Summary from listing
The Senior Validation Engineer leads and oversees customer and site validation activities for sterilisation processes, ensuring compliance with regulatory, quality, and customer requirements. The role manages complex validation projects, coordinates validation cycles and documentation, supports internal and external audits, commissions and recommissions sterilisation chambers, provides training and mentoring, and acts as a technical and operational delegate for the Regional Senior Validation Manager. A bachelor's degree in Chemistry or Chemical Engineering and 3–5 years of validation or senior engineering experience in an ISO 11135 and ISO 13485-compliant medical device or regulated manufacturing environment are required.
