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1y Biotechnologist (Up to 6k, West) #HFT

External
RECRUIT EXPRESS PTE LTD logoRecruit Express · Ngee Ann City, Singapore
S$48K–S$72K/yrContractUnknown1w ago
ComplianceDocumentationProcess ImprovementSAP
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Requirements

  • Dip/Deg in any relevant discipline with minimally 3 years of experience
  • Experience in a GMP biologics manufacturing environment.
  • Hands-on experience in either: Upstream (cell culture/bioreactors),Downstream (chromatography/TFF/purification), or Central Services (media/buffer prep, dispensing, autoclaves).
  • Ability to work permanent rotating 12-hour shifts.
  • For interested candidates, please submit your latest resume to jacquelinefong@recruitexpress.com.sg
  • Jacqueline Fong Hsin Ting (R21103226)
  • Recruit Express Pte Ltd
  • Company Reg. No. 199601303W
  • EA License Number: 99C4599

Additional Information

1. Biologics Manufacturing Operations Execute manufacturing activities in a cGMP-compliant biologics production facility. Follow batch records, SOPs, and production schedules. Perform equipment setup, operation, monitoring, and cleaning. Complete production documentation accurately and on time. 2. Process Operations (Depending on Assigned Area) Upstream Manufacturing Cell culture operations from vial thaw to large-scale bioreactor production. Media and buffer preparation. Sampling and monitoring of cell growth and process parameters. Downstream Manufacturing Protein purification using chromatography systems. Tangential Flow Filtration (TFF), viral filtration, and bulk filling. Monitoring purification performance and product quality. Central Services Buffer and media preparation. Raw material sampling, weighing, and dispensing. Operation of autoclaves, glass washers, and other support equipment. 3. Equipment & Systems Monitoring Use manufacturing systems such as LIMS, SAP, and automated process control systems. Monitor process data and respond to alarms or process deviations. Support troubleshooting activities during production. 4. Quality & Compliance Ensure compliance with GMP, EHS, and regulatory requirements. Review batch records and logbooks. Participate in deviation investigations and CAPA activities. Support internal and external audits. 5. Continuous Improvement & Team Support Identify process improvement opportunities. Participate in commissioning, validation, and technology transfer activities. Work closely with QA, QC, Engineering, Maintenance, and Manufacturing Science & Technology teams. May mentor junior biotechnologists and assist shift supervisors when required


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