Senior GMP Production Scientist

Hyper Recruitment Solutions; London; On-site; GBP 40,000 - 60,000; Full time

Job summary

Hyper Recruitment Solutions is seeking a Senior GMP Production Scientist to oversee GMP manufacturing operations in a leading biopharmaceutical CDMO. The successful candidate will supervise production teams, ensure compliance, and contribute to the manufacturing of advanced therapies. This role offers the chance to be part of a high-growth, innovative environment in cell and gene therapy.

Qualifications

• Degree or higher level in a relevant field.
• Extensive experience in GMP environments for ATMP or biologics manufacturing.
• Strong knowledge of GMP compliance and cleanroom production.

Responsibilities

• Supervise GMP cleanroom production operations.
• Manage documentation generation including SOPs and batch records.
• Deliver training and mentoring for production teams.

Skills

GMP compliance

supervising teams

cleanroom production

tech transfer

Education

Degree in Life Sciences / Bioprocessing / Pharmaceutical Engineering

Job description

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Role Overview

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.

Role Overview

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

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Staffing and Recruiting

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