Draft, compile, review and update appropriate laboratory documents such as analytical methods and specifications, method validation/equivalency protocols/reports, local procedures and guidelines relating to GMP and operational framework of the laboratory
Based in Singapore, the regional hub for Asia Pacific (AP) and top-ranked biopharmaceutical company on the Straits Times and Statista’s list of Best Employers in Singapore for two consecutive years (2020, 2021).
To perform QC testing of raw materials, incoming goods, intermediates, and/or finished products under cGMP conditions for QC release or as part of stability studies.
Perform laboratory testing on samples, including Base, Sediment and Water (BSW), ash content, water by distillation, flash point, sediment by extraction, density and viscosity.
We are seeking a Production Chemist to provide technical and process support for Active Pharmaceutical Ingredient (API) manufacturing. The role will support safe, compliant and efficient production through process troubleshooting, optimisation, validation and continuous improvement.
Collaborate with laboratory analyst to contribute towards achieving the objectives of the department. Provide technical training on laboratory instrumentation to laboratory analysts.
Collaborate with laboratory analyst to contribute towards achieving the objectives of the department. Provide technical training on laboratory instrumentation to laboratory analysts.
Draft, compile, review and update appropriate laboratory documents such as analytical methods and specifications, method validation/equivalency protocols/reports, local procedures and guidelines relating to GMP and operational framework of the laboratory