Laboratory Analyst

Job Summary

• Perform the regulated analysis of drugs and metabolites contained in biological samples (bioanalytical extraction methods – SPE, LL, PP) for production studies and for certain validation parameters using LC-MS/MS, in accordance with good laboratory practices (GLP), the regulations of the United States Food and Drug Administration (21 CFR Part 58) and the principles of the OECD.
• Read applicable procedures.
• Complete adequately the documentation related to the work performed, including redaction of deviation and information sheet.
• Analyze chromatograms using software.
• Perform other related tasks as required.

• University degree in biochemistry, chemistry or any other related field (B.Sc. or M.Sc.)
• Advanced written and spoken English (bilingualism preferred)
• At least 1 year of experience in a similar position or any relevant experience in the pharmaceutical industry (knowledge of GLP is an asset)
• Knowledge of Microsoft Office, ThermoFisher Scientific Watson LIMS and Sciex Analyst software
• Ability to work independently and prioritize tasks
• Ability to work efficiently and in an organized manner to ensure projects are completed on time
• Flexibility and adaptation to different types of projects
• Ability to create a good working relationship
• Team work
• Have a positive, proactive attitude and be motivated