1 to 9 of 9 QA Jobs in Wales with Remote Work Options

authorities, including 510(k), PMA, CE Mark, and international submissions. Work with cross-functional teams to resolve compliance issues and deviations. Collaborate with the Quality Assurance team to ensure that the quality system aligns with regulatory requirements (ISO 13485, FDA QSR, etc.). Coordinate and participate/host internal and more »

stories to document components. 3. Provide high level of technical input when breaking down problems - help the team create customer value. 4. Contribute to quality assurance through test automation tools (Unit testing, automation testing like Cypress, Playwright) and Continuous Integration tools (Github Actions) 5. Collaborate with the product owner and more »

and trends Successful applicants will undergo a standard recruitment process, including a Welsh language test and an open book assessment. The role involves occasional quality assurance checks and offers long-term employment opportunities. Why Join the TELUS International AI Community?: Earn Extra Income Access To Our Community Wellbeing Initiative Remote more »

in order to respond to fast paced development needs. JOB PROFILE You will be working within a Scrum team made up of Developers and QA engineers, developing and unit testing REST based APIs which are used to access, retrieve, and format data from a variety of internal and external data … services such as Lambda and ECS. • Continuous Improvement: Recommend and implement enhancements to our tools and applications in order to enhance the Creditsafe offerings. • Quality Assurance: Maintain high standards for software quality and work on continuous improvement of system design and architecture. Review code for potential improvements and collaborate with more »

who has: Minimum A level or equivalent in a Science/Engineering/Quality orientated qualification Minimum of 3 years experience working in a QA/QS environment, preferably within the medical device or pharmaceutical industry. Knowledge of ISO13485:2003 and Medical Device Directive MDD 93/42/EEC more »

and sponsorships. RESPONSIBILITIES: The role is to manage different parts of construction projects, supervising crew members, preparing estimates for time and material costs, completing quality assurance, observing health and safety standards and ensuring these are upheld, and compiling reports for different stakeholders. The project involves the design, construction, finance, and more »

programs that align with industry regulations and company policies. Key Responsibilities: Regulatory Compliance: Ensure all medical devices comply with relevant international and local regulations. Quality Assurance: Collaborate with the quality assurance team to conduct internal audits, manage non-conformance's, and implement corrective actions. Product Development Support: Provide regulatory guidance more »

who has: Minimum A level or equivalent in a Science/Engineering/Quality orientated qualification Minimum of 3 years experience working in a QA/QS environment, preferably within the medical device or pharmaceutical industry. Knowledge of ISO13485:2003 and Medical Device Directive MDD 93/42/EEC more »

Job Title : Quality Assurance Manager Location : Mold Salary: £30,000 to £45,000 + bonus Job type: Full time - Permanent The Important Bit - The Package Competitive Salary in the region of £30,000 to £45,000 negotiable dependent on experience plus performance related bonus Company vehicle, laptop and mobile phone … birthday Regular team building days/nights out Quarterly Employee performance recognition awards Early finish on a Friday Company pension Christmas bonus The Role - Quality Assurance Manager Reporting to the Quality Manager and Company Directors, as the National Quality Auditor you will be a highly organised and proactive individual. You more »