• Own end-to-end delivery of LIMS (CaliberLIMS Preferred) implementation programs ensuring alignment with laboratory operations business goals and regulatory requirements. • Lead requirement gathering solution design and system configuration including workflows and user roles/permissions. • Manage project planning timelines risks & resource allocation to ensure successful and timely delivery. • Drive integration of LIMS with Lab Instrument including Port based File based and CDS (Empower) and enterprise systems (such as SAP and TrackWise) ensuring data integrity and system performance. • Ensure compliance with GxP standards (GMP GLP FDA 21 CFR Part 11) and lead Computer System Validation (CSV) activities. • Act as the primary liaison between business stakeholders IT teams QA and external vendors ensuring clear communication and alignment. • Lead user enablement including training strategy SOP development documentation and change management for successful adoption. • Establish post-go-live support continuous improvement initiatives and system enhancements to optimize performance and user experience.
Job Title: LIMS Implementation & Integration ManagerJob Responsibilities:• Own end-to-end delivery of LIMS (CaliberLIMS Preferred) implementation programs ensuring alignment with laboratory operations business goals and regulatory requirements.• Lead requirement gathering solution design and system ...
• Own end-to-end delivery of LIMS (CaliberLIMS Preferred) implementation programs ensuring alignment with laboratory operations business goals and regulatory requirements. • Lead requirement gathering solution design and system configuration including workflows and user roles/permissions. • Manage project planning timelines risks & resource allocation to ensure successful and timely delivery. • Drive integration of LIMS with Lab Instrument including Port based File based and CDS (Empower) and enterprise systems (such as SAP and TrackWise) ensuring data integrity and system performance. • Ensure compliance with GxP standards (GMP GLP FDA 21 CFR Part 11) and lead Computer System Validation (CSV) activities. • Act as the primary liaison between business stakeholders IT teams QA and external vendors ensuring clear communication and alignment. • Lead user enablement including training strategy SOP development documentation and change management for successful adoption. • Establish post-go-live support continuous improvement initiatives and system enhancements to optimize performance and user experience.