Experience

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  Auxly

  • Canada
  • Consumer Goods
  • 100 - 200 Employee

  • Lead Analytical Scientist

    • Dec 2022 - Present

    As a Lead Analytical Scientist, I specialize in operating and maintaining analytical instruments such as HPLC, LCMS/MS, GC-FID, GC-MS/MS, and ICP-MS. I train and supervise laboratory personnel, perform method validation, and troubleshoot instrument issues. I also manage inventory and ensure equipment is properly calibrated and maintained. With my proficiency in software and computer skills, I automate data processing to increase efficiency. I write and update SOPs and method validation protocols, and collaborate with my team to prioritize tasks in a fast-paced analytical laboratory environment.

  • Analytical Scientist

    • Mar 2019 - Dec 2022

    In a fast-paced, highly cooperative environment in a rapidly expanding industry, I wrote and reviewed SOP documents, assisted in the installation of new, state-of-the-art laboratory equipment, designed test methods on analytical equipment, and ran method validation protocols. I also troubleshooted hardware and software issues on specialized devices in collaboration with vendors, trained new laboratory personnel, and had extensive experience working with analytical systems such as GC-MS, UHPLC, HPLC-MS/MS, ICP-MS, and Prep-HPLC.

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  BioVectra Inc.

  • Prince Edward Island, Canada

  • QC Chemist

    • Feb 2018 - Mar 2019
    • Prince Edward Island, Canada

    As a QC Chemist in a fast-paced, cGMP-compliant laboratory environment, I performed various analyses using advanced instrumentation techniques such as HPLC, GC, UV-Vis, and NMR, as well as bench chemical techniques such as TLC, titrimetry, and gravimetry. I also handled potent and/or cytotoxic compounds, ensuring strict adherence to safety protocols.To maintain accurate records of all laboratory activities, I diligently documented all work in real-time, including completing paperwork for release of materials such as status labels and certificates of analysis. I also played a key role in ensuring optimal performance of analytical instruments, performing regular maintenance and calibration and thoroughly documenting these activities.Overall, my experience as a QC Chemist has equipped me with the technical expertise and attention to detail necessary to thrive in a high-pressure laboratory setting.

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  Delivra Inc.

  • Prince Edward Island, Canada

  • R&D Laboratory Technician

    • Jul 2015 - Jan 2018
    • Prince Edward Island, Canada

    As an R&D Laboratory Technician, I was responsible for designing, performing, and analyzing the results of biological assays, including Western Blot and ELISA. Additionally, I prepared samples for HPLC-MS/MS analysis, conducted chemical synthesis of novel compounds, and utilized mammalian cell cultures for in vitro testing.My work also included preparing various sample types for analysis with bio-assays or HPLC, as well as utilizing both common and specialized computer software. I played a key role in training new laboratory personnel in the use of common equipment and in general laboratory safety procedures.In addition, I helped manage inventory for the laboratory, participated in weekly strategic meetings, and wrote work reports. I also designed and wrote laboratory work instruction documents and Standard Operating Procedures. Lastly, I ensured optimal performance of laboratory equipment by conducting regular calibration and maintenance activities.Overall, my experience as an R&D Laboratory Technician has given me a comprehensive understanding of laboratory operations and enabled me to thrive in a fast-paced, dynamic environment.

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  BD

  • Quebec, Canada

  • Intern in Research and Development

    • May 2013 - Dec 2014
    • Quebec, Canada

    As an intern in R&D at BD Diagnostics, I played an integral role in supporting laboratory operations. I helped manage inventory for research laboratories and calibrated and qualified automated rtPCR equipment. Additionally, I worked in a bio-safety level 3 research environment and prepared and aliquoted solutions.To ensure adherence to rigorous standards, I performed assays following GLP guidelines in a GMP, ISO13485:2003 certified R&D laboratory. Specifically, I conducted rtPCR and gel electrophoresis experiments. I also utilized specialized software to analyze raw data and produce comprehensive work reports.Moreover, I actively participated in weekly strategic meetings to provide updates on project progress and contribute ideas for future research initiatives. Overall, my experience at BD Diagnostics gave me valuable exposure to the day-to-day operations of a leading biotechnology company and equipped me with the skills necessary to excel in a fast-paced, research-driven environment.