QA Validation Engineer

As a QA Validation Engineer (Contract), you will be responsible for reviewing and assessing validation documentation across a range of disciplines including Commissioning, Qualification & Validation (CQV), Computer Systems Validation (CSV), Cleaning Validation, Equipment Validation, and Process Validation. This is a fully onsite role (5 days per week), working closely with the QA Validation team. The initial contract is 6 months, Inside IR35 with scope to extend depending on project needs and performance., * Competitive daily rate.

• Opportunity to contribute to high-impact validation projects.
• Work within a collaborative and quality-driven team.
• Potential for contract extension based on performance and business needs.

Strong experience in one or more of the following areas: CSV, Cleaning, Equipment or Process Validation.

• Familiarity with CQV documentation such as SAT, IOQ, and PQ.
• Solid understanding of regulatory frameworks including FDA, EMA, and cGMP.
• Excellent attention to detail and analytical skills.
• Ability to work independently and adapt to shifting project priorities.
• Experience with risk-based validation approaches and document management systems.

You will be joining a leading sterile pharmaceutical manufacturing organisation based in the United Kingdom, recognised for its high standards in quality, compliance, and innovation. The company operates in a dynamic, project-driven environment and is currently expanding its validation team to support new product introductions and ongoing regulatory activities.