Clinical Research Associate jobs in Canada

Job summary

A biotechnology company in Greater London is seeking a Scientist I to perform laboratory-based activities supporting lentiviral vector process development. The role includes executing upstream and downstream process studies, performing vector analytics, and generating technical documentation while collaborating with cross-functional teams to support development and regulatory requirements. Ideal candidates should have 2-5 years of experience in biotechnology, especially in cell and gene therapy. A BSc, MSc, or PhD in relevant fields is required.

Qualifications

• Approximately 2 to 5 years’ experience in biotechnology/biological sciences with focus on cell and gene therapy.
• Experience in Upstream Process (USP) operations for vector production.
• Understanding of regulatory filings and associated reports/sections writing.
• Hands-on experience with suspension bioreactors and DSP processes.
• Familiarity with FDA, EMA, GMP, and ICH regulatory requirements.

Responsibilities

• Perform laboratory activities for lentiviral vector (LVV) manufacturing processes.
• Design and execute experiments with guidance, including data analysis.
• Collaborate with cross-functional teams to meet project timelines.
• Author and review development protocols and technical reports.
• Contribute to vector laboratory upkeep and ensure safety standards.