Senior Quality Manager (Pharmaceutical)

Zenopa; Tadley; On-site; GBP 50,000 - 70,000; Full time

Job summary

A pharmaceutical company in England is seeking a Senior Quality Manager to enhance the company's Quality functions. This role requires compliance with Good Distribution Practice (GDP) regulations and involves managing the Quality Management System (QMS). The candidate will liaise with Contract Manufacturing Organisations and ensure documentation supports batch release. This position offers both operational and strategic responsibilities within a dynamic business.

Qualifications

• Experience managing Quality Management Systems (QMS) in a regulated environment.
• Proven ability to liaise with Contract Manufacturing Organisations (CMOs).
• Strong understanding of Good Distribution Practice (GDP) requirements.

Responsibilities

• Act as the Responsible Person under GDP requirements.
• Review batch manufacturing documentation to support QP release.
• Manage and improve the Quality Management System (QMS).
• Liaise with CMOs on technical matters and investigations.
• Ensure full compliance with MHRA regulations.

Job description

Company Overview

• 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.

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.

Responsibilities

• 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.
• Focus areas include batch release and QMS oversight; laborat...