Senior GMP Production Scientist

Senior GMP Production Scientist

Full-Time 43200 - 72000 Β£ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead GMP production operations and supervise teams for clinical products.
  • Company: Join a top biopharmaceutical CDMO known for advanced therapies in the UK.
  • Benefits: Be part of a high-growth business with a focus on innovation and scientific excellence.
  • Why this job: Shape the future of cell and gene therapy in a collaborative environment.
  • Qualifications: Degree in Life Sciences or related field; experience in GMP environments required.
  • Other info: Equal Opportunities employer, welcoming diverse applicants.

The predicted salary is between 43200 - 72000 Β£ per year.

14644Permanent Competitive Site Based Gloucestershire, United Kingdom Updated on: 31-07-2025

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

Our client specialises in GMP manufacturing of advanced therapy and biologic products. As a Senior GMP Production Scientist, you will take the lead in supervising GMP manufacturing operations for a range of clinical products. This includes overseeing production teams, supporting technology transfer, and ensuring compliance across ATMP and biologics projects.

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

Supervise GMP cleanroom production operations, lead tech transfer activities from process development, and manage production planning for a variety of ATMP clinical products

Ensure manufacturing activities follow GMP and Product Specification Files, supporting material specification, closed processing, purification, and fill/finish operations up to 400L scale

As the Senior GMP Production Scientist you will manage documentation generation, including SOPs and batch records, and lead data collation for clinical trial regulatory submissions

Deliver training and mentoring for production teams, maintain compliance with safety procedures, and support internal and client-facing project meetings

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

A Degree or higher level in a relevant field (e.g., Life Sciences / Bioprocessing / Pharmaceutical Engineering). Extensive experience operating in GMP environments for ATMP or biologics manufacturing

Strong knowledge of GMP compliance and cleanroom production, with experience in one or more of the following: mammalian cell culture, downstream purification, aseptic fill/finish, or multi-product GMP facilities

Proven experience supervising teams, coordinating schedules, managing deviations and change controls, and supporting tech transfer and regulatory documentation

WHAT’S IN IT FOR YOU?
You will join a high-growth business with a globally recognised reputation in cell and gene therapy. As a Senior GMP Production Scientist, you will be part of a collaborative GMP leadership team shaping the delivery of clinical trial materials and next-gen therapies.

This is a unique opportunity to apply your GMP manufacturing skills in a technically advanced, purpose-driven environment focused on scientific excellence and innovation.

Key Words:
Senior GMP Production Scientist / ATMP / GMP Manufacturing / Cleanroom / Bioprocessing / Fill-Finish / Tech Transfer / Downstream / Cell Culture / Purification / CDMO / QA / QC / South West / Clinical Trial Material / Supervisory

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

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.

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Senior GMP Production Scientist employer: Hyper Recruitment Solutions LTD

Join a leading biopharmaceutical CDMO in Gloucestershire, where you will be part of a dynamic team dedicated to advancing cell and gene therapies. Our collaborative work culture fosters innovation and scientific excellence, providing ample opportunities for professional growth and development in a supportive environment. With a competitive salary and the chance to make a meaningful impact in the field of advanced therapy manufacturing, this role is perfect for those looking to elevate their career in a purpose-driven setting.
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Contact Detail:

Hyper Recruitment Solutions LTD Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Senior GMP Production Scientist

✨Tip Number 1

Familiarise yourself with the latest GMP regulations and guidelines specific to ATMP and biologics. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance and quality in production.

✨Tip Number 2

Network with professionals in the biopharmaceutical industry, especially those working in GMP environments. Attend relevant conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in the field.

✨Tip Number 3

Prepare to discuss your experience in supervising teams and managing production schedules. Be ready to provide examples of how you've successfully led tech transfer activities or handled deviations in a GMP setting.

✨Tip Number 4

Research the company’s recent projects and achievements in cell and gene therapy. Being knowledgeable about their work will allow you to tailor your conversation during interviews and show genuine interest in contributing to their success.

We think you need these skills to ace Senior GMP Production Scientist

GMP Compliance
Cleanroom Production
Bioprocessing Knowledge
Cell Culture Techniques
Downstream Purification
Aseptic Fill/Finish Operations
Technical Transfer Management
Regulatory Documentation
Team Supervision
Production Planning
Deviation Management
Change Control Processes
SOP Generation
Batch Record Management
Training and Mentoring

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights relevant experience in GMP environments, particularly with ATMP or biologics manufacturing. Emphasise any supervisory roles and specific projects that align with the job description.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for biopharmaceuticals and your understanding of GMP compliance. Mention specific experiences that demonstrate your ability to lead teams and manage production operations.

Highlight Key Skills: In your application, clearly outline your knowledge of cleanroom production, tech transfer, and regulatory documentation. Use keywords from the job description to ensure your application stands out.

Proofread Your Application: Before submitting, carefully proofread your application for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial in a GMP environment.

How to prepare for a job interview at Hyper Recruitment Solutions LTD

✨Showcase Your GMP Knowledge

Make sure to highlight your extensive experience in GMP environments, especially related to ATMP or biologics manufacturing. Be prepared to discuss specific examples of how you've ensured compliance and managed production operations.

✨Demonstrate Leadership Skills

As a Senior GMP Production Scientist, you'll be supervising teams. Share your experiences in leading production teams, coordinating schedules, and managing deviations. Use concrete examples to illustrate your leadership style and effectiveness.

✨Prepare for Technical Questions

Expect questions about cleanroom production processes, tech transfer activities, and regulatory documentation. Brush up on your knowledge of mammalian cell culture, downstream purification, and aseptic fill/finish to confidently answer any technical queries.

✨Emphasise Training and Mentoring Experience

Since the role involves delivering training and mentoring, be ready to discuss your approach to developing team members. Share specific instances where you have successfully trained others and maintained compliance with safety procedures.

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