- Execute upstream, downstream and/or central services biomanufacturing processes in accordance with approved batch records and SOPs
- Operate bioprocess equipment such as bioreactors, centrifuges, buffer preparation systems, chromatography systems and related manu
- Ensure production activities are completed according to cGMP requirements and production schedules.
Key Responsibilities
Manufacturing Operations
- Execute upstream, downstream and/or central services biomanufacturing processes in accordance with approved batch records and SOPs.
- Operate bioprocess equipment such as bioreactors, centrifuges, buffer preparation systems, chromatography systems and related manufacturing equipment.
- Ensure production activities are completed according to cGMP requirements and production schedules.
Quality & Compliance
- Perform in-process sampling, testing and monitoring of critical quality attributes.
- Maintain accurate and complete GMP documentation, including electronic batch records.
- Adhere to cleanroom requirements, biosafety procedures and EHS regulations.
Equipment & Process Support
- Conduct equipment cleaning, sanitisation and preparation activities.
- Participate in investigations related to manufacturing deviations and support corrective actions.
- Support technology transfer, process validation and continuous improvement initiatives.
Requirements
- Diploma or Degree in Biotechnology, Life Sciences, Biological Sciences, Bioprocess Technology, Chemical Engineering or a related discipline.
- 1 to 4 years of experience in biopharmaceutical, biotechnology, pharmaceutical or manufacturing environments.
- Understanding of GMP and regulated manufacturing environments.
- Experience operating bioprocess equipment is advantageous.
- Comfortable working in a cleanroom environment and following strict compliance procedures.
- Good documentation and communication skills.
Preferred Skills
- Upstream or downstream bioprocessing experience.
- Knowledge of bioreactors, chromatography, filtration or centrifugation systems.
- Experience with electronic batch records (EBR).
- Familiarity with process validation and technology transfer activities.
- Strong attention to detail and problem-solving skills.
We regret to inform that only shortlisted candidates will be notified.
Job Reference: R25150511 Cammy Li Xin Hui
Allegis Group Singapore Pte Ltd, Company Reg No. 200909448N, EA License No. 10C4544
