Senior Quality Manager (Pharmaceutical)

Zenopa; Greater London; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading UK-based healthcare organization is looking for a Senior Quality Manager in London. This position will involve taking on strategic responsibilities while ensuring compliance with regulations. The successful candidate will act as the Responsible Person under GDP requirements, review batch release documentation, and manage the Quality Management System. They will liaise with Contract Manufacturing Organisations, focusing on technical oversight to improve quality functions. This role is ideal for results-driven professionals seeking impact in a dynamic environment.

Qualifications

• Experience with GDP requirements and acting as Responsible Person.
• Proven track record in managing Quality Management Systems.
• Ability to liaise effectively with Contract Manufacturing Organisations.

Responsibilities

• Act as the Responsible Person under GDP requirements.
• Review batch manufacturing documentation for QP release.
• Manage and improve the Quality Management System while ensuring MHRA compliance.
• Provide oversight on technical matters and investigations with CMOs.

Skills

Quality Management

Regulatory Compliance

Batch Release Oversight

Operational Excellence

Job description

Since 2022, the company has launched around 20 products and maintains an active development pipeline of approximately 50 more. целей>

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.

• 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. subsystem>
• 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; laboratory management is not required, as the internal lab team operates independently.

Quality Manager • London, United Kingdom