GMP Production Manager

ROLE OVERVIEW

We are currently looking for a GMP Production Manager to join a leading biopharmaceutical CDMO based in the South West of the UK to join their team.

Our client supports the manufacture of cell and gene therapies and small-scale biologics for early-phase clinical trials. As a GMP Production Manager, you will lead the GMP production team and oversee the day-to-day management, scheduling, and operations of the facility in compliance with licensing and regulatory standards.

KEY DUTIES AND RESPONSIBILITIES
Your duties as the GMP Production Manager will be varied however the key duties and responsibilities are as follows:

Act as the named Production Manager on the facility’s manufacturing licence, leading GMP operations, qualification of the facility and compliance with authorised specifications

Recruit, train and manage production staff, deliver departmental training, and establish a high-performing, motivated team

As the GMP Production Manager you will oversee production planning, documentation, and process execution in line with GMP and licensing requirements

Ensure GMP compliance across cleanroom activities, drive continuous improvement, and support quality reviews and deviation management

Represent the GMP team in internal and client-facing project meetings, lead cross-functional collaboration, and support audit readiness

ROLE REQUIREMENTS
To be successful in your application to this exciting role as the GMP Production Manager, we are looking to identify the following on your profile and past history:

A Degree or higher level in a relevant subject (e.g., Pharmaceutical Manufacturing / Bioprocessing / Quality Management). Extensive experience managing GMP cleanroom operations in ATMP or biologics settings

Strong understanding of MHRA, HTA, and GMP compliance including cleanroom qualification, batch release processes, and managing multi-product facilities

Proven experience leading production teams, managing complex schedules, driving operational improvements, and supporting tech transfer and regulatory interaction

WHAT’S IN IT FOR YOU?
You will join a rapidly growing organisation with a global reputation in the CGT and biopharma sector. As GMP Production Manager, you will play a critical leadership role in delivering compliant clinical-grade materials and contribute directly to the future of advanced medicines.

This is an excellent opportunity to take ownership of facility leadership and develop a high-performing GMP manufacturing team in a purpose-driven organisation.

Key Words:
GMP Production Manager / GMP / ATMP / CDMO / Cleanroom / Manufacturing Licence / Fermentation / Fill Finish / Viral Vectors / Biopharma / SOP / Tech Transfer / South West / Clinical Trial Material / Quality Compliance

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career