QA Validation Engineer

4 weeks ago

London, United Kingdom Hays Full time

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 To be successful in this role, you will need: 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 If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.TPBN1_UKTJ

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