Job Details

  • Title: Labware LIMS Developer
  • Code: RCI-31980-1
  • Location: New Brunswick New Jersey (NJ) 08903
  • Posted Date: 06/17/2020
  • Duration: 6 Months
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  Job Description

  • The candidate will serve a key role in supporting Labware LIMS V7 to develop and configure customized software product/system to meet client requirements as well as supporting static data building.
  • May include end-to-end software development starting from analysis moving on to design, implementation, QA, delivery and maintenance.
  • Applies knowledge of technologies, applications, methods, processes and tools to support a client, project or entity.
  • Under moderate supervision from more senior developers the candidate will assume the following responsibilities:

Key Responsibilities:

  • Support creation of static data to support Biologics Development and Small Molecule Business users under stringent timelines.
  • Configure and customize LIMS as per business requirements.
  • Perform basic or complex configuration of LIMS.
  • Extensive experience working with LIMS Basic to develop complex customize solutions.
  • Support integration of scientific and nonscientific applications with LIMS.
  • Ability to translate business requirements to technical documentation and artifacts.
  • Must be able to wireframe and prototype solutions.
  • Help project team with the design and development tasks
  • Provide Tier 2/3 support in resolving help desk tickets in timely fashion.
  • Work multiple projects simultaneously.
  • Strong understanding of Software Development Lifecycle; experience with all phases of a SDLC.
  • Ability to interact with users and translate needs into maintainable configurations, extensions and customizations.
  • Ability to design, author, edit and execute test scripts in Microfocus tool.

Key Competencies:

  • 8+ Years in information management working on large projects.
  • 5+ Years’ experience working in Pharmaceutical industry.
  • Experience in building interfaces to Biovia-ELN systems, WATERS-EMPOWER and SAP is a plus.
  • Strong background with Oracle & SQL Databases is desired.
  • Strong working experience in Database Programming using RDBMS databases like Oracle & SQL Server is a plus.
  • Experience working with QA tools such as ALM for creating test scripts.
  • Knowledge of building Windows Applications using .Net Development is desired but not required.
  • Knowledge of cGXP and 21CFR Part11 standards and strong knowledge of laboratory and process operations in Pharmaceutical Development.
  • LIMS Admin 1 certification is a plus.

Additional requirements below:

  • SDLC - 3+ years
  • .NET - 1-3 years
  • Pharma- 1+ years
  • SQL - 1+ years
  • GXP - 1+ years