QC Analytical Scientist

Play a key role in ensuring quality and compliance in a cutting-edge laboratory environment.

A leading organisation in the biotechnology sector is seeking a QC Analytical Scientist to support quality control testing activities within a regulated laboratory environment. This role plays a key part in ensuring product quality, safety, and adherence to regulatory standards within a fast-paced, highly regulated setting.

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

Responsibilities:

• Perform testing of gene therapy products in accordance with product specifications and GMP requirements.
• Support environmental monitoring schedules and facility-related testing activities.
• Operate and maintain laboratory equipment, ensuring proper calibration and readiness.
• Record and investigate out-of-specification (OOS) results and non-conformances, implementing corrective actions where required.
• Assist in the development and maintenance of SOPs and laboratory documentation.
• Maintain effective communication within the Quality Control team and ensure accurate document control.
• Complete required training and support training initiatives for team members.
• Ensure QC facilities remain compliant with GMP standards and support inspections or site visits.
• Contribute to the maintenance of the Quality Management System and ensure data integrity.
• Support internal and external audits.
• Assist in introducing new analytical methodologies.

Key Performance Indicators

• Timely completion of QC testing in line with production schedules and KPIs.
• Effective planning, tracking, and completion of training.
• Maintenance of laboratory environments in compliance with GMP standards.

Key Competencies

• Analytical Thinking: Ability to interpret complex data and support decision-making.
• Problem Solving: Identifies issues efficiently and implements effective solutions.
• Collaboration: Works effectively within teams and supports cross-functional activities.
• Quality Focus: Demonstrates accuracy, attention to detail, and commitment to continuous improvement.
• Communication: Strong verbal and written communication skills.
• Professionalism: Maintains accountability, integrity, and respect in all interactions.

Key Requirements

• Degree in a scientific discipline (e.g., Human Health, Life Sciences) or equivalent experience in a regulated industry.
• Experience working in GMP environments and quality control functions.
• Knowledge of EU and FDA regulations, GMP/GLP/GCP standards, and continuous improvement methodologies (e.g., Lean, Six Sigma).
• Proficiency in Microsoft Office applications (Word, Excel, PowerPoint).

About the Role

You will join a collaborative and high-performing team focused on maintaining the highest quality standards for advanced therapy products. The organisation offers a modern working environment, strong focus on professional development, and opportunities to grow within the pharmaceutical and biotechnology industry.

For more information, please contact Timi Asseez.

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.

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