QA Validation Engineer - Contract Role (Sterile Pharma, Swindon - Onsite)
Have you got what it takes to succeed The following information should be read carefully by all candidates.
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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