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- Employment type
- Full-time
- Experience level
- Mid-level · 2+ years
- Minimum education
- Bachelor’s degree
- Posting language
- English
- Working hours
- 40 hours per week
- Seniority
- Not Applicable
- Application method
- Apply on LinkedIn (LinkedIn sign-in required)
Job summary
Carry out commissioning, qualification, and validation activities, including writing and executing IQ/OQ/PQ protocols while ensuring regulatory compliance. Collaborate with client and project teams to support troubleshooting and documentation.
Job details
CQV Engineer Consultant (Pharma) – All Levels – Fully On Site – Ontario, Canada About US : EFOR is an ambitious consultancy with over 3,000 consultants, specializing in the life sciences sector. 🚀 About the Role: We are looking for CQV (Commissioning, Qualification & Validation) Engineer Consultants (all levels welcome) 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: Training 📚 Professional growth opportunities 📈 Exposure to leading-edge pharma projects Engaged and supportive team culture 🤗 Interested? Or know someone who might be? 😊 We’re happy to receive your application or your referrals! If you know talented validation engineers who would be a great fit, please invite them to reach out, too! 😊
What you’ll do
Carry out commissioning, qualification, and validation activities, including writing and executing IQ/OQ/PQ protocols while ensuring regulatory compliance. Collaborate with client and project teams to support troubleshooting and documentation.
Requirements
A degree in engineering, life sciences, or a related field is requested, along with CQV or validation experience in the pharmaceutical or biotechnology industry; all seniority levels are considered. Candidates should have strong communication and problem-solving skills, be adaptable, proactive, and detail-oriented, and be available to travel and work fully on site at client locations.
Benefits
- Training
- Professional Growth Opportunities
- Exposure To Leading-Edge Pharmaceutical Projects
- Supportive Team Culture
Listed skills
- Validation · Preferred
- Problem solving · Preferred
- adaptability · Preferred
- Regulatory Compliance · Preferred
- Attention to detail · Preferred
- Documentation · Preferred
- Communication · Preferred
- Troubleshooting · Preferred
Other relevant skills
Identified from the job description. Confirm important requirements above.
- Commissioning
- Qualification
- Validation
- Protocol Writing
- Protocol Execution
- IQ/OQ/PQ
- Regulatory Compliance
- Troubleshooting
- Documentation
- Communication
- Problem-Solving
- Adaptability
- Proactivity
- Attention To Detail
Job areas
- Engineering
- Consulting
- Manufacturing
- Science & Research