QA Validation & Compliance Associate

Value Apothecaries; United Kingdom; On-site; GBP 42,000 - 70,000; Full time

Job summary

Cencora is seeking a QA/Validation professional in the UK to support GDP and GMP compliance. You will develop and maintain the Validation Master Plan, create validation protocols, and ensure documentation quality across QA activities.

You will participate in client and regulatory audits and maintain up-to-date regulatory knowledge. Responsibilities include maintaining sVMP, handling change controls, and reporting KPIs while ensuring timely corrective actions and archival of QA records.

Qualifications

• Ideally educated to A-level or equivalent.
• Ideally 3 years' experience working in a validation role within a GDP or GMP environment.
• Understanding of GDP and GMP regulations.
• Understanding of ISO 9001.
• Ability to maintain knowledge of applicable regulatory and quality requirements.

Responsibilities

• Develop and maintain the site Validation Master Plan (sVMP).
• Develop validation and qualification protocols and perform validation activities per the sVMP.
• Perform qualification/validation for quality-critical assets per change controls.
• Maintain accurate records of qualification, validation and QA activities.
• Support ongoing GDP, GMP, ISO 9001 compliance and client requirements.
• Review daily/monthly temperature trends and participate in audits.

Skills

Attention to detail

Regulatory compliance

Documentation skills

Quality assurance

Effective communication

Education

A-level or equivalent

GDP/GMP knowledge (training)

Job description

Cencora is seeking a QA/Validation professional in the UK to support GDP and GMP compliance. You will develop and maintain the Validation Master Plan, create validation protocols, and ensure documentation quality across QA activities.

You will participate in client and regulatory audits and maintain up-to-date regulatory knowledge. Responsibilities include maintaining sVMP, handling change controls, and reporting KPIs while ensuring timely corrective actions and archival of QA records.