-comingQualityEngineerwith an engineering/manufacturing environment and seeking a challenging, exciting and varied opportunity for a leader more »

conformances and collaborate on CAPA objectives. Working with the Leadership Teams as well as building positive and effective relationships with other internal stakeholders on QMS related activities. Ready to apply? This is what you will need to demonstrate; Qualified/Certified Auditor for ISO 13485 (please note, this is a more »

for a perm role on behalf of our client based in Stanford le Hope. Duties and Responsibilities: Maintain the company's Environmental and Quality Management System frame work and ensure ongoing compliance with accredited ISO90001, ISO14001 and any other ISO standards as applicable. Manage day to day operation of the more »

testing Strong Excel knowledge and skills Excellent attention to detail - quality controlling Experience within BRC - Supply chain assurance Must have experience in running a QMS more »

with existing and new requirements. Specify audit scopes to ensure compliance with legislation, industry standards, and company policies. Maintain and enhance the ISO9001 Quality Management System and ISO14001 Environmental Management System. Approve engineering change documents and concessions, and monitor safety performance of fleet personnel and contractors. Ensure depot staff are more »

Registration (standardization) and customer specific designs. Preparation of technical & test specifications, test reports, IEC61850 files and design drawings etc. To ensure compliance with Quality Management System, Safety Procedures and Accountancy Policies. Help to maintain customer spares and customer standby systems. Preparation of method statements, risk assessments for onsite work activities. more »

training to senior stakeholders and other team members will be essential for buy-in and comprehension. You will also be responsible for the Quality Management System, portfolio product specifications and change orders. Other duties include: liaise with regulatory/PVG/medical to ensure materials development and approval in line more »