Research Scientist​/Principal Research Scientist

Company:
Bio Pharma Services Inc.

Position Title:

Principal Research Scientist
Salary Range: $80,000-$110,000
Job Class:
Full Time

Work Location:

Onsite (North York)

Position Summary:

Under the direction of the Executive Director, Bioanalytical Laboratory Operations, performs special tasks related development of bioanalytical projects of high complexity and using LC-MS/MS.

Duties and Responsibilities:

Performs complex bioanalytical method development and method revision tasks, on LC-MS/MS Instruments.
Expert in method development of small molecules in different biological matrices of animals and humans with different extraction techniques.
Capable of developing method for biologics using LCMS/MS. Which includes, large molecules, ADCs, bispecific compounds, Small peptides and ceramides.
Adjust chromatographic and MS conditions to improve sensitivity, selectivity, peak shape, and robustness.
Subject Matter Expert(SME) for bioanalytical analysis of small molecules LCMSMS analysis.
Evaluate and minimize matrix effects, carryover, interferences, and variability.
Establish and manage internal standards and assess potential co‑medication/endogenous interferences.
Plan and support method validation (accuracy, precision, linearity, selectivity, stability, dilution integrity, etc.).
Document method development, optimization, and validation work clearly in protocols and reports.
Provide technical oversight during routine sample analysis using developed/validated methods.
Review chromatograms and data integration, investigate atypical results, and recommend corrective actions.
Provide technical oversight to R&D chemists (and validation/production chemists) performing method development.
Provides technical training to new chemists and when corrective/preventative action are required in response to technical challenges and failures.
Continually coordinate, organize, and integrate resources used in large complex projects with flexibility to accommodate frequently changing priorities to meet established objectives.
Performs complex bioanalytical method development and method revision tasks, on LC-MS/MS Instruments.
Expert in method development of small molecules in different biological matrices of animals and humans with different extraction techniques.
Capable of developing method for biologics using LCMS/MS. Which includes, large molecules, ADCs, bispecific compounds, Small peptides and ceramides.
Adjust chromatographic and MS conditions to improve sensitivity, selectivity, peak shape, and robustness.
Subject Matter Expert(SME) for bioanalytical analysis of small molecules LCMSMS analysis.
Evaluate and minimize matrix effects, carryover, interferences, and variability.
Establish and manage internal standards and assess potential co‑medication/endogenous interferences.
Plan and support method validation (accuracy, precision, linearity, selectivity, stability, dilution integrity, etc).
Document method development, optimization, and validation work clearly in protocols and reports.
Provide technical oversight during routine sample analysis using developed/validated methods.
Review chromatograms and data integration, investigate atypical results, and recommend corrective actions.
Provide technical oversight to R&D chemists (and validation/production chemists) performing method development.
Provides technical training to new chemists and when corrective/preventative action are required in response to technical challenges and failures.
Continually coordinate, organize, and integrate resources used in large complex projects with flexibility to accommodate frequently changing priorities to meet established objectives.
In addition to General Responsibilities, the following are additional responsibilities regarding the conduct of GLP and Non-GLP studies:
Generates analytical test results in compliance with all current SOPs, protocols, study plans and applicable GLP (OECD), EMA, ICH, FDA and TPD requirements.
Document and communicate any deviations to these instructions directly to the Principal Investigator (for GLP studies) or Study Director (for Non-GLP studies).
Generates method procedures, results, validation, re-validation, and analytical reports…