Work Schedule: This position will initially work a regular Monday to Friday schedule, from 8:00 a.m. to 5:15 p.m. As the business grows, the role may transition to a 12-hour rotating shift schedule covering both day and night shifts. Candidates should be comfortable with and open to supporting shift operations in the future if required.
Work Authorization: For this opportunity, we are currently unable to provide employment visa sponsorship. We welcome applications from candidates who are authorized to work in Singapore without employer sponsorship.
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Perform quality control microbiological testing of raw materials, incoming goods, intermediates, and/or finished products under cGMP conditions for QC release or as part of stability studies.
Participate in method transfer, verification, and validation for new product introductions.
Conduct monitoring for facility’s utilities systems.
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Perform quality control microbiological testing of raw materials, incoming goods, intermediates, and/or finished products under cGMP conditions for QC release or as part of stability studies.
Participate in method transfer, verification, and validation for new product introductions.
Conduct monitoring for facility’s utilities systems.
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Performs, reviews, and interprets complex, esoteric, and routine chemical, hematological, coagulation, renal, lipid, and hormonal analyses by manual, automated, and/or microscopic means.
Integrates analytical results with specific and highly varied clinical trial protocols to evaluate credibility, appropriateness and accuracy of test results in order to facilitate entry or exclusion of subjects from research programs.
Operates, maintains, troubleshoots and repairs clinical laboratory equipment, including routine preventative maintenance, calibrations, and safety checks.
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