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Labware LIMS
Ref No.: 18-55952
Location: New York City, New York
Position Type:Full Time/Contract
Start Date: 08/06/2018
 Essentials       
•         Hands on experience in Labware LIMS configuration and Static Data Change, Table Master
•         Hands on expertise on LIMS Basic coding and best practices
•         Write performance optimized complex SQL queries and embed into Labware modules
•         Familiarity with instruments and raw data types and parsing using Labstation
•         Design Patterns and Object Oriented development concepts
•         Test Driven Development Frameworks
•         Ability to work with Agile Teams and tools like JIRA, Bitbucket, Confluence etc.
•         Experience of Computerized Systems Validation in cGXP environment, especially GMP
•         Basic understanding of 21 CFR Part 11 and all amendments
•         Basic knowledge of Drug/Consumer/Medical devices research and development life cycle, manufacturing, supply chain
Desirable        
•         Labware v6/v7 certified
•         Agile Scrum certified
•         Design thinking w.r.t Informatics Architecture
•         Inspection/Audit handling from US FDA
•         Continuous Integration and Automated Testing
Responsibilities:
1. Work with IT Leads from customer side and understand requirements, Solution architecture
2. Upgrade v5 modules or system to v6/v7
3. Replace/Refactor v5 codebase using latest methods from v7 Library
4. Build high quality Labware configuration/LIMS Basic custom code, test w.r.t performance and best practices, optimize etc.
5. Work with larger Agile team and integrate build units to meet Epic milestones
6. Support Acceptance tests and release Labware package to Production, execute the scripts
7. Author IQ/OQ/PQ, Integration test scripts and support validation objectives