Assist the Laboratory Operations Manager to manage the infrastructure and support aspects of the Laboratory to ensure that the systems in place are compliant with defined quality requirements.
To ensure that all value stream specific process raw materials, non-routine samples, envops, intermediates and final products are properly analysed and the results recorded in full compliance with current Good Manufacturing Practice (cGMP) and regulatory requirements that meet the defined quality standards.
To ensure that all investigational samples or evaluation samples are analysed and results recorded in full compliance with current Good Manufacturing
Practice (cGMP) and regulatory requirements that meet the defined quality standards.
To ensure all new methods and specifications introduced as part of new product introduction or product lifecycle are validated or verified in compliance with defined quality standards and regulatory requirements.
At least 1-4 years experience in an analytical environment, preferably in the pharmaceutical
GMP and GLP knowledge
Understanding product specification and method of analysis
Knowledge of laboratory instrumentation
Candidates with no prior experience will be considered
We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh| Registration No: R1109239