Pharmaceutical CQV Engineer

MANTU GROUP SA; Toronto; On-site; CAD 60,000 - 80,000; Full time

Job summary

A leading technology consulting firm in Toronto is seeking experienced CQV Engineers to contribute to critical pharmaceutical projects. The role includes leading commissioning activities, preparing CQV documentation, and ensuring compliance with regulatory standards. Candidates should have a Bachelor’s degree in Engineering or Life Sciences and proven CQV experience in the pharmaceutical sector. Join a diverse international team focused on growth and development in a fast-paced environment.

Benefits

Strong training system

Dynamic work environment with internal events

International community with diverse backgrounds

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or a related field.
• Proven experience in CQV within pharmaceutical or biotech manufacturing environments.
• Strong knowledge of GMP regulations and industry standards.

Responsibilities

• Lead and execute commissioning, qualification, and validation (CQV) activities for pharmaceutical projects.
• Prepare and review CQV documentation including protocols and reports.
• Ensure compliance with GMP and other global regulatory standards.

Skills

CQV experience

Problem-solving skills

Analytical skills

Education

Bachelor’s degree in Engineering or Life Sciences

Tools

GMP regulations knowledge

Experience with HVAC and bioreactors

Job description

Overview

Are you an experienced CQV professional looking to contribute to critical pharmaceutical projects? We are currently seeking CQV Engineers to join our growing team in Toronto! If you\'re open to exciting new opportunities and thrive in fast-paced, highly regulated environments, we’d love to hear from you.

Responsibilities

• Lead and execute commissioning, qualification, and validation (CQV) activities for pharmaceutical equipment, utilities, and systems.
• Prepare and review CQV documentation, including protocols (IQ/OQ/PQ), reports, and risk assessments.
• Ensure compliance with GMP, FDA, EMA, and other global regulatory standards.
• Collaborate with cross-functional teams including QA, Engineering, Manufacturing, and Project Management.
• Troubleshoot systems and support investigations for deviations and non-conformances.
• Participate in FAT/SAT execution and system handover processes.

Requirements

• Bachelor’s degree in Engineering, Life Sciences, or a related field.
• Proven experience in CQV within pharmaceutical or biotech manufacturing environments.
• Strong knowledge of GMP regulations and industry standards (ISPE, ASTM E2500, etc.).
• Experience with equipment and systems such as clean utilities, HVAC, autoclaves, lyophilizers, and bioreactors.
• Excellent documentation, problem-solving, and analytical skills.
• Ability to work independently and collaboratively in a highly regulated environment.

Why choose us

• An international community bringing together more than 110 different nationalities.
• An environment where trust is central: 70% of our leaders started their careers at the entry level.
• A strong training system with our internal Academy and more than 250 modules available.
• A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.).

Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

Who are we?

Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering. We’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success.