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Added 13 mins ago
B
Building Science Engineer
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- Full-time
…specialists to deliver sustainable, practical, and high-performance solutions tailored to the needs of our institutional and commercial…
Added 29 mins ago
T&
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Added 5 hours ago
RW
Junior Consultant
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ON · Richmond Hill Southeast, Ontario
- Full-time
Resolute, the recruitment division of Brevitas, is hiring a Junior Consultant on behalf of Brevitas. Brevitas is dedicated to helping organizations achieve tangible results and lasting…
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Added 9 hours ago
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Added 12 hours ago
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Interior Designer
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Added 22 hours ago
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Added 23 hours ago
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Added 1 day ago
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Added 1 day ago
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Added 1 day ago
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Senior Management Consultant
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Burlington, ON · Kingston, ON · Ottawa, ON · Richmond Hill, ON · Toronto, ON
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Added 1 day ago
FB
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Added 1 day ago
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Added 1 day ago
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Resolute Workforce Solutions

Junior Consultant

ON, Canada
Richmond Hill Southeast, ON, Canada

Annual salary for this role ranges from $50,000 to $60,000, based on experience. · Full-time

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Job details

Pay: Annual salary for this role ranges from $50,000 to $60,000, based on experience.
Job type: Full-time
Experience: 1 to 3 years of relevant experience in engineering, commissioning, qualification, validation, or project coordination.
Posting language: English
Posted: Nov 1, 2026

Original job description

About Brevitas

Resolute, the recruitment division of Brevitas, is hiring a Junior Consultant on behalf of Brevitas. Brevitas is dedicated to helping organizations achieve tangible results and lasting improvements through successful project delivery, continuous process improvement, and effective change management. Our expertise is in Project Management, Engineering, Commissioning & Qualification, Validation, Quality Systems, and Regulatory Affairs.

Role Overview

We are looking for a motivated and energetic Junior Consultant to join our team. You will support project execution and provide engineering and Commissioning, Qualification, and Validation (CQV) support for pharmaceutical facilities, equipment, and systems. You will work alongside experienced consultants to develop your technical skills and contribute to project delivery within regulated life sciences environments.

You will build a well-rounded skill set across several disciplines and be deployed on new client opportunities as they come up. Over time you will work across:

Commissioning, Qualification and Validation (CQV), Computer System Validation (CSV) for pharmaceutical facilities, equipment and systems.
Project management and coordination (PM / PC).
Technical writing, including protocols, reports and procedures.

You will rotate across projects to build these skills. Around year 3, you will shape your path toward the areas you are strongest in and enjoy most.

Responsibilities

Support project planning, coordination and execution across the project lifecycle.
Execute CQV protocols, document and follow up on deviations, and prepare summary reports.
Prepare, review and maintain technical documents, procedures, reports and project deliverables.
Apply engineering principles, established procedures, industry standards and Good Manufacturing Practices (GMP).
Maintain project schedules, task lists, progress reports and project documentation.
Take ownership of assigned deliverables, delivering them on time and seeking guidance from senior team members early on unfamiliar technical challenges.
Participate in project meetings, technical discussions and knowledge-sharing activities

Requirements

Qualifications

Bachelor's degree in engineering, preferably Chemical, Mechanical, Biotechnology, or a related discipline (or equivalent).
1 to 3 years of relevant experience in engineering, commissioning, qualification, validation, or project coordination.
Experience in pharmaceutical, biotechnology, life sciences, or regulated manufacturing environments is an asset.
Legally entitled to work in Canada.

Skills

Understanding of engineering principles.
Familiarity with Microsoft Excel, Word, PowerPoint, and project management tools.
Strong organizational skills, attention to detail, and the ability to manage multiple assigned tasks.
Good written and verbal communication skills, with the ability to collaborate with team members and stakeholders.
Willingness to learn, take initiative, accept feedback, and develop technical capabilities.
Ability to work collaboratively, follow established procedures, and meet project deadlines.

Work Environment

Work is delivered at client sites, hybrid, or from our Richmond Hill, ON office, depending on the project and client.
Client sites are within the GTA. some travel to client facilities may be required.
Some client sites require clean room access and gowning.
Assignments depend on our project pipeline. Expect variety, and some changes in setting and scope between projects.
You will work alongside experienced consultants and receive guidance on unfamiliar challenges.

Benefits

Annual salary for this role ranges from $50,000 to $60,000, based on experience.

Upon successful completion of probation, you will also be enrolled in our benefit programs:

Life Insurance
Accidental Death
Long Term Disability
Dental and Healthcare

About Brevitas

Role Overview

You will build a well-rounded skill set across several disciplines and be deployed on new client opportunities as they come up. Over time you will work across:

Commissioning, Qualification and Validation (CQV), Computer System Validation (CSV) for pharmaceutical facilities, equipment and systems.
Project management and coordination (PM / PC).
Technical writing, including protocols, reports and procedures.

You will rotate across projects to build these skills. Around year 3, you will shape your path toward the areas you are strongest in and enjoy most.

Responsibilities

Support project planning, coordination and execution across the project lifecycle.
Execute CQV protocols, document and follow up on deviations, and prepare summary reports.
Prepare, review and maintain technical documents, procedures, reports and project deliverables.
Apply engineering principles, established procedures, industry standards and Good Manufacturing Practices (GMP).
Maintain project schedules, task lists, progress reports and project documentation.
Take ownership of assigned deliverables, delivering them on time and seeking guidance from senior team members early on unfamiliar technical challenges.
Participate in project meetings, technical discussions and knowledge-sharing activities

Apply About employer

More about this job

Responsibilities

Support project planning, coordination, and execution across the project lifecycle while applying engineering principles and industry standards. Execute CQV protocols, maintain technical documentation, and ensure project deliverables are completed on time.

Requirements

Requires a bachelor's degree in engineering or a related discipline and 1 to 3 years of relevant experience. Candidates must be legally entitled to work in Canada and possess strong organizational and communication skills.

Skills

Project Management
Engineering
Commissioning
Qualification
Validation
Technical Writing
Good Manufacturing Practices
GMP
Computer System Validation
CSV
Project Coordination
Regulatory Affairs
Quality Systems
Microsoft Excel
Microsoft Word
Microsoft PowerPoint

Benefits

Life Insurance
Accidental Death
Long Term Disability
Dental
Healthcare

Visa sponsorship

Not detected in the job text

Keywords

Consulting
Pharmaceutical
Biotechnology
Life Sciences
CQV
CSV
Project Lifecycle
Technical Documentation
GMP
Engineering Principles
Regulatory Affairs
Quality Systems
Commissioning
Qualification
Validation
Project Coordination
Chemical Engineering
Mechanical Engineering
Biotechnology Engineering
Regulated Manufacturing

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