Your new company

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.

Your new role

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 fully onsite role offers an initial 3 to 6-month contract, with potential for extension depending on project scope and performance.

What you'll need to succeed

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

What you'll get in return

• 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.

What you need to do now