You will define, develop, and support GMP e-systems, primarily LabWare LIMS, within manufacturing operations.
Responsibilities
Collaborate with Quality, Manufacturing, Supply Chain, Facilities, and Tech Transfer to capture requirements and develop business justifications for new capabilities.
Lead application integration phases by owning User Requirements Specifications, Functional Specifications, Design Specifications, and test cases.
Execute GMP validation activities including IQ/OQ/PQ testing.
Provide technical support and application administration for the laboratory information system.
Required Skills
Bachelor's degree in a technology or relevant scientific discipline.
3+ years of IT or QC experience in life sciences or biopharmaceutical organizations supporting plant-based GMP applications.
Proven expertise implementing and supporting laboratory information systems (LIMS).
Strong understanding of laboratory business processes and the software development lifecycle.
Experience with systems integration.
LabWare LIMS.
T-SQL.
Crystal Reports.
Preferred Skills
LabWare Admin I certification.
Development experience in LabWare LIMS basic.
Experience developing queries and reports using T-SQL or Crystal Reports.