QA Associate

Hobson Prior; London; On-site; GBP 30,000 - 45,000; Full time

Job summary

Join a leading biotech firm as a QA Associate in London, dedicated to advancing life-changing science. You'll be responsible for ensuring high standards in manufacturing, particularly within cell and gene therapy, and will work closely with various teams to maintain compliance and improve quality systems. This position is ideal for those with a scientific background and a passion for quality assurance.

Qualifications

• Degree in a scientific or technical field preferred.
• Experience in a GMP manufacturing environment necessary.
• Familiarity with sterile manufacturing processes is a plus.

Responsibilities

• Oversee quality assurance for manufacturing operations.
• Review and approve documents for GMP compliance.
• Conduct internal audits and manage corrective actions.

Skills

Communication

Problem-solving

Quality Assurance

GMP Compliance

Education

Degree in a scientific or technical field (e.g., Chemistry, Life Sciences)

Tools

Electronic Quality Management Systems (QMS)

Job description

Ready to play a key role in advancing life-changing science? Join our dynamic biotech team as a QA Associate and help ensure the highest standards in innovation, quality, and patient impact!

Hobson Prior is seeking a QA Associate to join a dynamic team in London. This role focuses on ensuring high-quality standards in manufacturing operations, particularly within the cell and gene therapy field. You will play a key part in maintaining compliance, supporting quality systems, and contributing to continuous improvement initiatives.

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

Responsibilities:

• Oversee quality assurance for manufacturing operations and related activities.
• Review and approve documents to ensure compliance with Good Manufacturing Practices (GMP).
• Help develop and implement quality policies and procedures.
• Monitor and maintain quality performance metrics.
• Collaborate with other teams to ensure compliance across all operations.
• Review and approve batch records for accuracy and compliance.
• Support facility inspections and assist during audits.
• Conduct internal audits and prepare reports.
• Investigate issues, assess risks, and manage corrective actions.
• Assist with document management and quality system improvements.
• Provide training on GMP and quality systems.
• Offer guidance on quality-related matters to internal teams and external partners.

Key Skills and Requirements:

• A degree in a scientific or technical field (e.g., Chemistry, Life Sciences) is preferred.
• Experience working in a GMP manufacturing environment.
• Familiarity with sterile manufacturing processes is a plus.
• Proficient in using electronic quality management systems (QMS).
• Strong verbal and written communication skills.

For more information, please contact Raif Valery.

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.

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

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