Analytical Development Scientist

Eupraxia Pharmaceuticals

$107K — $140K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 3-5 years of experience in the pharmaceutical industry
  • PhD or MSc in Chemistry, Biochemistry, Chemical Engineering, or related field; BSc with relevant experience accepted
  • Familiar with analytical techniques like HPLC, Rheometer, and USP Dissolution systems
  • Proficient in analytical method development and validation
  • Strong data analysis and technical writing skills
  • Effective multitasking in a fast-paced environment
  • Basic knowledge of GMP, ICH, FDA, and USP guidelines preferred

Responsibilities

  • Support analytical development activities and troubleshoot methods
  • Assist in drafting stability study protocols and reports
  • Prepare and review validation and stability analytical protocols
  • Analyze data to support development and regulatory submissions
  • Coordinate analytical activities with CDMOs and internal teams
  • Facilitate SOP writing and document management
  • Contribute to internal technical reports and provide updates on activities

Benefits

  • Competitive benefits package including performance bonus
  • Opportunity to work in a small, entrepreneurial environment
  • Strong exposure to analytical development and regulatory activities
Full Job Description
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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