Responsible for sampling and laboratory testing on raw materials, packaging materials, in-process, and final products for compliance to quality standard.
Responsible for in-process line check, environmental monitoring, and water monitoring programs.
Support laboratory operations, including sample receipt, sample subdivision and labelling, waste disposal, stability sample packing etc.
Perform documentation in accordance to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements.
Conduct training to fellow colleagues on simple procedures (E.g., hygiene and safety).
Practice laboratory good housekeeping and ensure laboratory safety procedures are followed.
Highlight abnormality during testing and obtain authorization for laboratory investigation from supervisor.
Perform equipment troubleshooting where required.
Other responsibilities include laboratory equipment calibration/maintenance, equipment qualification, method development and validation as well as involvement in improvement projects.
Requirements:
Diploma and above
Fluency in English, both oral and written
Ability to work autonomously and under pressure with a strong analytical mindset.
Proficient in MS Office and in-depth knowledge of preventive measures and laboratory best practices
Good leadership skills to delegate tasks to assistant lab analysts
Experience in laboratory equipment operations such as GC, HPLC, UVS, and FTIR etc. with good troubleshooting knowledge preferred.
Minimum 1 or 2 years of laboratory experience in pharmaceutical/related industry.
For senior position, minimum 3 years QC experience in pharmaceutical/related industry is required.