CQV Engineer Consultant - Pharma Focus
Job Description & How to Apply Below
At EFOR, you will be an integral part of the team, working on various Commissioning, Qualification, and Validation projects in the Greater Toronto Area. Ideal candidates will possess a degree in engineering or a related discipline and relevant CQV experience in the pharmaceutical or biotech industries. Strong communication and an adaptive approach are essential for success in this role.
Key Responsibilities:
• Execute commissioning, qualification, and validation initiatives
• Write and manage IQ/OQ/PQ documentation
• Support regulatory compliance efforts
• Collaborate with clients and team members
• Troubleshoot issues and maintain documentation
Requirements:
• Engineering or life sciences degree
• Experience in CQV or validation in pharma
• Excellent communication and analytical skills
• Proactive, detail-focused attitude
• Availability for travel and on-site work
Grow your professional expertise at EFOR by contributing to vital pharma projects!
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