The Role Supporting with the R&D functions, assisting with new product development, project management and data analysis. Working alongside product management, technical development, Qualityassurance and Operations. Organising testing and certification procedures Producing competitor research and data analysis. Will ideally have some previous experience of project management and status more »
Cardiff, South Glamorgan, Wales, United Kingdom Hybrid / WFH Options
Gyrus Medical Ltd An ATL Technology Company
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 »
days plus bank holidays additional day service related Pension Health Benefits: company currently looking at options Onsite parking, uniform Overview Are you passionate about qualityassurance? We are seeking a meticulous and experienced QA Senior Engineer/Manager to oversee the qualityassurance and quality control processes and mentor our … processes and procedures comply with regulatory standards, maintaining documentation, implementing quality improvement initiatives, and training laboratory staff on quality protocols. Responsibilities: Develop and improve qualityassurance policies and procedures to ensure compliance with regulatory requirements and industry standards (e.g. BRC, GMP) Conduct regular audits and inspections of laboratory and manufacturing … to identify trends, deviations, and potential issues, and implement corrective actions as needed. Collaborate with laboratory staff to develop and implement training programs on qualityassurance protocols and procedures. Maintain accurate and up-to-date documentation of qualityassurance activities, including audit reports, corrective action plans, and training records. Investigate more »
join an international business with a great reputation locally. Providing you with excellent stability following sustained business growth, this role will see you overseeing qualityassurance within the business being responsible for audits, compliance to international standards and responding customer enquiries. This role would be well suited to a quality … manager with experience of managing small teams within the Life Science sector. Roles and Responsibilities: Overseeing all aspects of qualityassurance for the site, ensuring compliance with regulatory requirements. Developing and maintaining an internal audit program covering regulatory compliance and quality assurance. Collaborating with cross-functional teams to identify areas … system, ensuring accuracy and reliability. Monitoring non-conformities and developing strategies for improvement. Customer audits and resolve customer complaints through root cause investigations. Requirements QualityAssurance experience - auditing, customer complaints, RCA. Experience managing a small team would be beneficial. Experience working in a highly regulated industry - pharmaceutical, medical, 24383/ more »
they are looking to take on a skilled Process Engineer and take them to the next stage of their career. On offer is a QualityAssurance Manager position, where you will take the lead and be responsible for ensuring continued compliance with quality standards, as well as developing and maintaining … step into a highly autonomous position, to play a crucial part in the success of a internationally renowned business. The Role: *Quality Management and QualityAssurance across departments on site *Ensuring quality standards and compliance is in line with regulatory requirements *Working highly autonomously and in line with the different … the site from a quality perspective. The Person: *From a Quality Background *Familiar with ISO9001 regulations *Full UK Drivers License Quality Engineer, Quality Manager, QualityAssurance, Quality Control, QA, QC, ISO9001, ISO 9001 Reference Number: BBBH228748 To apply for this role or to be considered for further roles, please click more »