Cure Talent
Software Lead

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Software Lead
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Job type: Permanent
County: Leicestershire
Country: United Kingdom
Salary/rate: £75-85K (Neg. DOE)
Discipline: R&D
Job ref: CT2054
Post Date: 17-06-2026 04:20 PM
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Cure Talent are delighted to be partnered with an emerging wearable medical technology company at a defining stage of its growth.
As Software Lead, you will take ownership of software development across the company's medical device platform. You will lead multidisciplinary software teams, drive technical strategy and remain hands-on in architecture, development and problem-solving.
This is a rare opportunity to play a leading role in bringing innovative wearable medical technology to market whilst helping establish the software foundations for future products and platform expansion.
Reasons to use Rodeo
I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?
Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.
Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.
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Graduate Consultant — 2026 Scheme
Why you're a good match
StrongYour economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.
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Why you're a good match
You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.
Experience fit
Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.
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Key Responsibilities
Lead the software development of medical devices from early-stage development through to commercial release Ensure software development activities comply with IEC 62304 and support regulatory submissions, including FDA 510(k) Coordinate multidisciplinary software teams, including software engineers, algorithm developers, UI developers, SDK developers and external subcontractors Work closely with firmware, electronics and systems engineering teams to deliver integrated product solutions Remain actively involved in software architecture, technical decision-making, development and problem-solving
Experience & Skills Required
Proven experience leading software development for regulated medical devices Strong understanding of IEC 62304 and the medical device software development lifecycle Experience supporting FDA 510(k) submissions and commercial product releases Previous experience leading multidisciplinary software teams and external development partners Strong systems-level understanding and experience working across software, firmware and hardware disciplines Hands-on technical background with the ability to contribute to architecture, development and troubleshooting activities


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