- Applies GMP/GLP in all areas of responsibility, as appropriate
- Demonstrate and promote the company vision
- Regular attendance and punctuality
- Read and understand analytical procedures
- Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs
- Gain a technical understanding of the techniques in which review is being performed
- Use MS Windows applications such as EXCEL, Word, Access, Outlook email
- Conducts all activities in a safe and efficient manner
- Performs other duties as assigned
Master’s degree in a science-related field with 0-2 years of experience in Bio/Pharmaceutical Chemistry drug product/substance testing with knowledge of regulatory requirements.
Theoretical / Practical experience with analytical techniques such as pH meter, Spectroscopy (UV, IR, NMR), Chromatography (HPLC/UPLC, GC, IC…etc.), knowledge of USP/EP compendia, and laboratory software applications such as Waters Empower software, LIMS, Electronic Notebook is preferred.
