CQV ENGINEER

EFOR

Toronto

On-site

CAD 70,000 - 110,000

Full time

10 days ago
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Benefits offered by this job

Professional growth opportunities
Exposure to leading-edge pharma projec
Engaged and supportive team culture

Job summary

EFOR is seeking a CQV Engineer Consultant (Pharma) to join our team on projects in the Greater Toronto Area. This is a fully on-site role in Ontario, Canada, requiring CQV/validation experience and strong collaboration with client teams.

All levels welcome. Degree in engineering or life sciences is preferred, with travel readiness and attention to regulatory compliance. You will write IQ/OQ/PQ protocols and contribute to leading-edge pharma projects within a supportive team.

Qualifications

  • 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.

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

Skills

Effective communication
Problem solving
Travel readiness

Education

Degree in engineering or life sciences

Job description

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:
  • Professional growth opportunities
  • Exposure to leading-edge pharma projects
  • Engaged and supportive team culture
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