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Medibeam

Quality Associate

Swindon
£33k – £38k/yr
Posted about 15 hours ago
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If you are tired of being kept in one narrow lane when it comes to your quality role, this is the medical device role that finally lets you work across the whole quality system whilst continuing to grow in other areas.

A Swindon based MedTech company have created a new QARA Associate role, due to the small team being stretched with the existing work load. I know what you're thinking... really? A business that actually listens and gives QA more staff, shocking! But they have listened, and they get that for the business to thrive, QARA needs to work like a well oiled machine.

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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?

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your 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.

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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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This position would suit someone with 18-24 months quality experience that now wants to work with a bigger piece of the pie.

You will support the day to day rhythm of the quality system: logging and reviewing complaints, supporting CAPAs and change controls, reviewing batch records and manufacturing records, supporting the internal audits.

The team are relatively new, so some processes are still being tightened, and you are coming in to help raise the standard. It's a chance to actually shape how quality runs and be trusted from day one.

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What you will need:

  • Solid core QMS and quality assurance fundamentals
  • ISO 13485 experience from a medical device or IVD background
  • Ideally some internal audit exposure
  • Around two years in is the sweet spot

More than the paperwork side, when it comes to the individual, they want someone with drive, who picks things up and comes back with "I've got this".

This will be onsite in Swindon to start while the team settles, with hybrid on the table further down the line (up to 2 days remote)

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Skills

Quality Management Systems
Quality Assurance
ISO 13485
Internal Auditing
Complaint Handling
CAPA
Change Control
Batch Record Review
Manufacturing Records

Location

Swindon, England, United Kingdom

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