Position Description

QC Administrator (Pharmaceutical/ 6 months contract)
Job Code 15703
Division GMP TECHNOLOGIES (S) PTE LTD (EA Licence:11C3793)
Job Placement Location Singapore
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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

  • University degree in a relevant science discipline
  • Or 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)

 

To apply, please visit to www.gmprecruit.com

To find out more about this opportunity, please contact Lionel Liew at lionel.liew@gmprecruit.com.

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd   |   EA Licence: 11C3793 |   EA Personnel: Lionel Liew   |   Registration No: R1330693

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