- Understand technical and user requirements of the products.
- Create, debug, test, document, and deploy software for new products, including software/hardware interfaces, user interfaces, data logging and presentation.
- Work with the existing software development team.
- Follow all relevant medical device directives and EU GMP Annex 11 with regards to software.
- Keep relevant Quality Management System documentation up to date.
- 2+ years of experience creating software for a regulated field such as medical devices.
- 2+ years of experience in writing code in C/C++ and Python.
- Experience of software development with a strong focus on embedded systems.
- Experience of electronics, including microcontrollers.
- A software, electronics or computer sciences degree from a leading university (or equivalent).
- Experience of machine vision systems and image recognition would be beneficial.
- Experience of writing code for systems and control engineering.
- Experience with Linux distributions such as Ubuntu would be beneficial.
- Experience with real-time operating systems such as FreeRTOS would be beneficial.
- Experience of designing software that interacts with electromechanical and/or fluid systems and hardware and be able to resolve problems at the interface of these systems would be beneficial.
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Software Engineer - Stevenage, United Kingdom - MFX
Description
Job Description
Overview of the Role at MFX:
The Software Engineer will design and implement software solutions for all aspects of the products. They will assist software development within the team, ensuring best practices to medical device and GMP standards where appropriate.
The software engineer at MFX will be a key player in advancing the revolutionary bioprocessing platform for the Cell and Gene Therapy (CGT) market. This transformative technology aims to enable ultra-low-cost and scalable CGT production, expediting the journey from discovery to commercialization with unprecedented efficiency. Joining MFX
presents a unique opportunity to shape the future of bioprocessing technologies, contributing to the vision of making advanced therapies more accessible and cost-effective for a broader patient base while significantly reducing development timelines.
Responsibilities and duties:
Qualifications & Experience:
