1 to 25 of 71 Permanent QMS Jobs in the UK excluding London

. Degree in Life Science or other relevant disciplines. Knowledge of current GMP requirements within major pharmaceutical markets. Knowledge and application of the principles of the Quality Management Systems (QMS). Comfortable with verbal and written English. Preferred Qualifications & Skills: Knowledge of/experience in API, sterile, parenteral, and/or biopharmaceutical manufacturing processes/environments Auditor certification from relevant More ❯

requirements for Quality activities. Stay up to date with the latest advancements in Quality management technologies, methodologies and best practices. Qualifications & Requirements - Quality Systems Engineer Minimum 3 years Quality Management System experience in a complex ISO9001/AS9100 certified manufacturing environment. Skilled in documentation management and configuration control Proficient auditor of management systems and processes Experienced in the use of More ❯

requirements for Quality activities. Stay up to date with the latest advancements in Quality management technologies, methodologies and best practices. Qualifications & Requirements - Quality Systems Engineer Minimum 3 years Quality Management System experience in a complex ISO9001/AS9100 certified manufacturing environment. Skilled in documentation management and configuration control Proficient auditor of management systems and processes Experienced in the use of More ❯

root cause analysis investigations for internal non-conformances. Support continuous improvement teams for quality improvement and waste reduction. Support the QC manager in ensuring standards defined within the quality management system are maintained and reflect the correct standards to match customer expectation. To highlight inconsistencies and errors within QC documentation and processes Ensure these are recorded in an appropriate manner More ❯

risk issues, and support inspections. Candidate Profile Basic Qualifications & Skills Experience in regulated environments like pharmaceutical manufacturing. Degree in Life Sciences or related fields. Knowledge of GMP requirements and QMS principles. Proficiency in English. Preferred Qualifications & Skills Experience with API, sterile, parenteral, or biopharmaceutical manufacturing. Auditor certification from relevant organizations. Application Details Deadline: Sunday 31st August. Please include relevant competencies More ❯

quality system to ISO 13485 standards and associated product certification. As a Quality Systems Engineer, you will: Support the maintenance and continuous improvement of our ISO 13485 compliant Quality Management System with activities including document control, training management and change management. Draft and update procedures, work instructions, and quality documentation. Collaborate closely with Engineering (Software and Hardware) and Customer Support More ❯

for delivering high levels of GMP, food safety and integrity standards within the factory. Support in driving food safety, compliance, and quality improvements across site. Update and maintain the QMS, conduct audits and ensure any corrective actions are implemented. Support external audits (BRC, customer etc). Collaborate cross-functionally with on site and group teams. Skills Experience in a QA More ❯

progress, co-ordination and feedback Responsible for the production, review and monitoring of construction methodology documentation including RAMS and ITP's to ensuring compliance with the company's quality management system and the employers requirements. Responsible for production of as-built documentation from site. Responsible for materials forecast, procurement and reconciliation. Help collate and site data for inclusion in Daily More ❯

communication skills to team, peers, and all levels of management Desired Characteristics NPI process knowledge/experience Test Systems Sustainment process knowledge/experience Familiar with highly regulated Quality Management System(s) Good people skills and a firm interest in developing engineers. An appetite to drive Continuous Improvement initiatives and invest in process development/refinement. GE supports and encourages More ❯

Systems : To complete all admin on time and accurately and ensure that all relevant paperwork is filed and archived to support due diligence Document Control : Administration of site Quality Management System and associated control documents including relevant factory paperwork Customer Management : Administration of customer complaints including login of data, investigation of issues, trending and reporting of data Customer Management : General More ❯

for a Quality Manager to join our market leading client based in Wembley on a permanent basis. The selected Quality Manager will Implement and maintain our client's Quality Management System in accordance with BS ENISO 9001 and liaise with the Quality Management Department, internal and external customers as well as suppliers as appropriate with regard to Quality issues. As More ❯

Proven track record in a quality management role within electronics manufacturing or a similarly regulated industry Strong working knowledge of ISO standards (ISO9001, ISO13485, ISO14001, ISO45001) Proven experience in QMS development , Lean , and Continuous Improvement (CI) methodologies Familiarity with embedded systems , cables , touch screens , or electronic engineering Experience managing supplier quality , customer returns , and audit processes Ideally holds a NEBOSH More ❯

Proven track record in a quality management role within electronics manufacturing or a similarly regulated industry Strong working knowledge of ISO standards (ISO9001, ISO13485, ISO14001, ISO45001) Proven experience in QMS development , Lean , and Continuous Improvement (CI) methodologies Familiarity with embedded systems , cables , touch screens , or electronic engineering Experience managing supplier quality , customer returns , and audit processes Ideally holds a NEBOSH More ❯

Diagrams. Good fundamental electrical knowledge and ability to understand/interpret system drawings. Sound grasp of general IT/OT Technologies and development methodologies. Awareness/understanding of Quality Management System procedures. Knowledge of Windows Operating System configuration and lockdown. Knowledge of network switch and firewall configuration and network management packages. Electrical & Electronic or Electrical or Software Engineering degree (min More ❯

and adhere to relevant contract terms • Must enjoy working in a fast-paced environment with a large range of internal and external stakeholders • Adherence to the Company's Quality Management System to ensure that all work is handled Securely, Professionally and Diligently Skills, Knowledge and Experience: • Familiarity with life sciences and/or healthcare IT and software is a plus More ❯

will be working under minimal supervision follows process instructions, drawing, test and repair schedules, to assemble, test and repair product and customer returns, to the requirements of the quality management system, and to achieve company and customer requirements. Location: Christchurch UK Benefits: Paid Time Off | Retirement with Employer Match | Health and Wellness Benefits | Learning and Development Opportunities | Competitive Pay | Bonus More ❯

procedures. Maintain accurate inspection records and quality documentation . Collaborate with production, engineering, and quality teams to support continuous improvement initiatives. Participate in internal audits and contribute to maintaining QMS compliance. Skills & Experience Required: Experience in quality inspection within an electrical or electro-mechanical manufacturing environment. Strong understanding of electrical principles , wiring practices, and circuit verification. Ability to interpret and More ❯

life sciences as a consultant, business, or IT representative Direct experience with systems such as LabWare, SQL LIMS, LabVantage, StarLIMS, SampleManager, SmartLab, BIOVIA, Nugenesis, Empower, Laboratory Information Manager System, QMS, ELN, LIMS, and other informatics or similar systems Consulting experience Veeva's headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the More ❯

Failure Mode and Effects Analysis (DFMEA) process. Skilled in applying structured problem solving approaches and analytical tools such as 8D and Ishikawa. Skilled at working in a software quality management system and applying industry best practice such as MISRA C. Knowledge of ASPICE development process desirable Skilled in the application/selection of relevant engineering analytical techniques, manufacturing processes, materials More ❯

Failure Mode and Effects Analysis (DFMEA) process. Skilled in applying structured problem solving approaches and analytical tools such as 8D and Ishikawa. Skilled at working in a software quality management system and applying industry best practice such as MISRA C. Knowledge of ASPICE development process desirable Skilled in the application/selection of relevant engineering analytical techniques, manufacturing processes, materials More ❯

teams to troubleshoot field-reported product issues Test software release candidates Write test procedures and define acceptance criteria Support the development of automated system tests Contribute to the quality management system for processes and documentation Participate in continuous improvement and problem-solving activities Conduct factory acceptance tests for customer systems Occasional travel to third-party manufacturing and test sites Experiences More ❯

teams to troubleshoot field-reported product issues Test software release candidates Write test procedures and define acceptance criteria Support the development of automated system tests Contribute to the quality management system for processes and documentation Participate in continuous improvement and problem-solving activities Conduct factory acceptance tests for customer systems Occasional travel to third-party manufacturing and test sites Experiences More ❯

all functions. You will support the administrative aspect of the Technical Department taking responsibility for the day-to-day management and maintenance of some or all of the following: QMS, HACCP, Technical Reports, Non Conformance Logs, complaints, microbiological & nutritional surveillance; this work includes data entry, trending, information requests, co-ordination of actions, change management procedure and communicating to relevant parties. More ❯

all functions. You will support the administrative aspect of the Technical Department taking responsibility for the day-to-day management and maintenance of some or all of the following: QMS, HACCP, Technical Reports, Non Conformance Logs, complaints, microbiological & nutritional surveillance; this work includes data entry, trending, information requests, co-ordination of actions, change management procedure and communicating to relevant parties. More ❯

plays a crucial role in ensuring that project quality requirements and compliance standards across the organisation are met and managed effectively. Key Responsibilities: Develop, implement, and maintain a quality management system demonstrating regulatory compliance. Lead continuous improvement activities to enhance business and project processes. Conduct and manage audits on projects and processes, implementing necessary improvements. Coordinate and monitor quality policies More ❯