QA Validation Engineer - Contract Role (Sterile Pharma, Swindon - Onsite)
Your new company
A leading pharmaceutical organisation specialising in sterile manufacturing is seeking a skilled QA Validation Engineer to support a high-impact project. With a strong commitment to quality and regulatory compliance, this company offers a dynamic and collaborative environment for experienced contractors.
Your new role
As a QA Validation Engineer, you will serve as a Document Reviewer for Commissioning, Qualification, and Validation (CQV) activities. You'll be responsible for reviewing technical documentation related to equipment used in sterile pharmaceutical manufacturing, ensuring alignment with cGMP, FDA, and EMA standards. You'll collaborate with cross-functional teams to identify gaps, recommend corrective actions, and support continuous improvement efforts.
What you'll need to succeed
* Extensive experience in CQV within sterile pharmaceutical manufacturing
* Strong knowledge of FDA, EMA, and cGMP regulations
* Exceptional attention to detail and analytical skills
* Proficiency in document management systems and quality management software
* Excellent communication skills and the ability to work independently
* Familiarity with risk-based validation approaches
What you'll get in return
* A 3-to 6-month contract with potential for extension
* Opportunity to work onsite in Swindon with a reputable pharmaceutical company
* A chance to contribute to critical quality assurance processes in a regulated environment
* Competitive daily rate and a supportive project team
What you need to do now
If you're an experienced QA professional ready to take on a new challenge in sterile pharma, apply now or get in touch to learn more about this exciting opportunity.
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