Medibeam
Quality Validation Engineer

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Quality Engineer - Process Validation
I am looking to speak with Quality Engineers who genuinely understand process validation.
Not just reviewing protocols someone else has written, but actually owning it. From concept and design, through IQ/OQ/PQ, to final release.
I’m working with a growing Medical Device manufacturer looking for someone to take real ownership of their process validation lifecycle and there’s plenty to get stuck into.
The validation process needs a few tweaks to ensure that the risk-based approach flows through properly into what actually happens on the ground, and they want someone who can come in, work out what needs improving and rebuild it properly.
Initially, around 70% of your role will be focused on validation.
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.
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.
You’ll be looking at:
- The full process validation lifecycle
- IQ, OQ, and PQ
- Risk and impact assessments
- SPC and process capability
- Measurement System Analysis
- PFMEA
- Improving templates and documentation
- Making validation genuinely risk-based, rather than a tick box exercise
The other side of the role is broader Quality Engineering.
Using data to understand how processes are actually performing and spotting problems before they become NCRs or CAPAs.
Over time, the role moves more towards oversight.
You’ll be the person setting the standard for validation and guiding teams as new equipment and processes are introduced.


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They’re not looking for someone who has supported validation from the sidelines.
You need to have owned equipment or process validation yourself, ideally within Medical Device or pharmaceutical manufacturing, and be confident taking something from concept all the way through to release.
If you’ve done that and want a role where you can actually improve how validation is done, rather than inherit a perfect system and maintain it, this could be a really good one.
Please note, this role is quality within a manufacturing environment focused on improvements to processes, so naturally it is ONSITE.
Please only apply if you're happy to be onsite 5x per week in Cambridge.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
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