QC Analytical Scientist

R&D Partners; Greater London; On-site; GBP 30,000 - 48,000; Full time

Job summary

R&D Partners is seeking a QC Analytical Scientist to support quality control activities for advanced biological products. This role ensures GMP compliance and contributes to high-quality pharmaceutical production, working with the Quality Control team in the lab and assisting with audits and inspections.

The successful candidate will maintain regulatory standards, support lab operations, and collaborate with production teams, with a focus on data integrity and documentation.

Qualifications

• Experience working in health sciences or a related regulated industry.
• Familiarity with GMP, GLP, and quality control processes in pharma/biologics.
• Knowledge of EU and FDA regulations and quality standards.
• Proficiency in Microsoft Office tools (Word, Excel, PowerPoint).

Responsibilities

• Test gene therapy products and materials to ensure they meet specifications.
• Support environmental monitoring and facility management activities.
• Operate and maintain laboratory equipment with proper calibration.
• Document and investigate issues, implement corrective actions.
• Update SOPs and lab documentation as needed.
• Ensure timely completion of training and assist in training others.
• Maintain the laboratory to meet GMP standards and prepare for audits.
• Support the Quality Management System by managing documents and data integrity.
• Contribute to new testing methods for gene therapy products.
• Collaborate with production teams and respond to managerial requests.

Skills

GMP & GLP

Quality control

Regulatory knowledge

Microsoft Office

Problem solving

Team collaboration

Communication skills

Tools

Laboratory equipment

Job 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.

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