Validation / QA Improvement Specialist – Pharmaceutical CV-Library Validation / QA Improvement [...]

Scienceabode; Bolton; On-site; GBP 40,000 - 45,000; Full time

Job summary

A well-established QA function is seeking a Validation / QA Improvement Specialist for a 6-month fixed-term contract in Bolton. The role involves supporting validation activities, developing training, and ensuring compliance with industry standards. Candidates with proven QA validation experience in regulated environments, knowledge of IQ/OQ/PQ, and strong documentation skills are encouraged to apply. The position offers a salary between £40,000 and £45,000 annually, with the potential for contract extension.

Qualifications

• Proven experience in QA validation within a regulated environment.
• Strong working knowledge of IQ/OQ/PQ, equipment validation, and process validation.
• Ability to work independently and manage priorities.

Responsibilities

• Support all validation and ongoing continuous improvement activities.
• Develop and execute validation protocols.
• Ensure compliance with regulatory requirements.

Skills

QA validation experience

Knowledge of IQ/OQ/PQ

Strong documentation skills

Ability to conduct training

Job description

Validation / QA Improvement Specialist (6-Month FTC)

Location: Bolton, site-based

Contract: 6-Month Fixed Term Contract (potential to extend)

Department: Quality Assurance

Job Overview

We are seeking an experienced Validation / QA Improvement Specialist to join our client's QA team on a 6-month fixed term contract. This role will support critical validation activities across equipment, processes, and computerised systems while driving continuous improvement initiatives. The successful candidate will play a key role in ensuring compliance with regulatory and internal quality standards and in supporting the ongoing development of the QA team.

Key Responsibilities

• Support all validation and ongoing continuous improvement activities
• Provide validation and continuous improvement training to the QA team
• Develop and execute validation protocols. Create and carry out tests for equipment, processes, and computer systems to ensure they meet predetermined specifications.
• Conduct equipment and process validation: Perform and document testing for installation, operation, and performance qualification (IQ/OQ/PQ) for new or modified equipment and processes.

Additional Responsibilities

• Ensure validation activities are compliant with regulatory requirements.
• Review and approve validation documentation, protocols, and reports as required.
• Support investigations, deviations, CAPAs, and change control activities related to validated systems.
• Collaborate cross-functionally with Engineering, Manufacturing, IT, and Quality teams to support validation timelines.
• Contribute to the continuous improvement of validation processes, templates, and training materials.

Desired Background

• Proven experience in QA validation within a regulated environment (e.g. pharmaceutical, medical device, biotech, or manufacturing).
• Strong working knowledge of IQ/OQ/PQ, equipment validation, process validation, and computerized system validation.
• Experience developing and executing validation protocols and reports.
• Ability to deliver training and support QA team capability development.
• Strong documentation skills and attention to detail.
• Ability to work independently and manage priorities in a fast-paced environment.

Why Join?

This 6‑month FTC offers an excellent opportunity to contribute to meaningful validation and quality initiatives within a well‑established QA function, while gaining exposure to cross‑functional projects and continuous improvement activities.

£40,000 – £45,000/annum