1 to 25 of 37 Permanent ISO 9001 Jobs in the East of England

8D problem solving methodology. You will also play a key role in the internal auditing process, ensuring the business stays on-track for its ISO 9001 certification. The technology under development represents a close coupling of mechanical, electrical, control, and software systems and alterations to any one area … and electro-mechanical hardware testing. Requirements: Commercial experience as a quality engineer or similar at a high-volume electronics manufacturing company Strong familiarity with ISO 9001 Good degree (1st or 2:1) in an engineering discipline Full and unrestricted rights to work in the UK Based in Cambridge … expand and strengthen their skills, learning from expert colleagues from a variety of technical backgrounds. An excellent salary is on offer. Keywords: Quality, QMS, ISO, ISO:9001, 8D, PDCA, Continuous Improvement, Lead Auditor Another top job from ECM, the high-tech recruitment experts. Even if this job more »

passionate thinkers, makers and doers working across a range of disciplines including UX, strategy, design, development, hosting, project management and support. We’re ISO 27001, ISO 22301, ISO 9001, and Cyber Essentials Plus certified – as well as a certified Great Place to Work. We also hold … ISO 14001 & Green Mark certifications, and our commitment to environment sustainability sits at the heart of Zoocha’s products and business processes. We build long-lasting relationships with clients and push them, ourselves and the world around us forward through the creation of beautiful, accessible and useful digital products more »

/Medical Device Quality Assurance department. - Knowledge of GxP and Quality related regulations and standards within the Pharmaceutical/Medical Device industry. - Familiarity with ISO 9001, ISO 13485, GCP is essential. - Knowledge of ISO 21CFR Part 820, ISO17025, Clinical Trials experience, ISO13485 Lead auditor would be more »

passionate thinkers, makers and doers working across a range of disciplines including UX, strategy, design, development, hosting, project management and support. We’re ISO 27001, ISO 22301, ISO 9001, and Cyber Essentials Plus certified – as well as a certified Great Place to Work. We also hold … ISO 14001 & Green Mark certifications, and our commitment to environment sustainability sits at the heart of Zoocha’s products and business processes. We build long-lasting relationships with clients and push them, ourselves and the industry around us forward through the creation of secure, performant, reliable and useful digital … a project Staying abreast of the latest goings on in the Linux, security and DevOps fields Creating and maintaining documentation that contributes to our ISO certifications In-future, potentially participate in on-call rotation Proactive maintenance across systems Investigate problem tickets Handle escalated issues that require sysadmin or DevOps more »

Quality Management System processes are established, implemented and maintained. Key Accountabilities Implement and maintain the companys quality management system (QMS) to ensure compliance with ISO 9001 and other relevant standards. Perform regular audits of processes, products and services to identify areas of improvement and ensure adherence to quality … of improvement, supporting the team to overcome any obstacles. The Candidate Previous experience within a compliance or quality assurance role. Experience and understanding of ISO 9001 Background and experience of top down Quality Management Positive can-do personality with a willingness to learn and develop their skills The more »

delivered. Interpreting technical drawings for planning, executing, and specifying material to support job duties. Provide support to technicians carrying out Instrumentation Loop testing to ISO 9001 & ISO 14001 standards when required (assistance from a Software perspective only) Taking ownership of own training and development plans. Responsible for more »

our team and any contractors or visitors. Adheres to, improves and exceeds requirements of all current and future accreditations that we hold such as ISO 9001:2015, ISO 14001:2015, BRCGS, SEDEX, FSC, Eco Vadis etc. Regular Health & Safety reviews and process updates. In line with legislation more »

/fit-out and testing of SEA-KIT s USVs to improve the quality of the vessel design and build. Lead the company s ISO 9001 annual recertification, and oversee external reviews and audits to maintain certification. Lead the implementation of required management systems and processes required for … additional ISO certifications. SEA-KIT s head office and manufacturing yard is based in Tollesbury, Essex. The role involves some travel within the UK and potentially to international locations. Responsibilities Generate and cultivate a strong culture of HSE awareness. Management, implementation, maintenance and continuous improvement of the company s … with relevant QHSSE experience in a manufacturing and/or project environment. Experience in the implementation and maintenance of a Quality Management System/ISO certification is essential. You are well organised, with good analytical and critical thinking skills, and excellent verbal and written communication skills. You are flexible more »

for new customers or initiatives and manage the projects to deliver them to operational BAU Decision Making Guidelines and processes: • Noatum Policies and Procedures. • ISO standards as determined by the business for example, ISO 9001 Quality/14001 Environment/18001 OHSAS • Health and Safety guidelines • Stock more »

HNC Engineering desirable. NVQ Qualification in Nuclear/Engineering related area. Demonstrable experience in a Quality Engineering (QA/QC) related position. IRCA approved ISO 9001:2015 Lead Auditor qualification. Skilled and experienced Auditor. Working knowledge of Microsoft Programs and Business Process Mapping. Ability to effectively lead a more »

Engineering & Design team. To participate actively in Continuous Improvement, Lean initiatives and other activities to improve the overall efficiency of the Company, including via ISO 9001 accreditation. To ensure that duties are carried out in accordance with all Company policies, procedures and processes. To carry out any other more »

and reporting across all stakeholders Project requirements management Performance management and personal development reviews Reinforcing process and contributing to continual process improvement Ensure that ISO9001 and ISO14001 procedures are adhered to at all times Essential skills: Line Management: A good appreciation and preferably experience incorporating: Management of a multidisciplined team more »

external QHSE audits, along with a strong grasp of engineering drawings and manufacturing methods. Required qualifications for this role include recognised Engineering certifications and ISO9001, ISO14001, and ISO45001 Certified Auditor qualifications. Additionally, proficiency in MS Word and Excel would be highly valued. This is a permanent, full-time role Monday more »

well as performance management and personal development reviews. We need you to reinforce the process and contribute to continual process improvements and adhere to ISO9001 and ISO14001. This role is a full-time position, 40 hours a week based in our St Neots office! We do offer hybrid working more »

in the CAE family, because of our unique understanding, total commitment and positive engagement. We get recognised in a number of different ways: Having ISO9001 and 27001 certifications With multiple awards from manufacturers including Cisco and Dell Technologies Being 3 star accredited with the Service Desk Institute Within our industry more »

scalable, allowing personalised therapies to be affordable for more people. To commercialise their technologies, they are recruiting a Quality Manager to lead them through ISO 9001 and other regulations. This would include developing and building quality frameworks for all stages of project development and manufacture through the management … in from all stakeholders. Requirements: Graduated with a bachelor's or master's in engineering or similar. Substantial demonstrable experience leading a company through ISO9001/13485 relating to medical device instrumentation development and manufacture. Further exposure to GMP manufacture for biological products would be desirable. Comprehensive experience with "quality … considered. On offer is a healthy benefits package including private medical insurance (including immediate family dependents), enhanced company pension contributions and annual bonus. Keywords: ISO9001/13485, Quality Management, Auditing, Medical Devices, Regulations, Development, Manufacture, Cambs/Herts Border Another top job from ECM, the high-tech recruitment experts. Even more »

Essentials: - - Degree level or above in electronics or similar discipline. - Significant experience of working within a high-volume electronics manufacturing environment - Auditing experience to ISO 9001 standards. (Ideally a lead auditor) - working knowledge of 8D and continuous Improvement You will be working or ground breaking technology, offered a more »

/HNC level or above in electronics or similar discipline. - Significant experience of working within a high-volume electronics manufacturing environment - Auditing experience to ISO 9001 standards. (Ideally a lead auditor) - working knowledge of 8D and continuous Improvement You will be working or ground breaking technology, offered a more »

bodies such as LUV, CE, UL, IPC, or similar. Capable of leading compliance and reliability activities for assessing product compliance. Previous experience with an ISO9001, AS9100, IATF16949 or similarly regulated manufacturer. Have excellent communication skills both verbal and written. Be self-motivated and have a positive attitude Good problem-solving more »

experience Strong knowledge and understanding of SMT production lines Experience applying Continuous Improvement methodology, Six Sigma, and tools for data driven decisions Familiarity with ISO9001 principles Auditor experience Strong analytical and problem solving abilities (5 Whys, 8D, Kaizen) Ability to be flexible around international travel (10% travel expected) Must have more »

processes, ideally ATMP's or biologics. Sound knowledge of EMA and FDA regulatory environments and requirements. Familiar with global standards related to quality e.g. ISO 9001. Experience working as a Quality Specialist or equivalent in biologics and preferably cellular and/or gene therapies. Ability to manage multiple and more »

ability to respond to emergencies. Experience of maintenance repairs, such as electrical, and plumbing. To have an understanding of Quality Standards such as ISO13485, ISO9001, ISO14001 or other applicable standards, working with a Quality Management System. Ability to work independently and manage time effectively. Maintain accurate records of maintenance tasks more »

experience in an engineering and manufacturing environment theoretical knowledge in engineering principles. in 2D CAD software (preferably Autodesk products) and MS Office Preferred: with ISO 9001 and engineering documentation systems to subsea engineering or related industries Education Bachelor's degree in Electrical Engineering or Mechanical Engineering. Ready to more »

and can remain calm even if pressure is getting high and resistance is met by colleagues, contractors, or stakeholders Strong knowledge of Quality Standards: ISO 9001 Series Extensive knowledge and application of the Quality discipline within Projects and Operations; Renewables/Oil and Gas Sector knowledge and experience more »

multi-disciplinary engineering/utility/DNO environment Ideally Chartered Engineer or relevant experience Relevant management or professional qualifications Understanding of management systems to ISO9001, ISO14001 and OHSAS 18001 Knowledge and understanding of Industry Standards, relevant codes and Systems Knowledge of protection and control schemes on the 11kV to 132kV more »