CSV Engineer

About The Job CSV EngineerLocation: Edmonton, Alberta (onsite role) Client Industry: Pharmaceutical Manufacturing PharmEng Technology is seeking an experienced Computer System Validation (CSV) Specialist for a 12-month on-site consulting engagement with our client in Edmonton, Alberta. This role is essential in supporting GMP compliance for critical laboratory systems and software in a sterile manufacturing environment. Key Responsibilities

• Develop and execute validation protocols (URS, FS, IQ, OQ)
• Qualify laboratory and manufacturing equipment (e.g., sterile filling lines, HVAC, HPLC)
• Perform CSV activities in compliance with cGMP and regulatory standards
• Provide hands-on, on-site support and coordination with cross-functional teams
• Maintain documentation, manage deviations, and support audit readiness

Qualifications

• Proven experience in IT Qualification and CSV within GMP-regulated environments
• Strong documentation and validation protocol development skills
• Effective communication and stakeholder coordination capabilities
• Ability to work full-time on-site in Edmonton

About PharmEng Technology PharmEng Technology is a full-service consulting firm providing expert compliance and validation services to the pharmaceutical, biotechnology, and medical device industries. We pride ourselves on delivering high-quality solutions through industry expertise and collaborative client partnerships. If you're a validation professional looking for your next consulting opportunity, we'd like to hear from you.