Skip to main content
Post your resume and find your next job on Indeed!

Biomedical Scientist jobs in Ontario

Sort by: -
    • Position Title: Principal Research Scientist.
    • Salary Range: $80,000-$100,000.
    • Work Location: Onsite (North York).
    • View all WELL Health Technologies Corp jobs - Toronto jobs - Research Scientist jobs in Toronto, ON
    • Salary Search: Research Scientist/Principal Research Scientist salaries in Toronto, ON
    • See popular questions & answers about WELL Health Technologies Corp
    • The Laboratory of Behavioural Neuroendocrinology at the Centre for Addiction and Mental Health (CAMH) is seeking a full-time, contract (12 months) Scientific…
    • Job Number: JR105972 Job Title: Biomedical Technologist, Biomedical Engineering Job Category: Paramedical Hospital Location: Centenary Site Job Type: Permanent,…
    • Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Various outside…
    • Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety…
    • For over 50 years, LifeLabs has been Canada’s leading provider of laboratory diagnostic information and digital health connectivity systems, enabling patients…
  • View similar jobs with this employer
    • For over 50 years, LifeLabs has been Canada’s leading provider of laboratory diagnostic information and digital health connectivity systems, enabling patients…
    • Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research…
    • Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research…
    • At KPMG in Canada, our people bring their unique perspectives to Canada’s most important challenges.
    • Here, you can build momentum that reaches beyond our…
    • The University of Ottawa (uOttawa) invites applications for a tenure-track Canada Impact+ Emerging Leader position in Experimental Biophotonics, aligned with…
    • Date Posted (YYYY/MM/DD):
    • Applications must be received BEFORE (YYYY/MM/DD):
    • The University of Ottawa invites applications for a Tier 2 Canada Research Chair (…
    • The Scientific Associate will support scientists and technical staff in the design and execution of studies following established standard operating procedures…
    • Liaising with clinicians, scientists, digital health experts and other collaborators internal and external to CAMH during both proposal development and study…
  • View similar jobs with this employer
    • As a scientist, understand the needs of the project and possible issues, and the vision of the deliverable (report, regulatory dossier, research, risk…
Get email updates for the latest Biomedical Scientist jobs in Ontario

By creating a job alert, you agree to our Terms . You can change your consent settings at any time by unsubscribing or as detailed in our terms.

Career Resources:

Research Scientist/Principal Research Scientist
WELL Health Technologies Corp
·
2.4
4000 Weston Road, Toronto, ON M9L 3A2
$80,000–$100,000 a year
Full-time
Apply now

Job details

Here’s how the job details align with your profile.

Pay

$80,000–$100,000 a year

Job type

Full-time

Full job description

Company: BioPharma Services Inc.
Position Title: Principal Research Scientist
Salary Range: $80,000-$100,000
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.

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 for direct submission to regulatory authorities.
  • Records raw data promptly and accurately and in compliance with the OECD Principles of Good Laboratory Practice.
  • Works in a safe manner, complying with all relevant safety procedures.
  • Exercises health precautions to minimize risk to him/herself and to ensure the integrity of the study. Communicates to the Laboratory Management for any relevant known health or medical condition so he/she can be excluded from operations that may affect the study.

Qualifications:

  • MSc or Ph.D. in Analytical chemistry or in a related field, with a minimum of 5 years of related experience directly involved in the advanced-level use and applications of LC-MS/MS. Or
  • BSc. /College Diploma in Analytical Chemistry or a related field with a minimum of 10 years of related experience directly involved in the advanced-level use and applications of LC-MS/MS.
Let Employers Find YouUpload Your Resume