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ALTEN Canada

C&Q Project Manager (Pharmaceutical)

Toronto, ON, Canada
North York, ON, Canada

Pay: The current target salary range for this role is $90,000 – $105,000 per year.
Job type: Full-time
Apply by: Oct 25, 2026
Experience: 5+ years of experience in pharmaceutical, biotechnology, or other regulated GMP manufacturing environments.
Posting language: English
Posted: Sep 25, 2026

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Original job description

About ALTEN:

In just three decades, ALTEN has become a global leader in Research & Development, Engineering, IT Services, Life Sciences, and Network Services. With a presence in more than 30 countries and a team of over 60,000 employees, we are trusted by industry leaders worldwide to deliver pioneering solutions and drive technical excellence.

ALTEN CANADA, a proud subsidiary of ALTEN headquartered in France, is dedicated to serving the Canadian market. With offices in Montreal and Toronto, we combine global expertise with local insight to accelerate innovation across Canada.

At ALTEN CANADA, our consultants thrive on solving complex, highly technical challenges across diverse industries. From Life Sciences to Energy, Automation to Manufacturing, Aviation, Defense. Automotive, Rail and Transportation to Information Systems and Telecommunications, our unwavering commitment to excellence shaping the future of technology and industry.

Job Description:

Develop, maintain, and manage the overall C&Q schedule for the project, ensuring all activities are planned, prioritized, and executed according to project timelines.
Coordinate daily with the C&Q team, engineering, quality, validation, and project stakeholders to align upcoming activities, resource requirements, and project deliverables.
Monitor the execution of C&Q activities and provide oversight to ensure work is progressing according to approved scope, schedule, and project objectives.
Identify schedule conflicts, execution challenges, and project risks, and proactively drive resolution plans to minimize impact on project milestones.
Serve as the primary escalation point for C&Q-related issues, facilitating timely decision-making and engaging the appropriate stakeholders when required.
Track project progress, maintain status reports, and communicate schedule performance, risks, and key updates to the project leadership team.
Ensure C&Q activities are completed in accordance with GMP requirements, commissioning and qualification principles, and established project procedures, while not directly performing execution work.

Requirements:

5+ years of experience in pharmaceutical, biotechnology, or other regulated GMP manufacturing environments.
Demonstrated experience coordinating, planning, scheduling, or managing Commissioning & Qualification (C&Q), Validation, Capital Projects, or Engineering projects.
Strong understanding of C&Q lifecycle activities, including commissioning, IQ, OQ, PQ, and associated project execution phases.
Proven ability to manage project schedules, resolve issues, assess risks, coordinate cross-functional teams, and communicate effectively with technical and business stakeholders.

Why Join Us?

ALTEN Canada fosters a dynamic, collaborative work environment where every team member is empowered to reach their full potential. We are deeply committed to investing in our people by offering meaningful experiences and supporting continuous learning, growth, and career development

As part of our dedication to employee well-being, we provide a competitive and comprehensive benefits package that includes:

Collective insurance and group retirement savings plans
4 weeks of vacation starting from year one
Corporate discounts and team-building activities
Tailored professional development plans

At ALTEN Canada, your skills are celebrated, your ambitions supported, and your growth continuously nurtured. Join us and discover the difference of working with a company that values innovation, collaboration, and excellence, where endless possibilities await.

ALTEN CANADA is committed to promoting diversity, equity, and inclusion. We strive to provide a work environment where every individual feels welcomed, valued, and respected, allowing them to thrive to their full potential. This includes our dedication to offer accessibility measures to those who require them. Should you require any accommodation during our recruitment process, please reach out to us.

Alten uses artificial intelligence tools to support certain administrative aspects of the recruitment process, such as interview note-taking and résumé formatting. These tools do not make hiring decisions. Candidate consent is always obtained prior to use.

In accordance with our compensation practices, ALTEN is providing the salary range associated with this opportunity. Final compensation will be determined after considering several factors, including professional experience, skill set, educational background, certifications, and geographic market conditions. The current target salary range for this role is $90,000 – $105,000 per year.

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More about this job

Responsibilities

Manage and maintain the project’s C&Q schedule, coordinate daily with technical and project stakeholders, and monitor execution against approved scope, timelines, and objectives. Identify and resolve schedule conflicts and risks, escalate C&Q issues, report progress to project leadership, and ensure activities comply with GMP and project procedures without performing execution work directly.

Requirements

Requires at least five years of experience in pharmaceutical, biotechnology, or another regulated GMP manufacturing environment, with demonstrated coordination or management of C&Q, validation, capital, or engineering projects. Candidates should understand the C&Q lifecycle, including commissioning, IQ, OQ, and PQ, and be able to manage schedules, risks, issues, cross-functional teams, and stakeholder communications.

Skills

Commissioning And Qualification
Project Scheduling
Project Management
Validation
GMP Compliance
Risk Assessment
Issue Resolution
Cross-Functional Coordination
Stakeholder Communication
Project Reporting
Commissioning
Installation Qualification
Operational Qualification
Performance Qualification
Capital Projects
Engineering Project Coordination

Benefits

Collective Insurance
Group Retirement Savings Plan
Four Weeks Of Vacation Starting From Year One
Corporate Discounts
Team-Building Activities
Tailored Professional Development Plans

Visa sponsorship

Not detected in the job text

Keywords

Pharmaceutical
Biotechnology
GMP
Commissioning And Qualification
C&Q
Validation
Capital Projects
Engineering Projects
Commissioning
Installation Qualification
Operational Qualification
Performance Qualification
Project Scheduling
Project Execution
Risk Management
Issue Resolution
Cross-Functional Coordination
Stakeholder Communication
Project Status Reporting
Project Procedures

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