76 to 100 of 204 QMS Jobs in the UK excluding London

environmental policies required in order to perform role as QC Analyst Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner. Attend internal and external scientific and technical meetings and conferences where appropriate Carry out general maintenance and house keeping of more »

of the relevant regulations • Provide reports to management to enable them to monitor system performance. • Review and authorise documentation and processes in the Quality Management System to ensure compliance with established quality procedures and applicable regulations and alignment with other related documentation. • Identify and collaborate in the implementation of changes more »

Quality Engineer Lead , Scientific Instrumentation Our client is looking to recruit a Quality Engineer Lead responsible for: Maintaining ISO accreditation and improving the quality management system performance Supporting a reduction in supplier quality problems and non-compliance on shop floor quality Assisting in the development and implementation of good fit more »

the administrative aspect of the Technical Department taking responsibility for the day to day management and maintenance of some or all of the following; QMS, HACCP, legislation, specifications, Technical Reports, Contaminants & Non Conformance Logs, complaints, microbiological & nutritional surveillance, this work includes data entry, trending, filing, information requests, co-ordination of more »

errors and reduce overall cost of Quality 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 as soon as possible, along with your availability and more »

compliance with quality standards. Preferred Requirements: Experience in assembly processes and quality control. Skilled in conducting comprehensive audits and implementing safety measures. Proficiency in QMS and ISO systems to drive quality enhancements. Excellent understanding of quality engineering principles and practices. Demonstrated ability to identify and resolve quality-related issues. Preferred more »

and any previous experience supporting in delivery of new product projects is highly desirable. Duties & Responsibilities: Oversee the day to day aspects of the QMS and requirements Oversee and support the wider quality team below them in the departmental structure Drive improvements/resolve issues highlighted by all audits/ more »

lab analysis Working closely with other sites for product specifications and documentation. Dealing with external stakeholders for food safety, quality and importing Maintenance of QMS Experience & Skills Required: The business is looking for an individual who has experience within the food industry. You must be able to lead, motivate 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 »

issues promptly and complete Export Health Certificates as needed. Quality Management Systems: Keep customer online systems updated, conduct GAP analysis, and ensure compliance with QMS, aiming for no customer non-conformances. If you're ready to take on this challenging yet rewarding role in a dynamic environment committed to excellence more »

and prepare comprehensive reports in accordance with design control standards. Background in the medical device sector to understand regulatory requirements and quality management systems (QMS) essential for successful product development. (ISO13485) Knowledge in mechanical engineering with a focus on testing equipment and innovation in product development. Requirements: Bachelor's degree more »

/FDA regulated environment. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Collaborate with the Engineering and quality departments to ensure test method, equipment and materials are available in line with company timelines. Analyse and 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 »

and processes regularly. Maintain and align HACCP (HACCP/TACCPVACCP) program is maintained and aligned with best practice at all times Implement and amend QMS for product standards. Ensure effective QA and Hygiene team management. Implement pest control mechanisms for food safety. Conduct trend analysis of quality issues. Manage internal more »

and processes regularly. Maintain and align HACCP (HACCP/TACCPVACCP) program is maintained and aligned with best practice at all times Implement and amend QMS for product standards. Ensure effective QA and Hygiene team management. Implement pest control mechanisms for food safety. Conduct trend analysis of quality issues. Manage internal more »

milestone progress to the Project Lead, Programme Manager and Stakeholders. Maintain best practices within the Software Team, ensuring technical journals, essential research and company QMS process are followed. Leadership and administration of the Sprint process for the Software Team. Support the delivery of product firmware and software within the Software more »

bar to make up our datalogger tools. This process requires great attention to detail due to the fine tolerances involved. • Work to all Company QMS policies and procedures as per ISO 9001:2015. • Ensure that a safe working environment is maintained at all times through compliance with Health and safety more »

and Qualifications: Demonstrated experience in the design and development of products - Medical industry advantageous Design or Engineering Degree preferred Familiarity with regulatory standards and QMS - ISO13485 advantageous CAD proficient, preferably Solidworks Plastic manufacturing process knowledge If you want to be part of a team dedicated to making a meaningful impact more »

join the company. Permanent role with a competitive starting salary and extensive benefits package. Job Overview: Maintenance and improvement of the Quality Management System (QMS). Assure the compliance of all activities with Good Distribution Practice (GDP) and Good Manufacturing practice (GMP) requirements. Responding to medical information enquiries from healthcare more »

Monitoring) for Part21J knowledge with aviation regulations, including CAA EASA, FAA. line leader for a team of Quality professionals across multiple locations. the companies QMS and quality systems. continuous improvement of Quality business systems. portfolio of external and customer Quality approvals. and conduct internal audit plans covering approvals and certification. more »

Manufacturing support to the production areas with reference to quality issues Ensuring procedures are implemented or updated where appropriate. Actively support the business with QMS to ISO 9001:2015 certification Key skills and experience for the Quality Engineer job are: Previous work experience as a Quality Engineer or similar role more »

Manufacturing support to the production areas with reference to quality issues Ensuring procedures are implemented or updated where appropriate. Actively support the business with QMS to ISO 9001:2015 certification Key skills and experience for the Quality Engineer job are: Previous work experience as a Quality Engineer or similar role more »

formal qualification in quality, although this isnt essential. About the Job Youll take the responsibility of ensuring products are manufactured meet the customer specifications. QMS maintenance that complies with ISO9001. Youll lead a small team, youll be able to influence and motivate to ensure goals are met. Youll ensure internal more »

conformances and collaborate on CAPA objectives. Working with the Leadership Teams as well as building positive and effective relationships with other internal stakeholders on QMS related activities. Ready to apply? This is what you will need to demonstrate; Qualified/Certified Auditor for ISO 13485 (please note, this is a more »

for a perm role on behalf of our client based in Stanford le Hope. Duties 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 more »