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Associate Quality Control (Microbiology)

Singapore, Singapore · Job Posted May 29, 2026
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Job Description

Associate Quality Control (Microbiology) Amgen Singapore Manufacturing HOW MIGHT YOU DEFY IMAGINATION? Amgen is one of the world’s leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics, but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring an Associate Quality Control (Microbiology) in Amgen Singapore Manufacturing.

Job Responsibility

  • Execute testing and/or review for routine environmental, water, raw material and product testing (e.g. bioburden, endotoxin, qPCR, microbial ID etc.)
  • media, reagent and culture qualification (e.g. growth promotion, DNA positive controls, microorganisms culture types etc.)
  • Sample management such as sample logging, movement, storage of samples, reconciliation of sample receipt, aliquoting samples, management of stability samples, and sample shipment to Amgen network sites and/or contract labs
  • Involvement in document revisions and report writing
  • Involvement in method transfers, method validation/verification and sample type qualification
  • Laboratory housekeeping and document archival
  • Project management / Involvement in QC projects (e.g. Continuous Improvement/ Operational Excellence)
  • When required, able to support 12-hour rotating day shift (8am - 8pm), inclusive of weekends and public holidays
  • All listed tasks and responsibilities are deemed as essential functions to this position
  • however, business conditions may require reasonable accommodation for additional tasks and responsibilities

Requirements

  • Bachelor’s Degree in Microbiology, Biological Sciences, Life Sciences or related technological field and 2 years of directly related experience
  • Associate’s Degree in Microbiology, Biological Sciences, Life Sciences or related technological field and 4 years of directly related experience
  • Diploma in Microbiology, Biological Sciences, Life Sciences or related technological field / GED and 6 years of directly related experience
  • Have at least 1-3 years of relevant professional work experience within the biopharmaceutical industry and QC laboratory experience preferred
  • Possess sound knowledge and understanding of GMP pharmaceutical operations and associated QC testing methods, inclusive of GMP laboratory operation
  • Experience with Quality Control testing and laboratory operations for common microbial testing methods and equipment (e.g. including but not limited to bioburden, endotoxin, microbial identification, environmental monitoring, microbial limits, growth promotion, biological indicators)
  • Able to interact effectively with variety of communication and working styles and ability to work well in teams
  • Ability to manage multiple simultaneous activities in a rapidly changing environment
  • Possess problem solving skills with the ability to apply logic and assess data to troubleshoot and reach decisions or solutions related to assay

What we offer

  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

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Associate Quality Control (Microbiology)

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Amgen is one of the world’s leading independent biotechnology companies. For ove...
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Singapore , Singapore
Salary
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Requirements
Requirements
  • Bachelor’s Degree in Microbiology, Biological Sciences, Life Sciences or related technological field and 2 years of directly related experience
  • Associate’s Degree in Microbiology, Biological Sciences, Life Sciences or related technological field and 4 years of directly related experience
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  • Experience with Quality Control testing and laboratory operations for common microbial testing methods and equipment (e.g. including but not limited to bioburden, endotoxin, microbial identification, environmental monitoring, microbial limits, growth promotion, biological indicators)
  • Able to interact effectively with variety of communication and working styles and ability to work well in teams
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  • Possess problem solving skills with the ability to apply logic and assess data to troubleshoot and reach decisions or solutions related to assay
  • Your selection for this role will be subject to fulfilling the medical requirements of this job scope
Job Responsibility
Job Responsibility
  • Execute testing and/or review for routine environmental, water, raw material and product testing (e.g. bioburden, endotoxin, qPCR, microbial ID etc.)
  • media, reagent and culture qualification (e.g. growth promotion, DNA positive controls, microorganisms culture types etc.)
  • Sample management such as sample logging, movement, storage of samples, reconciliation of sample receipt, aliquoting samples, management of stability samples, and sample shipment to Amgen network sites and/or contract labs
  • Involvement in document revisions and report writing
  • Involvement in method transfers, method validation/verification and sample type qualification
  • Laboratory housekeeping and document archival
  • Project management / Involvement in QC projects (e.g. Continuous Improvement/ Operational Excellence)
  • When required, able to support 12-hour rotating day shift (8am - 8pm), inclusive of weekends and public holidays
What we offer
What we offer
  • Vast opportunities to learn and move up and across our global organization
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  • High school/GED + 4 years of Quality experience OR Associate's + 2 years of Quality experience OR Bachelor's degree and 6 months of Quality, Microbiology or Operations experience
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  • Perform microbial assessments and other GMP documentation as required (reports, assessments, SOP revisions)
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