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Our client an Indian Biopharmaceutical company is looking for a Labware LIMS who will be responsible for LIMS Implementation, Configuration, Sub-Routine & related query building in Labware LIMS
Key responsibilities of the Role:
• Revision/ modifying tests, specs, sampling plans, templates and other user-managed information, performing new user training and other basic troubleshooting for users
• Creation of master data activity such as building Analysis, Product Specification and Product RDS, Batch link, Batch test template, Sampling point, Test method and Item code
• Importing / Exporting the objective from one server to another server
• Supporting users on Stability module (Creation of Stability Lots, Project & Protocol)
• Resolving online parsing issue (Balance, pH meter, Conductivity meter)
• Resolving File parsing for Empower connected system (HPLC, GC) & PDF parsing issue (Karl Fisher, TOC, FTIR, Potentiometer)
• Supporting users to creation of Lot, Batch, In-Process project, Investigation, Inventory and Standard management in LIMS
• Responsible for implementing and maintaining laboratory instrument interfaces with LIMS and implementing and maintaining statistical Quality Control software interface for charting and data analysis/trending purposes
• Responsible for responding and resolving QC system users inquires and is the technical lead for QC process improvement projects
Note: This is an onsite role from Bangalore location
- Prior experience in reports generation and management of information stored in LIMS for statistical analysis, interpretation of data, and investigating causes
- Good knowledge of LIMS Implementation, Configuration, Sub-Routine & related query building
- Experience of 8-12 years in Pharmaceuticals or BioPharma
Indian Bio Pharmaceutical Company
Pharmaceuticals
8+ years
1
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