Position Description

QC Administrator (LES or LIMS) – Till Dec 2020 (Global Pharma MNC, West)
Job Code 15707
Division GMP TECHNOLOGIES (S) PTE LTD (EA Licence:11C3793)
Job Placement Location Singapore
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  • Global Pharma MNC
  • Work location: Tuas
  • Company Transport Pick up available

 

Responsibilities:

  • Have previous working experience in cGMP laboratory environment
  • Supports the Laboratory Execution System (LES) system in QC
  • Load and configure test method templates in LES system
  • Coordinates and performs lifecycle management of LES test method templates/master data in LES system.
  • Execute System Acceptance Test Protocols (SATPs) related to LES as required.
  • Provides support on LES-related matters which includes the hypercare period after new test method roll-out in LES system.
  • Writes required GMP documentations such as SOPs, protocols, reports, deviations, change controls
  • Knowledge is transferred effectively to routine testing team e.g. training

 

Requirements:

  • Fresh graduate with University degree in a relevant science discipline can be considered
  • Minimum Diploma with at least 4 years of relevant working experience
  • Strong technical ability with IT tools, management of databases used in regulated environment IT tools (such as Excel, SAP, LIMS, ELN)
  • Meticulous, proactive, autonomous 
  • Highly organized and able to manage multiple tasks

 

To apply, please visit to www.gmprecruit.com and search for Job Reference:15707

To find out more about this opportunity, please contact Alexandra Calingo at: alexandra@gmprecruit.com

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Alexandra Calingo | Registration No: R1101491

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