Quality Operations Associate

Talentmark; Hatfield; On-site; GBP 28,000 - 38,000; Full time

Job summary

Talentmark is recruiting for a Quality Operations Associate to join a leading global pharmaceutical organisation on a permanent basis in Hatfield, UK. The role focuses on supporting Quality Systems and ensuring GMP compliance across manufacturing and QA teams.

You will review batch docs, manage deviations and CAPAs, contribute to change control and risk assessments, and help with audits and product transfers. Strong communication and MS Office skills are essential.

Qualifications

• Experience with QA systems and GMP in a pharmaceutical environment.
• Familiarity with deviations, CAPAs, change control, and batch documentation.
• Strong communication and organisational skills; ability to interpret technical information.

Responsibilities

• Support 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.

Skills

Quality Assurance

Quality Systems

GMP

Pharma environment

Tools

MS 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