Lonza is seeking a Computer Systems Validation Engineer to ensure GxP computerized systems used in biopharmaceutical development and manufacturing meet regulatory and quality requirements. You will plan and execute CSV activities across the system lifecycle, including risk assessments, requirements, test protocols, and reports in alignment with FDA, EU, and data integrity guidelines. Partnering with QA, IT, and manufacturing, you will troubleshoot issues, support audits, and drive continuous improvement while working with advanced technologies in a highly collaborative, science-driven environment.
...Purpose To perform daily processing of accounts payable transactions, ensuring that invoices are processed and paid in an accurate and timely manner. Principal Responsibilities Match invoices to purchase receipts. Enter data from invoices to our accounting...
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Job Title: Data AnalystJob Category: Information TechnologyTime Type: Full timeMinimum Clearance Required to Start: NoneEmployee Type... ...portfolio.Responsibilities:Stakeholder Engagement & Evidence Collection:Conduct structured interviews, facilitated sessions, and questionnaires...
...Systems quality improvement functions through the analysis of data and indicators. Responsible for identifying and monitoring ongoing... .... Assists in the development of process metrics, data collection tools and presentations of resultant data throughout the Health...
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