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Analytical Development Scientist

Job in Vancouver, BC, Canada
Listing for: Eupraxia Pharmaceuticals Inc.
Full Time position
Listed on 2026-06-04
Job specializations:
  • Research/Development
    Research Scientist, Clinical Research, Medical Science, Data Scientist
Salary/Wage Range or Industry Benchmark: 107000 - 140000 CAD Yearly CAD 107000.00 140000.00 YEAR
Job Description & How to Apply Below

Job Description Role Summary

Analytical Development Scientist is responsible for supporting technical operations related to analytical development and testing of sustained release drug products (polymer drug delivery systems). This includes analytical development, stability studies, data analysis, and documentation to support ongoing and new programs. This is an onsite position in Vancouver, and the scientist is required to perform laboratory development work.

Reports to:

Associate Director, Analytical Chemistry.

Key Responsibilities
  • Support analytical development activities including initial lab assessments, method development, and troubleshooting
  • Support stability programs including protocol drafting, report writing, and data trending
  • Prepare and review analytical protocols and reports (validation, development, stability)
  • Perform data analysis and interpretation to support development and regulatory activities
  • Support coordination of analytical activities with CDMOs and internal teams
  • Assist with SOP writing, revisions, and document lifecycle management
  • Contribute to internal technical reports
  • Routinely provide updates on analytical activities
Requirements
  • 3–5 years experience in pharmaceutical industry
  • PhD or MSc in Chemistry, Biochemistry, Chemical Engineering, or related field. Candidates with BSc plus relevant work experience will be considered
  • Experience with analytical techniques such as HPLC (RP, SEC), Rheometer, Particle Size, USP Dissolution systems, thermal analysis, etc.
  • Experience with analytical method development and validation in pharmaceutical industry
  • Strong data analysis and technical writing skills
  • Ability to manage multiple tasks in a fast-paced environment
  • Familiarity with GMP and basic knowledge of ICH, FDA, and USP guidelines is an asset
Additional Attributes
  • Highly self motivated
  • Ability to work independently and as part of a team
  • Detail oriented and organized
  • Accountable and proactive
  • Strong communication skills
  • A continuous learning mindset

Salary Range: $107,000 to $140,000 depending on education and relevant experience. Within the posted range, individual pay is determined by job related skills, relevant experience, education and/or training. Please note that the range details above reflect base pay only. A bonus will be available based on performance and remaining in post for the agreed contract duration. We also offer a competitive benefits package.

This is an opportunity to work in a small, entrepreneurial, and highly motivating environment, with strong exposure to analytical development and regulatory activities.

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Position Requirements
5+ Years work experience
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