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Senior Quality Manager

Pharmaceutial & Biotechnolgy
Technical Specialist
Quality Control
Reading
£40,000 - £50,000
Quality Assurance

Role Overview

This is a strategic hire for a Senior Quality Manager, positioned to play a pivotal role in strengthening the company’s Quality function.
This position offers a unique blend of hands-on operational responsibility and strategic influence within a dynamic, growth-oriented business.

Company Information

This fast-growing pharmaceutical company has evolved from a consulting-led operation into a fully commercial pharmaceutical business with a global footprint. Since 2022, the company has launched around 20 products and maintains an active development pipeline of approximately 50 more.
Operating across multiple international markets – including the UK (supplying the NHS), Africa, Kosovo, CIS countries, the Middle East, and Vietnam – the organisation combines entrepreneurial energy with scientific rigor.
The company’s culture values passionate, results-oriented professionals who thrive in fast-paced environments, take ownership of their work, and are motivated by seeing the tangible impact of their contributions.

Role Requirements

Act as the Responsible Person (RP) under GDP requirements.
Review batch manufacturing documentation to support QP release.
Manage and continuously improve the Quality Management System (QMS), ensuring full MHRA compliance.
Liaise with approximately five Contract Manufacturing Organisations (CMOs), providing oversight on technical matters, investigations, and technology transfers.
Serve as a backup for regulatory submissions, utilising Freya software.
Focus areas include batch release and QMS oversight; laboratory management is not required, as the internal lab team operates independently.

Person Specifications

Qualified Responsible Person (RP).
Strong background in Good Manufacturing Practice (GMP) – depth of GMP experience is more critical than the recency of RP qualification.
Proven experience preparing for and confidently defending during MHRA inspections.
Demonstrated ability to interpret manufacturing data and identify root causes of technical or process issues.

Package

Competitive Salary.

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    Further Details/Cover Note

    Locations

    Aldershot
    Amersham
    Andover
    Aylesbury
    Banbury
    Basingstoke
    Bicester
    Bracknell
    Camberley
    Chippenham
    Eastleigh
    Faringdon
    Guildford
    Hemel Hempstead
    High Wycombe
    Maidenhead
    Malmesbury
    Marlow
    Newbury
    Oxford
    Reading
    Romsey
    Sailsbury
    Slough
    Southampton
    Swindon
    Winchester
    Windsor
    Witney
    Woking
    Wokingham
    Date Updated
    27 Jan 2026
    Job reference
    75207
    Categories
    Full Time
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    Why Zenopa?

    We aim to operate and maintain the following set of core values

    Group people cartoon
    01

    We liaise on your behalf

    Required equipment, e.g. cars, laptops, mobiles, we negotiate with the employer source and manage these on your behalf.

    02

    Solid Industry Relationships

    Our recruitment teams have built relationships with some of the UK’s most prestigious pharmaceutical companies

    03

    High Success Rate

    Our structured recruitment approach allows us to deliver consistently successful outcomes for both clients and candidates, supporting long-term placements and repeat partnerships.

    04

    Systems that work for you

    As an ISO 9000 organisation we have fully defined systems that are regularly audited. You can be assured we consistently following processes that deliver for all.