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medical device assembler jobs in Cardiff
Senior Systems & Regulatory Software Engineer Medical Devices | High Salary or High-Rate Contract | Kent | Remote We are seeking an experienced Technical Expert to join our global team, working with active medical devices under MDR 2017/745 and ISO 13485 standards Electrionics device and audit experience is recognised. This is a fully remote role, offering the flexibility to work from...
A leading medical device manufacturer based in South Wales is seeking a Regulatory Specialist to join its Regulatory Affairs team.This is an excellent opportunity to be part of a growing, multinational organisation with a diverse portfolio of medical devices marketed globally.As a Regulatory Specialist, you will play a key role in supporting global product registrations and maintaining technical...
The Beauté Group is growing fast and we’re now looking for a commercially driven BDM to take ownership of new business sales for our aesthetic device portfolio, including INDIBA distribution and Lumi SKN devices. This role is not for someone who needs all of their leads handed to them. It is for someone who knows how to open doors, build relationships, and close high-ticket sales in the...
A leading medical device manufacturer is seeking a Senior Quality Design Engineer to lead quality initiatives in new product development and design change activities. The ideal candidate has over 5 years of experience in the medical device industry, with in-depth knowledge of ISO standards including ISO 13485 and ISO 14971. The role involves mentoring teams, leading risk management reviews, and...
A leading medical device company in Cardiff seeks a Supplier Quality Engineer to manage supplier audits, ensure compliance with quality systems, and work closely with suppliers. Ideal candidates will have experience in supplier management within regulated industries and possess strong communication and organizational skills. The role involves regular travel and offers benefits such as blended...
A pioneering medical device manufacturer in Cardiff is seeking an experienced Quality Engineer to enhance quality processes and documentation. This role involves executing quality planning, risk management, and supporting technical documentation for innovative medical devices. Candidates should hold an HND in engineering or a related field and ideally have experience in quality control within...
You will be responsible for overseeing all phases of product engineering, new product development and production support for our Automotive Mosfet product line.
A quality engineering firm in Penarth seeks a Quality Engineer to develop inspection plans and train quality control staff. Responsibilities include creating quality assurance documentation, conducting inspections, and ensuring compliance with industry standards. Ideal candidates should have experience in medical device manufacturing and validation processes. This position offers a pivotal role...
Verification & Validation Engineer (Training into Medical Devices) Competitive Salary + Technical Training + Career Progression + Autonomy + Hybrid Working + Flexi-time + 10% Pension + 33 Days Holiday Commutable from Cardiff, Newport, Bridgend, Barry, Caerphilly and surrounding areas. Are you from a Verification / Compliance / Technical Standards background within a highly regulated industry...
My client is looking for a Principal Semiconductor Packaging Engineer to lead the development of next-generation 2.5D and 3D packaging technologies. What you’ll do: - Architect innovative 2.5D/3D packaging solutions from concept to prototype. - Lead advanced packaging R&D programmes and technology roadmaps. - Oversee design, assembly, test, and validation of complex semiconductor packages. -...
A leading medical device manufacturer based in South Wales is seeking a Senior Quality Design Engineer to join its RAQA team. This senior role provides quality leadership across new product development (NPD) and design change activities, with a strong focus on risk-based thinking, prevention, and continuous improvement. Working closely with R&D, Clinical, Operations, and other functions, you...
A leading medical device manufacturer based in South Wales is seeking a Regulatory Specialist to join its Regulatory Affairs team. This is an excellent opportunity to be part of a growing, multinational organisation with a diverse portfolio of medical devices marketed globally. As a Regulatory Specialist, you will play a key role in supporting global product registrations and maintaining...
We’re hiring a Senior Quality Assurance Specialist known as a Quality Senior Scientist internally Location: Chippenham, Wiltshire, 2 days a week hybrid Contract: Fixed-Term Contract (12 months) Reports to: Scientific Affairs Director – Pharma Division Are you passionate about driving quality excellence in healthcare? Do you thrive in a regulated environment where your expertise directly...
Vishay manufactures one of the world's largest portfolios of discrete semiconductors and passive electronic components that are essential to innovative designs in the automotive, industrial, computing, consumer, telecommunications, military, aerospace, and medical markets. We help the world's most in-demand technologies come to life. Every day our products touch your life and the lives of people...
About Hydrokem Aerosols Ltd: Hydrokem Aerosols are located on the Wirral and specialise in the manufacture of aerosol and bag on valve products. We supply to a wide range of market sectors including personal care, healthcare/medical devices, veterinary, household, automotive and technical. Hydrokem Aerosols is a part of Clinimed Holding Limited, a group of companies founded in 1982 following...
About Yuwell Yuwell Medical is a global leader in healthcare solutions, committed to improving patient outcomes through innovative medical technologies. With 25 years of expertise and a strong international footprint, we deliver advanced products across homecare and clinical environments. Our mission is to build a comprehensive health ecosystem by integrating cutting-edge technology with...
You will work closely with product and technology teams to translate regulatory requirements into structured, automated logic that drives an advanced compliance platform. Key Responsibilities • Maintain and expand regulatory intelligence systems across multiple sectors • Translate regulatory requirements into workflows, automation logic, and structured rules
Senior Quality Engineer Medical Device Startup | £60M Raised Why This Role Matters This is a rare opportunity to join a high-growth medical device startup that has raised £60M from top-tier investors and is scaling rapidly towards global commercialisation. The company is building next-generation medical technologies that will meaningfully improve patient outcomes. As Senior Quality Engineer,...
You will be responsible for overseeing all phases of product engineering, new product development and production support for our Automotive Mosfet product line.
A leading medical device manufacturer is seeking a Regulatory Specialist to join its Regulatory Affairs team. This role involves maintaining technical files, preparing regulatory documentation, and supporting EU MDR and UKCA submissions. The ideal candidate will have 3-5 years of relevant experience and a degree in a scientific or engineering discipline. This position offers the opportunity to...