The Analyst is responsible for performing the laboratory work on pre-clinical and clinical validation studies and sample analysis studies for dose formulation/inhalation samples. They will ensure the integrity of all Analytical data with respect to GLPs and appropriate regulatory requirements.
• Working to GLPs, SOPs, and current industry best practices.
• Operation of HPLC-UV, fluoresence, ELSD instruments.
• Operation of GC-MS and GC-TCD instruments is an asset.
• Analysis, documentation, data interpretation, and summary of results.
• Respond to QA comments
• Assist in the daily operational tasks of the laboratory.
• Any other related tasks as assigned.
• Experience and knowledge of analytical instrumentation.
• A strong team player with excellent oral and written communication skills.
• Skilled in data interpretation and contributing to report writing.
• Excellent interpersonal skills.
• Functional English is required, Bilingual: English and French is an asset.
Start date: ASAP
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