25 Permanent ISO 9001 Jobs in the East of England

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 »

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 »

Support and Through Life Support Good understanding of Safety & Environmental management processes Good understanding of Quality Control management processes & familiar with working in an ISO 9001/ISO 27001 environment Strong communication & interpersonal skills. Personal Behaviours : Desire to provide excellent service and produce best in class service. 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 »

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 »

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 »

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 »

of our unique understanding, total commitment and positive engagement. We get recognised in a number of different ways: With a Glassdoor score of1 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 »

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 »

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 »

our unique understanding, total commitment and positive engagement. 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 »

quality sign off · Regularly assess the businesses metrology capability in terms of equipment and personnel · Knowledge of a compliance system to maintain quality standards (ISO9001, AS9100, etc) · Continuous development of departmental operations · Assist in internal & external Quality audits/visits Requirements · Contribute to the preparation and completion of quality documentation more »

multimeters and oscilloscopes Analysis of test results and presentation of the information extracted, with a solid grasp of relevant statistical methods Working in an ISO9001:2015 quality system Working to lab protocols, procedures and health and safety regulations Knowledge and experience in these areas would be an advantage: Working in more »

in Hertfordshire will have the following qualifications/experience: - Previous proven experience within a similar role within a fast-paced manufacturing environment - Experience with ISO9001, ISO13485, TUV, UL Standards - Knowledge of electronic systems and components, associated costs/pricing and influencing factors - Ability to read, understand and extract technical information more »

with platform security features - GIT version control – managing and improving control flow and processes - 3rd line architectural support - Leading and mentoring less experienced members - ISO9001, ISO27001, PCI-DSS adherence DevOps Engineer/Platform Architect – the person: It is critical you have specialised skills in the entire LAMP stack and Docker more »

Bank Holidays. Company Pension. PPE supplied. Company Profile An established specialist, subcontract manufacturer of precision machined components to various industry sectors, certified to AS9100and ISO9001 standards with capabilities in CNC Milling, CNC Turning, EDM and Subcontract Inspection are experiencing considerable growth and expansion. Job Profile Due to this growth, expansion more »

ISO9000 terminology. • Can deliver reports orally and written in an objective manner. • Fully proficient in modern office computer systems and technology ie: office 365. • ISO 9001 :2015 lead auditor trained. Duties for Quality Engineer role: • To support the co ordination, submission, compliance and management of all assurance activities more »

considered for the Principal Test Engineer vacancy you must have: Prior experience in a related position/field Knowledge of quality systems such as ISO9001:2015 Experience with both LabVIEW and Python Experience with complex electronics testing An understanding of sensor technology (ideally MEMS/gas sensors) If you have more »

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 company's ISO compliance program Collaborate with other functional areas in the investigation … compliance system. COMAH environment experience preferable. Advanced IT skills for data management, reporting and system administration. Recognised internal auditing training/qualification for ISO9001, 14001 and 45001. Hours: Monday to Friday: 9am-5.30pm more »

documenting the results ? Monitoring production compliance within safety, quality and regulatory requirements ? Performing tooling, equipment, system and manufacturing validations ? Generating documentations adhering to all ISO requirements … Providing and working to strong CI improvements and developments for the team. Skills required ? Certified qualification in validation and verification ? Internal auditing qualification to ISO9001 practises ? Six sigma experience and leadership skills ? Working experience of MiniTab or similar Please apply for this role by sending a CV to or call … and ask for Julie. Skills Required validation, manufacturing, ISO practices, running tests and analysing data, CI, six sigma, Qualifications Required own transport Keywords validation, manufacturing, ISO practices, running tests and analysing data, CI, six sigma more »