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Biomedical Engineer

Computerworld Personnel Ltd

Portishead, Bristol, Cheltenham

On-site

GBP 40,000 - 50,000

6 days ago

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An established industry player is seeking a skilled Biomedical Engineer to innovate and enhance medical devices. This role involves designing cutting-edge products and ensuring they meet regulatory standards, while also providing technical support to the commercial team. With a competitive salary and a range of benefits, including a pension scheme and healthcare cash plan, this position offers a fantastic opportunity for professionals passionate about improving healthcare technology. Join a dynamic team dedicated to advancing medical solutions that make a difference in surgical procedures.

25 days holidays plus bank holidays

Pension Scheme

Healthcare cash plan

Sick Pay

Life Assurance

Degree in Biomedical Engineering or relevant experience required.
3+ years in medical device product development preferred.

Design new products and maintain the existing product range.
Provide technical expertise and create regulatory-compliant documentation.

Biomedical Engineering

Medical Device Development

Technical Documentation

Regulatory Compliance (ISO13485/21CFR820)

Degree in Biomedical Engineering

Relevant Engineering/Scientific Subject

Biomedical Engineer

South West Wales

26133/610

£40,000 - £50,000 plus further benefits

What is on offer?

A salary of up to £50,000
25 days holidays plus bank holidays
Pension Scheme
Healthcare cash plan
Sick Pay
Life Assurance

The Role:

The Biomedical Engineer will be responsible for designing new products and maintaining the current product range. The job duties of a Biomedical Engineer involve designing, developing, and maintaining cutting-edge medical accessories used during surgical procedures.

DUTIES AND KEY RESPONSIBILITIES

The design of new products for the company's product portfolio
Providing technical expertise to the commercial team in communication to and from customers
The creation of technical documentation and product technical files which conform to all regulatory requirements
Chair project and stakeholder meetings as and when required
Conduct and oversee when required product verification and validation activities

What you need?

Preferably degree educated in Biomedical Engineering or a relevant engineering / scientific subject or relative industry experience.
More than 3 years' experience of medical device product development would be preferable
Working knowledge of relevant medical device regulatory requirements (ISO13485/21CFR820, IEC 60601 etc)

If you are interested in this position please click 'apply'.

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