Build pharmaceutical CQV expertise as a Junior Consultant with Brevitas in Richmond Hill, supporting regulated facilities, equipment, and systems. Work across client sites, hybrid assignments, or the Richmond Hill office.

Resolute’s recruitment division is hiring for Brevitas, where you will support project execution alongside experienced consultants. Rotate through commissioning, qualification, validation, computer system validation, project coordination, and technical writing. Develop technical capabilities while contributing to project delivery in regulated life sciences environments.

Key Responsibilities:

- Support project planning, coordination, and execution across project lifecycles
- Execute CQV protocols and follow up on documented deviations
- Prepare technical protocols, reports, procedures, and project deliverables




- Apply engineering principles, industry standards, and Valuable Manufacturing Practices
- Develop digital tools, automated workflows, templates, and dashboards

Requirements:

- Bachelor’s degree in engineering or a related discipline
- One to three years of relevant engineering or validation experience
- Pharmaceutical, biotechnology, life sciences, or regulated manufacturing experience
- Familiarity with Microsoft Office and project management tools
- Legal entitlement to work in Canada

Bring engineering knowledge, attention to detail, and communication skills to pharmaceutical CQV projects across the Greater Toronto Area.

📌 Junior Pharmaceutical CQV Consultant (Canada)
🏢 Resolute Workforce Solutions
📍 Canada