Allerton Bishop Search
Qualified Person (QP) - Remote

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The Role
As the organisation continues to grow, we are seeking an experienced Qualified Person (QP) to join its UK Quality team. This is a broad and influential role combining QP responsibilities with wider quality leadership in an international environment.
You will:
- Perform QP duties and batch certification/release activities in line with applicable GMP and regulatory requirements.
- Provide oversight of key quality systems and support continued compliance.
- Lead and support deviations, complaints, CAPAs and quality risk assessments.
- Provide QP oversight of product quality reviews and activities supporting batch release.
- Support audits, inspections and inspection readiness.
- Provide GxP and quality guidance across the business.
- Work with internal teams and external partners to resolve quality issues and maintain product supply.
- Drive continuous improvement across quality processes and systems.
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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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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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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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About You
You will be an eligible Qualified Person in the UK with strong pharmaceutical industry experience and a detailed understanding of GxP and pharmaceutical quality systems.
You will ideally bring:
- A life sciences degree or equivalent relevant experience.
- Eligibility to act as a Qualified Person in the UK.
- Strong knowledge of GMDP requirements across manufacturing, packaging, licensing and batch release.
- Experience of investigations, CAPAs, risk assessment and continuous improvement.
- Experience across multiple dosage forms would be advantageous.
- Strong problem-solving, communication and stakeholder management skills.
- A collaborative approach and the ability to manage multiple priorities.


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Why Join
This is an opportunity to join an established international biopharmaceutical organisation during an exciting period of growth.
The position offers more than routine batch release, with the opportunity to influence quality systems, drive continuous improvement and gain broad exposure across an international business.
You will join a collaborative environment where your expertise can have a visible impact, with excellent opportunities to broaden your responsibilities, develop your leadership capabilities and progress your career as the organisation continues to grow.
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