Develop and optimize manufacturing processes for biotechnology products, ensuring scalability and efficiency.
Operate and maintain bioreactors, fermenters, and other specialized equipment used in the manufacturing process.
Conduct quality control tests and assessments to ensure compliance with regulatory standards and product specifications.
Collaborate with cross-functional teams, including research and development, to implement process improvements and drive innovation.
Maintain accurate documentation and records of manufacturing processes, ensuring traceability and adherence to regulatory guidelines.
Stay updated with industry trends and advancements in manufacturing technologies and implement best practices accordingly.
Scop of the work:
Perform activities in GXP environment. Activities including but not limited to, manufacturing operations, Commissioning & Qualification activities, any other activities as instructed by the supervisor.
To perform and execute GXP operations independently and in accordance with Site safety standards
To support manufacturing activities by performing verification of Automation or MES recipes
Lead and drive manufacturing improvement initiates
Perform update of Standard Operating Procedures and Training Procedures
Requirements:
Min 2 years of working experience required in similar role.
Experience in the pharmaceutical industry would be an added advantage.
Strong knowledge of bioprocessing techniques, including fermentation, purification, and downstream processing.
Proficiency in operating and troubleshooting bioreactors, centrifuges, chromatography systems, and other related equipment.
Familiarity with quality control procedures and regulatory compliance in the biotechnology sector, particularly in Singapore.
Excellent problem-solving skills and ability to work independently and in a team-oriented environment.