Position Description

QC Specialist (Pharmaceutical/ Contract)
Job Code 15658
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
  • Leads department/ site projects (new QC equipment qualification, QC equipment software upgrade, method validation etc) with minimum guidance
  • Writes required GMP documentations such as SOPs, protocols, reports, deviations, change controls.

 

Requirements

  • Technical background for QC equipment qualification including Computer System Validation (CSV) e.g. window mitigation, empower 3.
  • Competent technical skills in common laboratory techniques (e.g. HPLC, GC, AAS, autotitrator)
  • Technical background for method validation/ transfer.

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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