Job
Description
As a candidate ready to join immediately, you can share your details via email for quick processing. The role requires 4-7 years of experience in Laboratory IT support or CDS administration. You should have hands-on experience with Empower software administration and possess a strong knowledge of chromatography systems and instrument integration. Proven troubleshooting skills for hardware, software, and network connectivity issues are essential. It is important to have a solid understanding of FDA regulations, GxP compliance, and data integrity principles. Previous experience working in regulated environments, specifically Pharma or Life Sciences, is a must. You should be able to collaborate effectively with IT, QA, and laboratory stakeholders, and have exposure to vendor coordination and basic project management activities. Experience in global deployments and multi-site support environments is also required. Key Responsibilities: - Provide Laboratory IT support and CDS administration. - Administer Empower software and ensure its smooth operation. - Troubleshoot hardware, software, and network connectivity issues. - Ensure compliance with FDA regulations, GxP standards, and data integrity principles. - Collaborate with IT, QA, and laboratory stakeholders effectively. - Coordinate with vendors and manage basic project activities. - Support global deployments and provide multi-site support. Qualifications Required: - 4-7 years of experience in Laboratory IT support or CDS administration. - Hands-on experience with Empower software administration. - Strong knowledge of chromatography systems and instrument integration. - Proven troubleshooting skills for hardware, software, and network connectivity issues. - Solid understanding of FDA regulations, GxP compliance, and data integrity principles. - Experience working in regulated environments (Pharma / Life Sciences). - Ability to collaborate effectively with IT, QA, and laboratory stakeholders. - Exposure to vendor coordination and basic project management activities. - Experience in global deployments and multi-site support environments. Good to Have: - Familiarity with NuGenesis or other scientific data management systems. - Knowledge of LIMS or other laboratory systems. - Experience with system validation documentation (CSV lifecycle). - ITIL or service management exposure. As a candidate ready to join immediately, you can share your details via email for quick processing. The role requires 4-7 years of experience in Laboratory IT support or CDS administration. You should have hands-on experience with Empower software administration and possess a strong knowledge of chromatography systems and instrument integration. Proven troubleshooting skills for hardware, software, and network connectivity issues are essential. It is important to have a solid understanding of FDA regulations, GxP compliance, and data integrity principles. Previous experience working in regulated environments, specifically Pharma or Life Sciences, is a must. You should be able to collaborate effectively with IT, QA, and laboratory stakeholders, and have exposure to vendor coordination and basic project management activities. Experience in global deployments and multi-site support environments is also required. Key Responsibilities: - Provide Laboratory IT support and CDS administration. - Administer Empower software and ensure its smooth operation. - Troubleshoot hardware, software, and network connectivity issues. - Ensure compliance with FDA regulations, GxP standards, and data integrity principles. - Collaborate with IT, QA, and laboratory stakeholders effectively. - Coordinate with vendors and manage basic project activities. - Support global deployments and provide multi-site support. Qualifications Required: - 4-7 years of experience in Laboratory IT support or CDS administration. - Hands-on experience with Empower software administration. - Strong knowledge of chromatography systems and instrument integration. - Proven troubleshooting skills for hardware, software, and network connectivity issues. - Solid understanding of FDA regulations, GxP compliance, and data integrity principles. - Experience working in regulated environments (Pharma / Life Sciences). - Ability to collaborate effectively with IT, QA, and laboratory stakeholders. - Exposure to vendor coordination and basic project management activities. - Experience in global deployments and multi-site support environments. Good to Have: - Familiarity with NuGenesis or other scientific data management systems. - Knowledge of LIMS or other laboratory systems. - Experience with system validation documentation (CSV lifecycle). - ITIL or service management exposure.
