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Added 12 mins ago
SS
Unregulated Care Provider
Sienna Senior Living
Simcoe Lodge, ON · Simcoe, ON
- Part-time
…compassionate, high-quality care that supports residents’ health, safety, and overall well-being. As an individual and part of a wider team, you will be a strong contributor to the culture…
Added 12 mins ago
SS
Unregulated Care Provider
Sienna Senior Living
Simcoe Lodge, ON · Simcoe, ON
- Part-time
…compassionate, high-quality care that supports residents’ health, safety, and overall well-being. As an individual and part of a wider team, you will be a strong contributor to the culture…
Added 12 mins ago
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(CAN) Associé de jour, rénovation
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Added 12 mins ago
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ALTEN Canada

Pharmaceutical Facility Project Manager/Engineer

Mississauga, ON, Canada

$90,000 to $95,000 CAD / year · Full-time

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Job details

Pay: $90,000 to $95,000 CAD / year
Job type: Full-time
Apply by: Nov 25, 2026
Posting language: English
Posted: Oct 26, 2026

Original job description

About ALTEN:

In just three decades, ALTEN has emerged as a global leader in Research and Development, Engineering, Information Technology Services, Life Sciences, and Network Services. Our footprint spans across 30 countries, with over 60,000 consultants driving innovation and technical excellence. Trusted by industry giants, we have become synonymous with pioneering solutions and unwavering expertise.

ALTEN CANADA, a proud subsidiary of ALTEN headquartered in France, is committed to serving the Canadian market. With local offices in Montreal and Toronto, we bring our global expertise to the forefront of Canadian innovation.

At ALTEN CANADA, our consultants thrive on tackling complex and highly technical projects across a diverse range of industries. From Manufacturing to Information Systems, IT Automation to Life Sciences, Energy to Automotive, Rail and Transportation to Telecommunications, Aerospace and Defense, our commitment to excellence knows no bounds.

About the Role

We are seeking a detail-oriented and proactive Facilities Engineer/ Pharmaceutical Construction PM with strong project management experience in a GMP-regulated environment. In this role, you will oversee facility expansion projects from planning through execution, ensuring compliance with Good Manufacturing Practices (GMP) and other regulatory requirements. You will coordinate with contractors, vendors, and internal teams to ensure timelines, budgets, and quality standards are met.

Key Responsibilities

Project Oversight: Regularly review project scope, timelines, and milestones to ensure expansion projects remain on track.
Stakeholder Coordination: Liaise with construction teams, architects, equipment suppliers, and other stakeholders to ensure project specifications are met.
Schedule Management: Align all trades (construction, electrical, HVAC, etc.) on timelines, manage task dependencies, and mitigate potential delays.
Budget Monitoring: Track and manage project budgets, ensuring expenses remain within approved limits.
GMP Compliance: Ensure all design and construction activities meet GMP standards and regulatory requirements (Health Canada, FDA).
Inspections & Audits: Coordinate internal audits and support external regulatory inspections.
Documentation Management: Maintain detailed project documentation (design specs, validation reports, as-built drawings) to ensure traceability and compliance.
Site Walkthroughs: Conduct regular site inspections to verify progress, quality, and adherence to safety standards.
Engineering Design Review: Evaluate and approve technical designs (HVAC systems, cleanroom layouts, water/waste systems) to ensure compliance and operational efficiency.
Equipment Integration: Coordinate the integration of pharmaceutical equipment (e.g., autoclaves, filtration systems, reactors) into facility layouts.

Required Qualifications

5+ years in a GMP-regulated environment as a Facilities Engineer, or in building systems oversight/project management related to GMP facilities (pharmaceutical preferred; medical device, food & beverage, or cosmetics accepted).
Project management or coordination experience with projects valued at $100k+ (managing projects between $200k–$2M).
Skills:
Strong communication and interpersonal skills, with the ability to work effectively across multiple vendors and contractors.
Proven ability to manage budgets, schedules, and cross-functional teams.

Nice to Have

Experience with pharmaceutical cleanroom design and validation processes.
PMP certification or equivalent project management training.

Why Join Us?

ALTEN Canada fosters a dynamic and collaborative work environment where team members are empowered to unleash their full potential. We believe in investing in our talent, offering stimulating experiences, and supporting professional growth and development at every turn.

As part of our commitment to our team members, we offer a comprehensive benefits package including

Collective Insurance & RRSP
Corporate Discounts
4 weeks of vacation
Numerous corporate activities.
Personalized professional development plans

Join ALTEN Canada and embark on a journey of endless possibilities, where your talents are celebrated, and your ambitions are nurtured. Experience the difference of working with a company that values innovation, collaboration, and excellence in every endeavor.

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.

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More about this job

Responsibilities

Oversee pharmaceutical facility expansion projects from planning through execution, managing scope, schedules, budgets, contractors, vendors, and internal stakeholders. Ensure GMP and regulatory compliance through design reviews, site inspections, audits, documentation, and integration of pharmaceutical equipment.

Requirements

Requires at least five years of experience in a GMP-regulated environment, preferably in pharmaceutical facilities, and project management or coordination experience with projects valued at $100,000 or more. Candidates should be able to manage budgets, schedules, vendors, contractors, and cross-functional teams; cleanroom design and validation experience and PMP certification or equivalent training are preferred.

Skills

Project Management
GMP Compliance
Facilities Engineering
Pharmaceutical Construction
Budget Management
Schedule Management
Stakeholder Coordination
Contractor And Vendor Coordination
Regulatory Compliance
Audit And Inspection Coordination
Project Documentation
Engineering Design Review
Cleanroom Design
Equipment Integration
HVAC Systems
Cross-Functional Teamwork

Benefits

Collective Insurance
RRSP
Corporate Discounts
Four Weeks Of Vacation
Corporate Activities

Visa sponsorship

Not detected in the job text

Keywords

Good Manufacturing Practices
GMP
Health Canada
FDA
Pharmaceutical Manufacturing
Facility Expansion
Facilities Engineering
Project Scope
Project Milestones
Budget Monitoring
Schedule Management
Contractor Coordination
Vendor Coordination
Regulatory Inspections
Internal Audits
Project Documentation
Validation Reports
As-Built Drawings
Site Inspections
HVAC Systems
Cleanroom Design
Water And Waste Systems
Autoclaves
Filtration Systems
Reactors
Equipment Integration
PMP Certification
Medical Devices
Food And Beverage

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