Description

You will define, develop, and support GMP e-systems, primarily LabWare LIMS, within manufacturing operations.

This role is on-site.

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.

Key Skills

Education

Not specified