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QC Analytical Scientist

QC Analytical Scientist

Reference: BBBH29801
Date posted: 09/11/2026
Job details
Specialism
Technical Operations
Expertise
Discovery/R&D
Location
London, London, England
Job type
Permanent
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Description

Are you a QC scientist with a passion for ensuring quality and compliance in a GMP-regulated environment?

R&D Partners is seeking a QC Analytical Scientist to support quality control activities for advanced biological products and related materials. This role is responsible for ensuring compliance with GMP requirements and contributing to the consistent delivery of high-quality pharmaceutical products. Working closely with the Quality Control team, you will support laboratory operations, maintain regulatory standards, and assist with audits and inspections.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Test gene therapy products and materials to ensure they meet required specifications.
  • Support environmental monitoring and facility management activities.
  • Operate and maintain laboratory equipment, ensuring proper calibration and functionality.
  • Document and investigate any issues, implementing corrective actions as needed.
  • Assist in updating standard operating procedures (SOPs) and other lab documentation.
  • Ensure timely completion of training and assist in training other team members when required.
  • Maintain the laboratory to meet GMP standards and prepare for audits or inspections.
  • Support the Quality Management System by managing documents and ensuring data integrity.
  • Contribute to the introduction of new testing methods for gene therapy products.
  • Collaborate effectively with production teams and respond to managerial requests.

Key Skills and Requirements:

  • Previous history working in health sciences or a related field, or equivalent experience in a regulated industry.
  • Familiarity with GMP, GLP, and quality control processes in pharmaceuticals or biologics.
  • Knowledge of EU and FDA regulations and quality standards.
  • Proficiency in Microsoft Office tools (Word, Excel, PowerPoint).
  • Strong problem-solving, organizational, and communication skills.
  • Ability to work collaboratively in a team environment and adapt to changing priorities.
  • Commitment to maintaining high standards of professionalism, accuracy, and compliance.

For more information, please contact Jessica Taylor.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/

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Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

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