Quality Assurance Engineer - Medical Devices
Newton Colmore is working with a medical devices company in the West Midlands, and we are assisting them with their search for a quality assurance engineer to work on a contract basis. This is a key role within the organisation and the contract is anticipated to last around six months. The company is happy for you to work remotely, but there will be occasions where you will need to be onsite. Across quality and regulatory affairs, you will be working on the document control process, the supplier process, the translation process, and the registration process in this all-encompassing role. You will be working closely with the head of the team, the senior quality engineer, and the design team to ensure all things QARA are adhered to and all processes that can be improved are improved. To be considered for the QA role, you will need to have prior experience within medical devices and significant exposure to electronic document management systems/QMS. Any knowledge of Regulation (EU) 2017/745 would be beneficial, and the role would be perfect for someone who enjoys working within a small team. Ideally, you will already have a limited company setup for your contracting work. The company is flexible on the experience level the candidate can bring, and they are also flexible on the day rate on offer. They can therefore tailor an offer to suit the right candidate's expectations. In regard to the process, there is a two-stage interview process where you will be invited to showcase your skills and experience while finding out more about the company, their mission, and what they can offer you. To enter the recruitment process, click apply now, and if you have the right skills and expertise, I will be in touch to discuss the opportunity further. Keywords: Medical Devices, Quality Engineer, Quality Control, ISO 13485, QMS, Project Engineer, ISO 14971
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Newton Colmore is working with a medical devices company in the West Midlands, and we are assisting them with their search for a quality assurance engineer to work on a contract basis. This is a key role within the organisation and the contract is anticipated to last around six months. The company is happy for you to work remotely, but there will be occasions where you will need to be onsite. Across quality and regulatory affairs, you will be working on the document control process, the supplier process, the translation process, and the registration process in this all-encompassing role. You will be working closely with the head of the team, the senior quality engineer, and the design team to ensure all things QARA are adhered to and all processes that can be improved are improved. To be considered for the QA role, you will need to have prior experience within medical devices and significant exposure to electronic document management systems/QMS. Any knowledge of Regulation (EU) 2017/745 would be beneficial, and the role would be perfect for someone who enjoys working within a small team. Ideally, you will already have a limited company setup for your contracting work. The company is flexible on the experience level the candidate can bring, and they are also flexible on the day rate on offer. They can therefore tailor an offer to suit the right candidate's expectations. In regard to the process, there is a two-stage interview process where you will be invited to showcase your skills and experience while finding out more about the company, their mission, and what they can offer you. To enter the recruitment process, click apply now, and if you have the right skills and expertise, I will be in touch to discuss the opportunity further. Keywords: Medical Devices, Quality Engineer, Quality Control, ISO 13485, QMS, Project Engineer, ISO 14971
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