Job Description

Labware LIMS Developer
Job Number: 20-05240
 
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Labware LIMS Developer for our client in New Brunswick, NJ. 
 
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
 
Position Overview:
  • 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
 
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.
 
Qualifications:
  • 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.
 
If hired, you will enjoy the following Eclaro Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
 
If interested, you may contact:
Maria Castañeda
maria.castaneda@eclaro.com
6463571235
Maria Castañeda | LinkedIn
 
Equal Opportunity Employer:
Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Application Instructions

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