Oversee and coordinate stability studies and manage stability samples, ensuring compliance with regulatory requirements and project timelines.
Conduct both practical laboratory work and detailed data analysis, including setting up, running, and troubleshooting chromatography instruments such as HPLC.
Take responsibility as a GLP study director for specific projects, managing all aspects from experimental design through to final report writing.
Collaborate closely with a diverse QC team, including principal technical specialists and supervisors, to ensure smooth workflow and technical excellence.
Maintain strict adherence to GLP and GMP standards, ensuring all laboratory activities meet compliance and quality expectations.
Utilize your expertise in analytical techniques, including chromatography, particle size distribution, NMR, and mass spectrometry, to support and enhance laboratory capabilities.
Troubleshoot and resolve analytical issues promptly to maintain project progress and data integrity.
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