Amgen Singapore Manufacturing
biotechnology
AssociateQualityControl(Microbiology)
“Associate Quality Control (Microbiology) at Amgen Singapore Manufacturing. Skills: Quality Control, Microbiology, GMP. Execute testing and/or review for routine environmental, water, raw material and product testing. Sample management such as sample logging, movement, storage”
Industry & Context.
Possess problem solving skills with the ability to apply logic and assess data to troubleshoot and reach decisions or solutions related to assay
Able to support 12-hour rotating day shift (8am - 8pm), inclusive of weekends and public holidays, Fulfilling the medical requirements of this job scope
What They're Looking For.
Must Have
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, 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, 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
Nice to Have
QC laboratory experience preferred
What You'll Do.
Execute testing and/or review for routine environmental
raw material and product testing
Sample management such as sample logging
Involvement in document revisions and report writing
Involvement in method transfers
method validation/verification
Laboratory housekeeping and document archival
Project management / Involvement in QC projects
Support 12-hour rotating day shift
How You'll Work.
Team & Collaboration
Able to interact effectively with variety of communication and working styles; Ability to work well in teams
Process & Methodology
Project management / Involvement in QC projects
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