Quality Technician - Castle Donington
Client:
Medstrom Location:
Castle Donington, United Kingdom Job Category:
Other EU work permit required:
Yes Job Reference:
48de9be62c6f Job Views:
54 Posted:
22.01.2025 Expiry Date:
08.03.2025 Job Description:
Your Role: Support the implementation and maintenance of the ISO13485 QMS, ensuring all processes comply with the standard’s requirements. Assist in the development, review, and revision of quality system documentation, including procedures, work instructions, and forms. Manage and maintain quality records, ensuring accuracy, completeness, and accessibility. Conduct internal audits to identify and address potential non-conformances in the QMS. Support preparation for external audits by regulatory bodies. Analyse quality data and participate in corrective and preventive action (CAPA) activities. Stay up-to-date on regulatory requirements for medical devices, including ISO13485 and relevant regional regulations (e.g. Medical Device Regulations). Contribute to continuous improvement initiatives within the QMS. Additionally, you will: Manage any complaint investigations. Co-ordinate supplier audits. Support risk management activities. Monitor quality data for each site. Review Device History Records (DHR’s). Facilitate non-conformance audits. Experience Required:
To be considered as a Quality Technician, you will need: A strong level of IT literacy with experience of common desktop applications including Excel and Word. Experience working within a QMS environment, ideally in the medical device industry. The ability to work in a fast-paced environment with strict deadlines. The ability to generate detailed, high-quality documentation. The ability to perform and/or manage multiple tasks in parallel. Excellent interpersonal skills with the ability to collaborate with others. To be detail-oriented and strive for continuous improvement. In addition to the salary and related benefits, you will join a company that has grown extensively within the last 5 years and through our unique ownership model is continuing to grow, whilst offering great career opportunities for those that are keen to progress. Standard working hours are 37.5 per week, Monday to Friday, approx. 8.30am – 5pm, with flexible hybrid working available once trained.
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Medstrom Location:
Castle Donington, United Kingdom Job Category:
Other EU work permit required:
Yes Job Reference:
48de9be62c6f Job Views:
54 Posted:
22.01.2025 Expiry Date:
08.03.2025 Job Description:
Your Role: Support the implementation and maintenance of the ISO13485 QMS, ensuring all processes comply with the standard’s requirements. Assist in the development, review, and revision of quality system documentation, including procedures, work instructions, and forms. Manage and maintain quality records, ensuring accuracy, completeness, and accessibility. Conduct internal audits to identify and address potential non-conformances in the QMS. Support preparation for external audits by regulatory bodies. Analyse quality data and participate in corrective and preventive action (CAPA) activities. Stay up-to-date on regulatory requirements for medical devices, including ISO13485 and relevant regional regulations (e.g. Medical Device Regulations). Contribute to continuous improvement initiatives within the QMS. Additionally, you will: Manage any complaint investigations. Co-ordinate supplier audits. Support risk management activities. Monitor quality data for each site. Review Device History Records (DHR’s). Facilitate non-conformance audits. Experience Required:
To be considered as a Quality Technician, you will need: A strong level of IT literacy with experience of common desktop applications including Excel and Word. Experience working within a QMS environment, ideally in the medical device industry. The ability to work in a fast-paced environment with strict deadlines. The ability to generate detailed, high-quality documentation. The ability to perform and/or manage multiple tasks in parallel. Excellent interpersonal skills with the ability to collaborate with others. To be detail-oriented and strive for continuous improvement. In addition to the salary and related benefits, you will join a company that has grown extensively within the last 5 years and through our unique ownership model is continuing to grow, whilst offering great career opportunities for those that are keen to progress. Standard working hours are 37.5 per week, Monday to Friday, approx. 8.30am – 5pm, with flexible hybrid working available once trained.
#J-18808-Ljbffr
