We are working with a dynamic and innovative company based in Suffolk, looking to expand their team with a talented individual who possesses a strong background in manufacturing medical devices, expertise in ISO13485, and a relevant education within the industry.
Are you an experienced and driven Medical Device Project Engineer seeking a new and exciting opportunity?
Responsibilities
Lead and manage medical device projects from conception to completion, ensuring adherence to timelines, budgets, and quality standards.
A long term Medical Device client of ours based in West Yorkshire, are looking to add a Regulatory Specialist to their team to support their growing business.
Responsibilities will include: Provide technical support to the business, suppliers and customers on all matters relating to the safety, legality and quality of the products purchased and sold.
They are looking for an individual that is hard working and self-motivated to assist with all things regulatory.
After raising a pre-seed round in early 2023 and validating the technology through hospital trials, they are poised to launch its first product by the end of 2024.
Over the past decade, the company has pioneered a unique technique that measures the electrical properties of individual bacteria, enabling much faster detection of antibiotic susceptibility or resistance compared to traditional methods.
We're seeking a Lead Software Engineer to design and implement both software and firmware, while also overseeing the user interface design for our products.
Are you a Quality Engineer or similar from a Medical /Engineering / Science/ Biological background looking for an exciting opportunity to work for a company that use cutting edge technology to produce life changing equipment globally who work with some of the largest companies in the UK such as the NHS and provide a range of potential to progress into senior roles and specialist training on medical equipment?
£35,000 - £45,000 Flexible working Hybrid Working Company Pension Training Progression Company Benefits
Perform scheduled preventative maintenance on medical equipment, strictly following manufacturer's guidelines.
General
Biomedical Engineer - LONDON - on site
We are recruiting for an enthusiastic individual to lead on-site medical device repairs, preventative maintenance, and asset management at a cutting-edge hospital location.
Collaborate with a cross-functional team to develop a transcatheter heart repair device.
General
Job Description: We're seeking a Senior Quality Engineer to support the development of a cutting-edge structural heart device.
You will oversee design, verification, validation, clinical trials, and regulatory compliance to ensure the product meets the highest standards whilst reporting to the QA Manager.
The role as Validation Engineer will give you the opportunity to work on novel and complex medical devices whilst working closely with R&D Engineers, external consultants, and suppliers to ensure the company's reputation and quality of products remain market leading.
A growing medical devices company based in Cambridgeshire are in the process of expansion and are actively looking for an experienced Validation Engineer to join the team.
Your work will be vitally important in ensuring the successful execution of validation and verification activities required ahead of regulatory approval, product launch, and mass manufacturing.