Senior Technical Lead

HCL America, Inc.
United States
7 days ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Compensation
$98,000.0 - $151,000.0
Working hours
Regular working hours
Job source

Tech stack

Microsoft Word Microsoft Excel Microsoft Windows Active Directory Macintosh Computers Software Applications Data Integrity System Testing Iq/oq/pq Extreme Programming GXP Servicenow

Job description

This position is responsible for supporting IT related functions as applicable to Analytical Instruments per Baxter Quality System procedures.

Under moderate oversight by senior team member or manager, the incumbent will:

  • Support IT related activities for all laboratory systems including Atomic Absorption, Gas Chromatographs, Liquid Chromatographs, Mass Specs, Electron Microscopes, NMR’s, Engineering and Infuscale systems.

  • Apply knowledge or quickly learn cGXPs, relevant SOP curriculum, routine project procedures, project management, and other training as appropriate.
  • Serve as IT project lead with projects of intermediate scope and cross-functional teams.
  • Set up and install/upgrade new PC’s when needed for lab equipment
  • Support IT functions for the qualification of new equipment,

coordinate system change control requests and re-qualification activities, as well as manage systems retirements and periodic reviews.

  • Support all labs in Round Lake including Techl, Tech2, DDEL, WG,

and the Penicillin building that contain Validated Systems.

  • Support Active Directory and Data Integrity project.
  • Perform System Administrator duties for Agilent OpenLab ECM and Xybion Compliance Builder.
  • Monitor the Service Now Help Desk ticketing system for any App related issues.
  • Perfoms IT related technical reviews of validation package deliverables.
  • Support all Windows Operating Systems, including XP, Windows 7, 8, and 10.
  • Support Macintosh as well as PC based systems.
  • Management and archival of all software and/or hardware for approved package documents.
  • Handle routine tasks timely, accurately.

Requirements

  • Solid understanding of IT functions related to the instrument qualification process.
  • Direct or indirect industry knowledge.
  • Ability to communicate effectively at all levels in verbal and written form, including technical/business writing.
  • Excellent organizational skills.

Ability to work independently or in teams, Proficient in Computer Software and hardware, Microsoft Word and Excel Must have excellent organizational, oral and written communication skills.

Must Have Skill

Computer System Validation (CSV),IT Support Monitoring,OpenLab ECM,Life-Sciences (GxP/FDA/CSV/IQ/OQ/PQ)

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