GMP QC Analytical Scientist — Gene Therapy Focus

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

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.