1 to 25 of 33 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 »

oversight of GMP and compliance within company operations, providing guidance on GMP, GDP and GLP ensuring compliance with internal and external requirements with both ISO 13485 and ISO 9001 standards. Requirements for this role: Degree in relevant biological discipline Significant experience within industry in similar role, within … ISO 13485 and ISO 9001 environments Experience with internal auditing Experience in manufacturing equipment validation Interviews are imminent so please apply now or contact Chris Morris at Science Solutions for more information. more »

be responsible for ensuring that the systems and processes in place for current Good Distribution Practice, MHRA guidelines, Home Office controlled drugs license and ISO-9001: 2015 and ISO 13485 standards are adhered to and that the procedures and appropriate training for the team and wider DD Group … Distribution Authorisation, GDP Guidelines 2013/C 343/01, Human Medicines Regulations 2021 relevant MHRA Guidelines, legal requirements, and updates Ensure compliance with ISO 9001: 2015 and ISO 13485: 2016 standards. Ensure the QMS is implemented and maintained. The RP must approve, sign and date, all … associated standards Good working knowledge of product classification for medical devices, specifically selecting appropriate classification, and conformity assessment route. Formal Training in ISO13485/ISO9001 auditing (preferable) Understanding of foreign regulatory requirements, and introduction of new products to new markets would be advantageous. What we offer Annual bonus, based on 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 »

refrigeration specifications are feasible to source by connecting to suppliers and manufacturing operations Provide specific documentation related to product design to meet regulatory compliance: ISO 9001, 13485 and organization requirements Assist on quality complains from the field by providing technical support to identify root cause, short- and long … and heat transfer Design Engineer will have experience working in formalized phase-gate product development process, using Design tools such as DFM, FMEA and ISO 9001 design controls Experience on SolidWorks (CAD) If you would like to find out more about this Design Engineer opportunity, click the "APPLY more »

wide range of social events on offer across our three offices – and we’re a certified Great Place to Work, too. We’re also ISO 27001, ISO 9001 and Cyber Essentials Plus certified, and hold ISO 14001 & Green Mark certifications. Our commitment to environmental sustainability sits more »

manufacturing. Maintain accurate documentation and lab records. Introduce innovative technologies and make informed recommendations. Manage project scopes, resources, and budgets effectively. Ensure compliance with ISO 13485 standards. Requirements: Essential: Bachelor's degree or higher in a biological-related discipline, with significant post-qualification experience. Minimum of 3 years' experience … in people management. Proven ability to lead, motivate, and mentor a team of scientists. Thorough understanding of product design control and ISO 13485 regulations. Extensive experience in molecular biology techniques such as FISH, PCR, DNA manipulation, and fluorescent labelling. Previous work in a regulated, diagnostic environment. Strong project management … software tools such as BLAST/BLAT and sequence searching methods. Comprehensive knowledge of genomic principles and databases. Additional management experience preferred. Experience in ISO 9001 and ISO 13485 compliant environments, including participation in audits. If you are ready to make a significant impact in a research more »

and Project, Atlassian JIRA and Confluence, ERPs, etc. Desirable • Knowledge of using Agile/Scrum for delivering work packages • Experience of working within an ISO 9001 Quality Management System • A formal Project Management qualification (e.g. PRINCE2, MSP, PMQ, etc more »

be a commercial success. .Sound knowledge of MHRA/EMA and FDA regulatory environments and requirements. Familiar with global standards related to quality e.g. ISO 9001. Confidence and ambition to provide pragmatic and considered GMP advice. High level interpersonal, communication (oral and written) skills. Accurate with strong attention to more »

not take No for an answer if we can improve Quality and will strive to have high Quality standards. Strong knowledge of Quality Standards: ISO 9001 Series Proven problem-solving skills, analytical and systematic working approach Extensive knowledge and application of the Quality discipline within Projects and Operations 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 »

device technical files and documentation for new products, working closely with Sales and Purchasing to resolve technical questions. Requirements: Experience in document control for ISO9001 Quality Management System and understanding of medical regulatory standards. Excellent computer literacy with proficiency in Microsoft Office products is essential (especially Word and Excel). 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 »

relevant SHE & Gas industry experience. Membership of a safety or environmental professional body or engineering institute to incorporated or chartered level Formal auditor training ISO 9001/14001/18001 trained more »

our unique understanding, total commitment and positive engagements We get recognised in a number of different ways: With a Glassdoor score of 4.1 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 »

construction work in the industry. A safety qualification such as CITB SMSTS is required as will experience of working with the CDM regulations and ISO9001 quality processes. A qualification in Project Management (Association for Project Management - APM or Prince 2 for example) is desirable. Knowledge of Primavera P6, and the more »

is advantageous. Proven experience (2+ years) in quality management or a related role within the construction industry. Understanding of quality standards, regulations, and methodologies (ISO 9001 etc.). Excellent communication skills. Ability to work independently and collaboratively within cross-functional teams. Knowledge of concrete pre-cast would be more »

Essential) About the Employer DALAU LTD Dalau Ltd are a market leader in the manufacture of precision plastic components & fluoropolymer products, accredited to AS9100, ISO9001, IS013485, ISO14001 & IS045001. We are based in Clacton-on-Sea - manufacturing and distributing worldwide for over 60 years. Dalau Ltd are a renowned supplier of 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 »

management, as well as the ability to understand and communicate requirements from high-precision engineering drawings Prior knowledge of Lean Manufacturing as well as ISO 9001 - Any knowledge of ISO14001 would be highly advantageous A full - clean UK driving licence will be required for the successful candidate The 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 »

that materials are available at the machine, in the correct quantities and to the correct specifications Monitor product standards and implement quality control programmes - ISO9001, ISO14001 and Q1 Carry out preventative maintenance on machines ( including lubrication, checking levels) and report any foul. Provide your own tools and ensure they are 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 »

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 »