to join our team on projects in the Greater Toronto Area. Key Responsibilities:
Carry out commissioning, qualification, and validation activities Write and execute protocols (IQ/OQ/PQ) and ensure regulatory compliance Collaborate closely with client and project teams Support troubleshooting and documentation What We’re Looking For:
Degree in engineering, life sciences, or related field CQV/validation experience in pharma or biotech (all seniorities considered) Strong communication and problem-solving skills Adaptable, proactive, and detail-oriented Available to travel and work fully on site at client locations What We Offer:
Skilled growth opportunities Exposure to leading-edge pharma projects Engaged and supportive team culture
📌 CQV ENGINEER (Winnipeg)
🏢 EFOR
📍 Winnipeg
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.