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Reference # : 17-00894 Title : Sr. Lab System Engineer
Location : New Brunswick, NJ
Position Type : Contract
Experience Level : Start Date : 06/19/2017  
Description
SR. LAB SYSTEM ENGINEER
NEW BRUNSWICK, NJ

Project Description:

Manages the day to day operations and support of the scientific applications such as:
  • Biovia/Accelrys/VelQuest SmartLab/LES,
  • Biovia/Accelrys/VelQuest CIMS, Inventory Management (Biovia-Lims), Biovia/Accelrys/Symyx eLN (electronic laboratory notebook)
  • Waters Empower 3 Chromatography Data System.
  • Performs system administration, support, user account setup, and maintenance activities for scientific systems.
  • Assists with projects relating to laboratory software implementation, upgrades, and support.
  • Applies project management methods and tools effectively.
  • Participates on project teams as technical subject matter expert for key projects.
  • Works with end users and/or business capability managers to understand, verify and develop requirements for laboratory systems or enhancements.
  • Interprets business goals and requirements and devises technical solutions.
  • Acts as a liaison between the business and IT service providers in order to coordinate enhancements, provide integration, and resolve issues.

Required Skills:
  • Bachelors in computer science, chemistry, biology or information technology with equivalent experience in a scientific discipline.
  • At least 3-5 years of experience and hands on work with the support or implementation of software systems preferably in a scientific GXP environment.
  • Experience managing software projects and integrating third party COTS software is preferred.
  • Experience developing or modifying VelQuest/LES procedures using Method Builder, parsing routines, and instrument readings.
  • Experience developing or modifying Pipeline Pilot protocols.
  • Experience developing or modifying CIMS/Biovia-LIMS consumables templates and workflows.
  • Experience with HPQC or HP-ALM for test script execution is preferred.
  • Experience with computer system validation in a regulated GxP environment is required.
  • The successful candidate will be expected to quickly develop a detailed understanding of the role of pharmaceutical development and will be expected to provide effective liaison with infrastructure and IT support groups.
  • Excellent multidisciplinary teamwork and strong communications skills are essential.
  • Must work effectively with minimal oversight and proactively seek feedback from management.





This 6+ month position starts ASAP.

Please E-MAIL your resume (attachment to email) with rate and availability to Dannielle: danni@alphaconsulting.com

ALPHA'S REQUIREMENT #17-00894
W2 ONLY