Senior QC Analytical Scientist

R&D Partners; City Of London; On-site; GBP 80,000 - 100,000; Full time

Job summary

A biotechnology organization in London is looking for a Senior QC Analytical Scientist to perform quality control testing, ensure compliance with regulatory standards, and maintain accurate documentation. This role demands high attention to detail and strong understanding of GMP and GDP principles. The opportunity is ideal for candidates passionate about quality and accuracy in their work.

Qualifications

• Passionate about ensuring accuracy and adherence to industry best practices.
• Knowledgeable in compliance with regulatory standards.

Responsibilities

• Perform quality control testing to meet targets and industry standards.
• Conduct internal audits to ensure compliance with regulations.
• Plan, manage, and document training activities effectively.
• Ensure all work complies with Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP).
• Complete assigned documentation tasks accurately and on time.
• Keep training records updated and complete necessary training.

Skills

Strong understanding of GMP and GDP principles

Ability to manage documentation and training in a regulated environment

High attention to detail

Excellent organizational and communication skills

Job description

Senior QC Analytical Scientist

Driving biotech breakthroughs with precision analytics and uncompromising quality control.

R&D Partners is seeking a Senior QC Analytical Scientist to join a biotechnology organization based in London. In this role, you will focus on quality control testing, compliance with regulatory standards, and maintaining high-quality documentation. This is an excellent opportunity for someone passionate about ensuring accuracy and adherence to industry best practices.

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

Responsibilities

• Perform quality control testing to meet targets and industry standards.
• Conduct internal audits to ensure compliance with regulations.
• Plan, manage, and document training activities effectively.
• Ensure all work complies with Good Manufacturing Practice (GMP), Data Integrity, and Good Documentation Practice (GDP).
• Complete assigned documentation tasks, such as corrective actions, change controls, and audit follow-ups, accurately and on time.
• Keep training records updated and complete necessary training before starting tasks.

Key Skills and Requirements

• Strong understanding of GMP and GDP principles.
• Ability to manage documentation and training in a regulated environment.
• High attention to detail with a commitment to accuracy and "right-first-time" execution.
• Excellent organizational and communication skills.

Contact: Jessica Taylor