Power BI

Author and maintain validation documentation, including: Validation Plans Traceability Matrices Test Scripts and Protocols Validation Reports Support change control activities, system upgrades, releases, and decommissioning efforts. Develop and maintain SOPs, work instructions, and system administration documentation. Serve as a system administrator for assigned laboratory informatics platforms. Partner with laboratory users and management to gather business requirements and translate them into system solutions. Lead or support implementation of new laboratory systems and enhancements. Monitor system performance, identify opportunities for optimization, and recommend process improvements. Collaborate with global stakeholders, vendors, and subject matter experts on system functionality and strategy. Provide end-user support, troubleshooting, training, and documentation as required. Ensure systems remain compliant with applicable regulatory and quality standards., Power BI Chemistry Visionary Management Innovation Informatics Life Sciences Biotechnology Change Control Pharmaceuticals Medical Devices Computer Science Process Improvement Information Systems Traceability Matrix Business Requirements System Administration

Chemistry Visionary Management Innovation Informatics Life Sciences Biotechnology Change Control Pharmaceuticals Medical Devices Computer Science Process Improvement Information Systems Traceability Matrix Business Requirements System Administration Computer System Validation Engineering Design Process Verbal Communication Skills Good Manufacturing Practices End-User Training And Support Good Laboratory Practice (GLP), validation, change control, decomission, CRO, LIMS, Power BI, smartsheet, Bachelor’s Degree in Biology, Chemistry, Life Sciences, Computer Science, Information Systems, or related technical field. 3+ years of experience supporting laboratory systems, scientific software, or computer system validation. Experience working within regulated pharmaceutical, biotechnology, CRO, or medical device environments. Knowledge of GLP, GxP, GMP, and computer system validation principles. Experience with change control, documentation management, and software lifecycle practices. Strong written and verbal communication skills. Ability to manage multiple priorities in a fast-paced environment., Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors., Engineering Design Process Verbal Communication Skills Good Manufacturing Practices End-User Training And Support Good Laboratory Practice (GLP) Software Development Life Cycle Troubleshooting (Problem Solving) Laboratory Information Management Systems

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