Arevna
Quality Assurance Specialist

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Job Title: Quality Consultant (Medical Devices)
Location: UK (On-site manufacturing focus / Hybrid)
Hourly Rate: £50-60 per hour
Sector: MedTech / Healthcare Manufacturing
Most Quality roles keep you glued to a desk reviewing change requests all day. This isn't that. If you are a quality engineer who actually likes being on the production floor diagnosing why a batch drifted, working with machine operators on root causes, and fixing systemic issues at the source this is built for you.
We are partnering with an expanding UK medical device manufacturer dedicated to complex patient care to appoint a Quality Specialist/Consultant.
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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Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
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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Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
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.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
What makes this mandate different:
- True Shop-Floor Presence: You will be the operational quality partner to Manufacturing and Engineering, tackling defect reduction, yield consistency, and 8D/root-cause investigations on the line.
- Closed-Loop Impact: You won't just log NCRs you will connect production reality back into ISO 14971 risk files and Technical File remediation (UK MDR / EU MDR).
- Pragmatic Culture: A team that uses ISO 13485 as a framework to build better products, not an excuse to create unnecessary bureaucracy.


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What you bring:
- Medical device background with solid knowledge of ISO 13485 and ISO 14971.
- Practical mastery of structured investigation tools (8D, 5 Whys, Ishikawa, FMEA).
- Experience with DHF/Technical File maintenance or audit readiness (Notified Body / BSi).
- A pragmatic, approachable style that earns credibility with manufacturing teams.
Drop me a direct message on LinkedIn or email me at js@arevna.co.uk
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Jessica, London