For International Trade And Development Company
5 - 12 Years
Full Time
Immediate
Up to 40 LPA
1 Position(s)
Bangalore / Bengaluru, Chennai, Coimbatore, Hyderabad, Kochi, Kolkata, Mumbai, Nagpur, Noida, Pune
5 - 12 Years
Full Time
Immediate
Up to 40 LPA
1 Position(s)
Bangalore / Bengaluru, Chennai, Coimbatore, Hyderabad, Kochi, Kolkata, Mumbai, Nagpur, Noida, Pune
Posted By : Rarr Technologies Pvt Ltd
Key Responsibilities:
Design, configure, and implement LabWare LIMS (preferably V6/V7/V8) solutions based on business requirements.
Gather and analyze user requirements for Laboratory Information Management Systems (LIMS) and provide appropriate solutions.
Develop and maintain LIMS applications, including LabWare Basic Language, subroutines, interfacing, upgrade, and validation.
Configure LabWare objects and perform system administration for lab applications as required.
Manage and troubleshoot issues related to LabWare LIMS, including ERP interfaces, label printing software, MDM, and other integrated systems.
Conduct GxP analysis, gap/risk assessment, and ensure compliance with industry standards.
Perform root cause analysis and implement corrective measures for technical issues.
Develop and execute validation protocols for LIMS projects.
Create and customize reports using SAP Crystal Reports.
Provide 24x7 application support and ensure system availability.
Drive process improvements, automation, and impact analysis activities.
Work within SDLC and Agile frameworks; ensure compliance with ITIL and ITSM processes.
Collaborate with cross-functional teams for implementation and support activities.
Required Skills:
Strong conceptual and hands-on experience in LabWare LIMS (V6, V7, V8).
Deep understanding of LabWare architecture and database structures.
Proficient in Oracle PL/SQL and SAP Crystal Reports.
Expertise in LabWare Basic Language, subroutines, and interfacing.
Knowledge and experience in LabWare modules such as:
Stability
Environmental Monitoring (EM)
Inventory & Storage Location Management
Instrument Interfaces
Lot & Sample Management for Clinical Trial and Manufacturing domains.
Experience in LIMS system administration and object configuration.
Strong troubleshooting skills and ability to manage multiple priorities in an unstructured environment.
Understanding of pharma domain, GxP compliance, and risk-based IT application development approaches.
Excellent oral and written communication skills.