Join PharmEng Technology as a CQV Engineer based in Toronto, Ontario, and lead critical commissioning and qualification projects. Apply your expertise to enhance design and execution.
PharmEng Technology seeks an experienced CQV Engineer to support various technical services related to commissioning and qualification. You will independently perform validation tasks while collaborating with management to optimize throughput. This role offers exposure to diverse projects, including equipment qualification and system validation efforts across the pharmaceutical sector.
Key Responsibilities:
• Provide direct services for commissioning and qualification activities
• Review documentation for compliance with regulations




• Assist in user requirements and functional specs development
• Participate actively in all validation phases
• Troubleshoot and resolve validation deviations
Requirements:
• Bachelor's degree in engineering, biology, or related field
• 2 to 5 years of CQV experience in life sciences
• Expertise in facilities and utilities validation
• Strong knowledge of cGMP guidelines
• Proven ability to manage complex validation tasks
Utilize your talents to advance PharmEng’s cutting-edge solutions and patient-centric goals in healthcare.
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📌 CQV Engineer Role in Toronto
🏢 PharmEng Nordic ApS
📍 Toronto