GMP Production Manager

GMP Production Manager

Hounslow Full-Time 48000 - 84000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead a GMP production team and manage daily operations in a biopharmaceutical facility.
  • Company: Join a leading biopharmaceutical CDMO known for cell and gene therapies.
  • Benefits: Enjoy a full-time role with opportunities for growth in a rapidly expanding organisation.
  • Why this job: Make a real impact on advanced medicines while developing a high-performing team.
  • Qualifications: Degree in Pharmaceutical Manufacturing or related field; experience in GMP cleanroom operations required.
  • Other info: Equal Opportunities employer, welcoming applications from all qualified candidates.

The predicted salary is between 48000 - 84000 £ per year.

Direct message the job poster from Hyper Recruitment Solutions

Senior Recruitment Consultant at Hyper Recruitment Solutions – HRS

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.

Seniority level

  • Seniority level

    Mid-Senior level

Employment type

  • Employment type

    Full-time

Job function

  • Job function

    Production and Manufacturing

  • Industries

    Biotechnology Research and Pharmaceutical Manufacturing

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GMP Production Manager employer: Hyper Recruitment Solutions

Join a leading biopharmaceutical CDMO in the South West of the UK, where you will be part of a dynamic team dedicated to advancing cell and gene therapies. As a GMP Production Manager, you will benefit from a supportive work culture that prioritises employee growth and development, offering opportunities to lead a high-performing team while ensuring compliance with industry standards. With a global reputation and a commitment to innovation, this organisation provides a meaningful and rewarding environment for those passionate about making a difference in the biopharma sector.
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Contact Detail:

Hyper Recruitment Solutions Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land GMP Production Manager

✨Tip Number 1

Make sure to network with professionals in the biopharmaceutical sector, especially those involved in GMP operations. Attend industry conferences or local meetups to connect with potential colleagues and learn more about the company culture at Hyper Recruitment Solutions.

✨Tip Number 2

Familiarise yourself with the latest regulations and compliance standards related to GMP and ATMP. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high-quality standards in production.

✨Tip Number 3

Prepare to discuss specific examples of how you've led production teams and managed complex schedules in previous roles. Highlight any operational improvements you've implemented that align with the responsibilities of a GMP Production Manager.

✨Tip Number 4

Reach out directly to the job poster or other employees at Hyper Recruitment Solutions via LinkedIn. A direct message can help you stand out and show your enthusiasm for the role, making it more likely for them to remember you during the selection process.

We think you need these skills to ace GMP Production Manager

GMP Compliance
Cleanroom Operations Management
Biopharmaceutical Manufacturing
Team Leadership
Production Planning
Regulatory Knowledge (MHRA, HTA)
Quality Management Systems
Process Improvement
Training and Development
Cross-Functional Collaboration
Audit Readiness
Documentation Management
Batch Release Processes
Technical Transfer

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in GMP cleanroom operations, particularly in ATMP or biologics settings. Emphasise your leadership roles and any specific achievements related to compliance and operational improvements.

Craft a Compelling Cover Letter: In your cover letter, express your passion for biopharmaceutical manufacturing and detail how your background aligns with the key responsibilities of the GMP Production Manager role. Mention your understanding of MHRA, HTA, and GMP compliance.

Highlight Relevant Qualifications: Clearly state your degree or higher qualifications in a relevant subject. If you have additional certifications or training related to GMP or quality management, be sure to include those as well.

Showcase Leadership Experience: Provide examples of your experience in recruiting, training, and managing production teams. Highlight any successful projects where you led cross-functional collaboration or improved operational processes.

How to prepare for a job interview at Hyper Recruitment Solutions

✨Showcase Your GMP Knowledge

Make sure to highlight your understanding of GMP compliance, particularly in cleanroom operations. Be prepared to discuss specific regulations and how you've ensured compliance in your previous roles.

✨Demonstrate Leadership Experience

As a GMP Production Manager, you'll be leading a team. Share examples of how you've successfully managed production teams, including any challenges you faced and how you motivated your staff to achieve high performance.

✨Prepare for Technical Questions

Expect technical questions related to biopharmaceutical manufacturing processes, batch release, and quality management. Brush up on your knowledge of ATMPs and biologics to confidently answer these queries.

✨Emphasise Continuous Improvement

Discuss your experience with driving operational improvements and how you've implemented changes in past roles. Highlight any specific methodologies or tools you've used to enhance efficiency and compliance.

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