Quality Operations Associate

Talentmark; United Kingdom; On-site; GBP 28,000 - 42,000; Full time

Job summary

ROYAL SOCIETY OF CHEMISTRY is seeking a Quality Operations Associate for a permanent role within a leading global pharmaceutical environment. You will support GMP-aligned quality systems, review batch records and drive continuous improvement in collaboration with manufacturing and QC teams.

The role focuses on deviations, CAPAs, Change Control, audits and product transfers, ensuring robust quality across manufacturing and packaging. Strong communication and problem-solving skills are essential.

Qualifications

• Knowledge of Quality Assurance, Quality Systems and GMP within a pharmaceutical environment.
• Understanding of pharmaceutical manufacturing and packaging processes.
• Experience or exposure to deviations, CAPAs, Change Control or batch documentation.
• Strong communication, problem-solving and organisational skills.
• Confident using Microsoft Office and interpreting technical information.

Responsibilities

• Support the implementation and maintenance of Quality Systems in line with GMP and corporate standards.
• Review and approve batch documentation and quality-related records.
• Manage deviations, CAPAs, Change Control and risk assessments.
• Support audits, inspections, validation, product transfers and new product introductions.
• Collaborate with manufacturing, QC and other departments to maintain product quality.

Skills

Quality Assurance

GMP Compliance

Quality Systems

Communication

Organisational skills

Tools

Microsoft Office

Job description

Talentmark is recruiting for a Quality Operations Associate to join a leading global pharmaceutical organisation on a permanent basis.

The Role

• Support the implementation and maintenance of Quality Systems in line with GMP and corporate standards.
• Review and approve batch documentation, manufacturing records and quality-related documents.
• Manage quality processes including deviations, CAPAs, Change Control and risk assessments.
• Support audits, inspections, validation, product transfers and new product introductions.
• Work closely with manufacturing, QC and other departments to maintain product quality and drive continuous improvement.

Your Background

• Knowledge of Quality Assurance, Quality Systems and GMP within a pharmaceutical environment.
• Understanding of pharmaceutical manufacturing and packaging processes.
• Experience or exposure to deviations, CAPAs, Change Control or batch documentation.
• Strong communication, problem-solving and organisational skills.
• Confident using Microsoft Office and interpreting technical information.

The Company

Our client is a leading global pharmaceutical organisation committed to developing and delivering high-quality medicines.

Applicants must have the right to work in the UK.