Qualifications

• 3-5 years of experience in the pharmaceutical industry.
• PhD or MSc in Chemistry, Biochemistry, Chemical Engineering, or a related field; BSc with relevant experience may be considered.
• Proficient in analytical techniques such as HPLC, Rheometer, Particle Size, and USP Dissolution systems.
• Experience in analytical method development and validation within the pharmaceutical industry.
• Strong data analysis and technical writing skills.
• Ability to manage multiple tasks in a fast-paced environment.
• Familiarity with GMP and knowledge of ICH, FDA, and USP guidelines is a plus.

Responsibilities

• Support analytical development activities including initial lab assessments and method troubleshooting.
• Assist in stability programs through protocol drafting and report writing.
• Prepare and review analytical protocols and reports for validation, development, and stability.
• Conduct data analysis and interpretation to aid development and regulatory activities.
• Coordinate analytical activities with CDMOs and internal teams.
• Assist in the writing and revision of SOPs and manage document lifecycle.
• Contribute to the development of internal technical reports and provide updates on analytical activities.

Benefits

• Onsite position located in Vancouver for hands-on laboratory development work.
• Engagement in diverse analytical development and testing projects for sustained release drug products.
• Opportunity to work closely with cross-functional teams and CDMOs.
• Chance to contribute to impactful pharmaceutical research and development.
• Fostering a culture of continuous learning and technical skill enhancement.