76 to 100 of 206 QMS Jobs in the UK excluding London

Manager. Familiarize Yourself with ISO 9001 Project Plan Identify Responsibilities, Policies, and Objectives of the Project Develop Your Project Documentation Up to Launch Quality Management System Review Performance Register for Certification Continual Improvement activities Key Responsibilities – Project Manager Quality Systems Promote Health and Safety in the workplace above everything else more »

providing administrative support to our Pathology Quality team. As part of the Quality Team, you will be responsible for maintaining aspects of the Quality Management System, which includes the documentation system, audits, and Incidents. You'll also help prepare documents when needed for the regulators in preparation for department assessments. 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 »

practice and competent in the use of customer technical databases Demonstrable experience of maintaining an internal audit programme Demonstrable experience of maintaining a quality management system Demonstrable experience of technical strategy implementation Demonstrable experience of delivery of BRC certification and/or equivalent certification standards A skilled problem solver with more »

Checking and reviewing of data in compliance with Data Integrity requirements Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner Supporting the team leader where required Skills/Experience Required: Degree or equivalent in a relevant scientific discipline Experience in more »

and validation processes to prepare the system for clinical studies and FDA approval. Implement test plans and protocols, documenting all activities within the Quality Management System (eQMS). Develop Work Instructions and Standard Operating Procedures (SOPs). Collaborate with Engineering, Manufacturing, and Biology teams to achieve regulatory submission and product more »

My Client, a successful, innovative and expanding food packaging company is looking to recruit a Technical Compliance Manager/Compliance Officer/QMS Manager for their modern site in Somerset. This is a newly created role and one which will be pivotal to the continued growth. Knowledg... more »

avoidable issues. Engage with customers to understand their weighing goals and advise on best-fit solutions. Adhere with the Company’s Quality Management System (QMS) to safeguard the quality, consistency, and reliability of our services. Care and manual handling of weights and weighing equipment. Proactively communicate timely details of appointments more »

number removed) My Client, a successful, innovative and expanding food packaging company is looking to recruit a Technical Compliance Manager/Compliance Officer/QMS Manager for their modern site in Somerset. This is a newly created role and one which will be pivotal to the continued growth. Knowledge of … BRC, Quality Management Systems QMS and ideally Packaging will be the key requirements for this role as well as a person that is happy working for a family company. This is a Monday - Friday role - Office based although must be happy spend time in the factory . Hours of work … and maintenance of data within Company database ·Support and Lead the business with technical queries Technical Compliance Officer Skills/Experience required: ·BRC experience ·QMS experience ·Competent in using Microsoft Office and Outlook, including Word and Excel. Knowledge of Cin7 helpful though not essential. ·HND or degree (or equivalent) in more »

The Quality Manager will be a key member of the SYBP Quality, Risk and Governance Team, responsible for ensuring that the Laboratory's Quality Management System functions correctly. The Quality Manager is accountable for: Ensuring the laboratory Quality Management System is designed, implemented and maintained becoming progressively more effective and … relationships with a wide range of stakeholders in order to engage with them. Experience of training and assessing staff competencies relating to the Quality Management System functions e.g. Audit, Non-Conformances, Document Control etc. Experience in administration, managing and review/approval of electronic errors and incidence records e.g. Datix more »

Ambitious and experienced engineer initially focused on nuclear-related applications, with specific involvement in an embedded team delivering a national project currently at concept phase. Background Wilde Analysis is a multi-disciplined consultancy and software channel partner, specializing in simulation more »

Cranleigh STEM is working with a medical device and diagnostics manufacturer with a global reach. We are looking for a driven production manager to join our client’s team at their site in Berkshire. As a production manager, you will more »

Job summary Technician (Medical Equipment - Community) Salary: Band 4 - £25,147 - £27,596 Job Type: Full time, Permanent Due to growth of the department, an additional post of Technician has been created. We are currently looking for a qualified technician more »

Management of the destructive and non-destructive testing activity. Management and control of the product and system auditing. Management and control of all relevant QMS systems ISO9001, ISO14001 etc. Lead and manage the development of preventative/corrective actions. Manage proactively any technical queries with customers providing all necessary guidance. more »

the department. Develop process improvements within the ISO 27001 framework to mitigate risks. Ensure commissioning activities comply with project timelines and quality management standards (QMS). Support and Communication: Communicate directly with customers to resolve problems. Assist with fault finding and analysis on live systems in a remote support capacity. more »

of the following: Good standard of education – GCSE/A-Level or equivalent Ideally six sigma green belt certified Good knowledge of ISO9001 & AS9100 QMS Standards QA experience in manufacturing setting (ideally automotive/aerospace) Understanding of QA/CI tools e.g 5 why, FMEA, DMAIC etc. Customer service oriented more »

in line with the QP/ITP schedule and are issued for inclusion in the LTR concurrent to the works completed. Undertake periodic Quality Management System audits both internal and external to ensure that the system and procedures are adhered to. Monitor Vendor Performance and carry out Supplier/Subcontractor 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 »

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 »

in an engineering and/or manufacturing environment. Conversant with the process of attaining and maintaining accreditations to ISO 9001 and ISO 45001 Experienced QMS/H&S auditor This is a great opportunity to join a fast growing SME organisation and be a key member of their Senior Management more »

and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a related field. Minimum of more »

and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a related field. Minimum of more »

compliance of product manufactured Off-Site and complete the relevant reporting on timely manner. Ensure the Subcontractors/suppliers maintain a robust documented Quality Management System that meets the requirements of the Works Information and supports self-certification. Perform frequent inspections of the construction elements to ensure their acceptance. This more »

clinical study and FDA approval. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Contribute to the development of Work Instructions and Standard Operating Procedures (SOPs). Collaborate with the Engineering, Manufacturing and Biology teams working 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 »