Job opportunity
Junior Pharmaceutical CQV Consultant
Resolute Workforce Solutions
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 Good 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.
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Apply on source site 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 Good 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.
#J-18808-Ljbffr