Join to apply for the QA Validation Engineer role at Lonza
United States, Tampa (Florida)
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.
Key Responsibilities
- Execute and document validation activities (IQ, OQ, PQ, PPQ), including risk assessments and periodic reviews.
- Support the full Validation Life Cycle—from design through revalidation and continuous improvement.
- Collaborate with internal and external teams to ensure new systems meet cGMP and validation requirements.
- Maintain and update validation-related documentation (SOPs, Change Controls, CAPAs, Deviations).
- Assist in investigations and resolution of deviations involving equipment, systems, and processes.
- Provide validation support during audits and ensure inspection readiness.
Key Qualifications
Bachelor's degree in engineering, life sciences, or related field.2–5 years of validation experience in a GMP-regulated environment.Cross-Functional Communication.Reference : R71162
J-18808-Ljbffr