QC Associate (LIMS System Support)

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Manpower Singapore
Southwest
SGD 60,000 - 80,000
Be among the first applicants.
2 days ago
Job description

QC Associate (LIMS System Support)
15-Months Contract
Industry: Pharmaceutical
Location: Tuas
Salary up to $6500 depending on experience

Job Summary:

  • Subject Matter Expert for Laboratory Information Management System (Labware LIMS)

Responsibilities:

  • Responsible for LIMS master data configuration for integration with SAP S4 HANA.
  • Responsible for configuration of master data for QC laboratory instrument Preventative Maintenance (PM) / Calibration (CAL) Work order in SAP.
  • Authors cross-functional qualification documents e.g. Risk assessment, User acceptance testing (UAT) and Qualification Summary report and conduct UAT testing in validation environment and release to production.
  • Execute laboratory changes such as Labware LIMS updates and test method changes.
  • Handle change/enhancement request, working closely with Global LIMS team to improve existing workflow in LIMS.
  • Provide guidance, coaching and training to the team for laboratory change in LIMS.
  • Support initiatives for continuous improvement in QC processes related to Lot (Raw Materials, IPC, FP) management, Standard and reagent inventory, Environmental Monitoring, Stability program and QC Instrument/ Equipment PM /CAL management in LIMS/ SAP system with QC system team.
  • Authors and/or revise SOP, protocols and reports.
  • Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and Data integrity requirements.
  • Support and backup of QC system projects/activities, including laboratory asset lifecycle management, Continuous periodic verification of analytical method and stability program.
  • Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records related to these tasks.
  • Any other duties as assigned by line manager.

Requirements:

  • 3 years of experience in quality control within the pharmaceutical industry, including knowledge of Good Manufacturing Practices (GMP) and regulatory requirements.
  • Bachelor's or Master's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology.
  • Diploma in Applied Chemistry, Chemical & Pharmaceutical Technology, Pharmacy Science or related and 6+ years of relevant experience in the biotechnology or pharmaceutical industry.
  • Advanced knowledge and experience in Labware LIMS.
  • Advanced knowledge and experience in SAP S4 HANA.
  • Process-oriented thinking and knowledge in integrating Laboratory software with SAP ERP module.
  • Knowledge of regulations and standards of the pharmaceutical industry, Global Quality policies and Data Integrity Requirements.
  • Knowledge of the quality systems and associated technologies.
  • Good understanding of good laboratory practices, good documentation practice and data integrity requirements.

Contact:
Lim Pey Chyi - apple.lim@manpower.com.sg
Recruitment Consultant (R2090579)
Manpower Staffing Services (S) Pte Ltd
EA Licence: 02C3423

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