1 to 25 of 59 Permanent QMS Jobs in the South East

and working with suppliers to arrange processing and shipment of critical devices. There will be some involvement with supporting other areas of the Quality management System as outlined in the Key responsibilities below. Key Responsibilities Ensure compliance with ISO 9001 Quality, ISO 14001 Environmental, and ISO 45001 Health and Safety more »

or a related field. - Proven experience in a Quality Systems role within the electronics industry. - Strong knowledge of ISO 9001 and experience with quality management system audits. - Excellent analytical skills and a methodical approach to problem-solving. - Effective communication skills, with the ability to engage stakeholders at all levels. Apply more »

Overview: Support the quality team with co-ordinating and conducting internal audits in accordance with the internal audit plan, assist with maintaining the quality management system across all departments. Identifying areas for improvement of internal processes to meet and exceed industry standards and customer expectations. Key Responsibilities: Perform audits of more »

SQL and either Python or R. Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System (compliant with ISO 9001 and 14001). PERSON SPECIFICATION Required skills and experience Significant experience of working in the data domain in technical roles more »

with the Purchasing team and suppliers in order to support component issue resolution. Support with the administration and maintenance of the Quality Management System (QMS). Gather data and generate reports to support decision making within the team and wider business. Support the Quality Manager to ensure the ongoing compliance … environment. Auditing: Experience in conducting audits against ISO9001, processing audit documentation and improvement reports. Experience in administration and maintenance of the Quality Management System (QMS) Compliance: Acts with integrity and can work in accordance with regulation and compliance. Data Visualisation Software: Familiar with data visualisation software, such as Power BI more »

OX29, Witney, Oxford. £45,000 - £50,000 Quality Engineer, Quality Systems Management, Quality professional based near to Eynsham, Witney, Oxford. ISO 9001, AS9100, TS16949, QMS, Auditing, Quality compliance within a manufacturing environment (Any exposure to PPAP, APQP, FMEA). Working for a medium sized business that manufactures parts for highly more »

Our client is currently recruiting a Technical Engineer who will ensure that projects are managed in accordance with our client's Quality Management System, Group Policies and industry standards. Responsibilities To support the Technical Manager and Senior PM in the delivery of the Operations, Special Projects and Marine Construction Projects. more »

Main Duties (but not limited to): Completing technical checks in the factory (quality checks, carcase inspections, pH testing, steriliser checks etc) Reviewing and filing QMS paperwork from various production departments. Liasing with production teams in relation to paperwork completion, where necessary. Collating and registering all samples and results for microbiological more »

team. Internally will liaise with Team Leaders & Quality Manager. QUALIFICATIONS and PERSONAL PROFILE Must have Industry Standard Inspection Qualifications (IPC). Awareness & understanding of QMS Disciplines IAW BS EN ISO 9001:2008 & AS EN 9100. Awareness & understanding of ESD Controls. Reading & understanding Complex Engineering Drawings & Instructions. Key personal skills:- Excellent more »

required in Quality Engineering in a manufacturing environment Role: Reporting to the Senior Quality Lead, you will be responsible for all aspects of Quality, QMS, Continuous Improvement and Business operating systems and play a key role in the day-to-day quality operations at our UK factory in Slough. The more »

and effluent batches. Monitoring trends in data and reporting any issues directly to Quality Management. Assist Quality Manager in the maintenance of the Quality Management System as required. Reporting and managing of data on trends or certain batches declining if applicable, product quality and comms. Writing SOP and risk assessments. more »

years in a GMP environment Basic experience in pharmaceutical manufacturing, distribution, and control measures Basic experience in Quality administered systems. Previous use of TrackWise® QMS beneficial. Experience in operating in a QMS. Experience in writing deviations, change controls, CAPAs, complaints. Experience in supporting internal and external audits including BOH inspections. more »

in the South East market. We are seeking a dynamic and experienced Technical Sales Manager to support our sales efforts and oversee our quality management system, and maintain testing procedures to ensure excellence in our product offerings. Responsibilities: 1. Sales Strategy Implementation: Execute a sales strategy tailored to the South more »

to detail and quality. • Problem Solving • Customer Focus • Functional/Technical Skills • Process Management • Understanding of program management, operations, distribution, delivery performance and quality management system • Understanding of root cause analysis, lean tools, procurement and supply chain management. • Familiarity with Sarbanes Oxley. • Exportation to international customers more »

collect information for the client handover pack 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 network commissioning experience on renewables and utility scale projects engineers in electrical substation environments of undertaking more »

the business. The Assurance Analyst will be responsible for the successful management and improvements of the Corporate Risk Register (RAID), the management of the QMS (ISO9001) and supporting the PMO. The Assurance Analyst will also be required to develop effective relationships with stakeholders across the business to deliver on objectives. … owners accountable for: Certifications Updating Partner Portal Ensuring objectives are being met in agreed timeframes QMS Management and continual improvement of the QMS (Quality Management System) Raise awareness of the QMS to the business and provide regular training and updates using corporate communication channels Hold Process owners to account for more »

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 »

or above Up to date & in-depth knowledge of quality and sub-specialist area within primary discipline. Desirable Evidence of understanding quality and the QMS within Pathology and being able to analyse and interpret quality data. Evidence of being able to perform audits. Equality, Diversity & Inclusion Essential Evidence of having more »

the regulatory requirements of Annex 1 EU GMP. Lead Responsibility for the maintenance of all aspects of the aseptic units reactive and proactive quality management system Lead Responsibility for the release of aseptically prepared products, the department has an annual workload of up to 50,000 items. Lead Responsibility for more »

Significant leadership experience in QA. Expertise in regulations and GMP. Strong managerial and problem-solving skills. QP qualification and relevant degree. Familiarity with electronic QMS systems. more »

define process parameter to ensure process capability 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 to find out more, along with your availability and more »

define process parameter to ensure process capability 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 to find out more, along with your availability and more »

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 »

from personal or Sonardyne work activities. To ensure awareness, understanding and adherence to all Sonardyne Policies and Procedures including Health & Safety, Anti Bribery, ISO9001-QMS and Operational requirements at all times. To take an active part in the Sonardyne Continuous Improvement Process, through providing suggestions for corrective actions, suggestions, initiatives 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 »