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Added 2 days ago
R
Analyst II, QC Microbiology (18-month Fixed-Term Contract)
Resilience
Mississauga, ON · CAN - ON - Mississauga - Meadowpine Blvd
- Full-time
…filling operations to verify adherence to aseptic technique, and lead the creation and assessment of environmental monitoring and utilities trending reports, identifying and escalating…
Added 5 days ago
B
Validation Specialist
Belcan
Montreal, QC · Greater Montreal Metropolitan Area
- Contract
Réviser les dessins d’ingénierie, les documents de conception et les dossiers de qualification afin d’assurer la conformité aux exigences GMP.
Added 9 days ago
TF
Validation Engineering Specialist II – Equipment Engineering
Thermo Fisher Scientific
Mississauga, ON
- Full-time
Lead equipment commissioning and qualification activities and support project manager.
Added 9 days ago
WS
Corporate Compliance, Supplier Quality & Regulatory Affairs Engineer
Wolf Steel Ltd
Barrie, ON
- Full-time
Work in conjunction with the organization's regulatory compliance program, and lead from an integrated management systems perspective to ensure adherence to applicable laws, standards,…
Added 10 days ago
N
Corporate Compliance, Supplier Quality & Regulatory Affairs Engineer
Napoleon
Barrie, ON
- $82,400 to $113,300 CAD / year
- Full-time
Work in conjunction with the organization's regulatory compliance program, and lead from an integrated management systems perspective to ensure adherence to applicable laws, standards,…
Added 10 days ago
N
Corporate Compliance, Supplier Quality & Regulatory Affairs Engineer
Napoleon
Barrie, ON
- Full-time
Work in conjunction with the organization's regulatory compliance program, and lead from an integrated management systems perspective to ensure adherence to applicable laws, standards,…
Added 11 days ago
LS
Senior Director / Site Quality Head - Canada
Lock Search Group
Toronto, ON · Greater Toronto Area, Canada
- Full-time
…of operational excellence and Good Manufacturing Practice (GMP)…
Added 13 days ago
C
Design Project Manager
CRB
Mississauga, ON
- $122,000 to $160,000 CAD / year
- Full-time
The Design Project Manager will lead multidisciplinary design teams in delivering innovative, compliant, and efficient facility solutions for clients in the life sciences, biotechnology,…
Added 13 days ago
C
Design Project Manager
CRB
Mississauga, ON
- $122,000 to $160,000 CAD / year
- Full-time
The Design Project Manager will lead multidisciplinary design teams in delivering innovative, compliant, and efficient facility solutions for clients in the life sciences, biotechnology,…
Added 27 days ago
E
Quality Assurance Manager - Eurofins ExperNorth, Inc.
Eurofins
Vaughan, ON
- $80,000 CAD / year
- Full-time
Strong Project Manager: You excel at managing multiple priorities in a fast-paced environment. You effectively organize resources, manage timelines, and see tasks through from start to…
Added 27 days ago
Directeur, Ingénierie du site - Director, Site Engineering
GRIFOLS, S.A.
Montreal, QC
…d’ingénierie du site, de maintenance, des installations, des utilités GMP et non GMP, de l’étalonnage, de la fiabilité ainsi que de l’exécution des projets d’investissement (CAPEX). Ce…
Added 27 days ago
Directeur, Ingénierie du site - Director, Site Engineering
GRIFOLS, S.A.
Montreal, QC
…d’ingénierie du site, de maintenance, des installations, des utilités GMP et non GMP, de l’étalonnage, de la fiabilité ainsi que de l’exécution des projets d’investissement (CAPEX). Ce…
Added 27 days ago
E
Quality Assurance Manager - Eurofins ExperNorth, Inc.
Eurofins
Vaughan, ON
- Up to $80,000 CAD / year
- Full-time
Strong Project Manager: You excel at managing multiple priorities in a fast-paced environment. You effectively organize resources, manage timelines, and see tasks through from start to…
Added 1 month ago
Ingénieur/Spécialiste en Validation - Validation Engineer / Specialist 1
GRIFOLS, S.A.
Montreal, QC
Added 2 months ago
TP
Senior Director / Site Quality Head - Canada
Teva Pharmaceuticals
Whitchurch-Stouffville, ON
- Full-time
…of operational excellence and Good Manufacturing Practice (GMP)…
Added 1 month ago
AT
Microbiology Superintendent
Agilent Technologies
Windsor, NS · Canada-Nova Scotia-Windsor
- Full-time
Ability to lead a project within QC, including collaborating with internal and external clients, auditors and presenting data and results clearly and concisely.
Added 1 month ago
TF
Facility Cleaner II - Afternoon Shift
Thermo Fisher Scientific
Mississauga, ON
- Full-time
…members, modelling positive team principles and partnering to meet project and departmental objectives. Carry out all duties within strict compliance to Patheon quality systems Standard…
Added 2 months ago
TF
Automation and Digital Projects Specialist
Thermo Fisher Scientific
Mississauga, ON
- Full-time
Working knowledge of Good Manufacturing Practices (GMP), GAMP 5, 21 CFR Part 11, and computer system validation principles. Understanding of automation concepts, system integrations, APIs,…
Added 2 months ago
TF
Sr EHS Specialist & Industrial Hygienist
Thermo Fisher Scientific
Whitby, ON
- Full-time
…members, modelling positive team principles and partnering to meet project and departmental objectives. Perform all duties within strict compliance to Patheon quality systems Standard…
Added 3 months ago
JP
Chef de service, systèmes qualité / Sr. Manager, Quality Systems and Compliance
Jubilant Pharma Limited
Montreal, Quebec
- Full-time
Added 3 months ago
AG
Director, Quality Assurance
AtomVie Global Radiopharma
Hamilton, ON
- Full-time
AtomVie Global Radiopharma Inc. is a global leading GMP manufacturer and distributer of clinical and commercial radiopharmaceuticals. We work with our partners to transform patients’ lives…
Added 3 months ago
R
Project Engineer/Senior Specialist, Project Engineering
Resilience
Mississauga, Ontario · CAN - ON - Mississauga - Meadowpine Blvd
- Full-time
The Project Engineer/Senior Specialist, Project Engineering leads the execution of complex engineering projects in a GMP biopharmaceutical environment, exercising independent technical…

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CRB

Design Project Manager

Mississauga, ON, Canada

$122,000 to $160,000 CAD / year · Full-time

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Job details

Pay: $122,000 to $160,000 CAD / year
Job type: Full-time
Experience: 5+ years of experience in design project management, preferably in pharmaceutical or biotech facility design.
Posting language: English
Posted: Sep 21, 2026

Original job description

Company Description

At CRB, we design and build some of the most powerful facilities in the world - those that change people's lives. We are the leading provider of sustainable Engineering, Architecture, Construction and Consulting solutions to the global life sciences and food and beverage industries. Our employees provide best-in-class solutions that drive success and positive change for our clients, our people and our communities. CRB is a privately held company with a rich history of serving clients throughout the world, consistently striving for the highest standard of technical knowledge, creativity and execution.

Job Description

The Design Project Manager will lead multidisciplinary design teams in delivering innovative, compliant, and efficient facility solutions for clients in the life sciences, biotechnology, and pharmaceutical sectors. This role is pivotal in ensuring design excellence, client satisfaction, and seamless integration between architecture, engineering, and construction.

Responsibilities

Manage the design phase of complex facility projects from concept through construction documentation, ensuring alignment with client goals, regulatory requirements, and CRB’s quality standards.
Serve as the primary design liaison with clients, facilitating clear communication, managing expectations, and ensuring satisfaction throughout the project lifecycle.
Lead and coordinate internal design teams (architects, engineers, consultants) and external partners to deliver integrated solutions on schedule and within budget.
Define project scope, develop design budgets, and monitor progress to ensure financial and operational targets are met.
Ensure all designs meet applicable codes, standards, and industry regulations, including GMP, FDA, and EU Annex 1 requirements.
Promote the use of cutting-edge technologies and sustainable design practices, including CFD modeling, energy-efficient systems, and modular construction strategies.
Identify design risks early and implement mitigation strategies to avoid delays or cost overruns.

Qualifications

Bachelor’s or Master’s degree in Architecture, Engineering, or related field.
5+ years of experience in design project management, preferably in pharmaceutical or biotech facility design.
Strong understanding of GMP, cleanroom design, and regulatory environments.
Proven ability to lead cross-functional teams and manage multiple projects simultaneously.
Excellent communication, negotiation, and organizational skills.
Proficiency in design software (Bluebeam, Navisworks) and project management platforms.

Additional Qualifications

PMP or similar project management certification.
Familiarity with progressive contracting and integrated project delivery (IPD) models.

Additional Information

We are an equal opportunity employer and value diversity. All employment is decided on the basis of qualifications, merit, and business need.

Your privacy is important to us. All personal information collected will be kept strictly confidential in accordance with applicable Canadian privacy legislation.

CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please, no phone calls or emails.

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Compensation: CAD 122000 - CAD 160000 - yearly

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More about this job

Responsibilities

The Design Project Manager will lead multidisciplinary teams to deliver innovative and compliant facility solutions for life sciences and pharmaceutical clients. This role involves managing project scope, budgets, and schedules while serving as the primary liaison between clients and internal design teams.

Requirements

Candidates must hold a Bachelor’s or Master’s degree in Architecture or Engineering with at least 5 years of experience in design project management. Proficiency in industry-standard design software and a strong understanding of GMP and regulatory environments are required.

Skills

Project Management
Design Management
Life Sciences
Biotechnology
Pharmaceutical
GMP
Cleanroom Design
Regulatory Compliance
Bluebeam
Navisworks
Cross-functional Team Leadership
Budget Management
Construction Documentation
Integrated Project Delivery
Stakeholder Management

Visa sponsorship

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Keywords

Design Project Manager
Engineering
Architecture
Construction
Consulting
Life Sciences
Biotechnology
Pharmaceutical
GMP
FDA
EU Annex 1
CFD Modeling
Modular Construction
Bluebeam
Navisworks
PMP
Integrated Project Delivery
Facility Design
Regulatory Compliance
Budgeting
Risk Mitigation
Sustainable Design

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