SRG
Quality Control Scientist

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QC Scientist
Greater Manchester
SRG are recruiting for a QC Scientist to join a highly successful CDMO based in Greater Manchester. Growing rapidly, the business specializes in taking products from discovery, all the way through early-stage trials and to approval.
Due to continued growth and expansion of the business, they are seeking to hire a QC Scientist to join their team in Greater Manchester to support the QC testing of products and assisting with Method Development & validation activities.
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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No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Key Responsibilities
- Hands-on analysis of products using UPLC/HPLC
- Conduct routine pharmacopeial testing, including:
- IR identification
- Appearance testing
- pH testing
- Content uniformity
- Dissolution testing
- Water content analysis
- Supporting method transfers, validations, and method development activities for assays, related substances/impurities, dissolution, and cleaning validation methods.
- Supporting root cause investigations into deviations, non-conformances, and out-of-specification (OOS) results, and implementing appropriate CAPAs.


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Qualifications & Experience
- Degree in a relevant scientific discipline such as Pharmaceutical Sciences, Chemistry, Biology, or a similar experience within a related field
- Prior experience in a Quality Control role within a GMP pharmaceutical environment.
- Hands-on experience with UPLC / HPLC
- Prior experience working with Oral Solid Dose forms & Dissolution testing would be advantageous
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