Validation Engineer HVAC & Equipment
- Toronto, ON, Canada
Full-time
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Job details
- Job type
- Full-time
- Apply by
- Experience
- 1–5 years of experience in qualification, validation, commissioning, or engineering projects within the pharmaceutical or other regulated industries.
- Posting language
- English
- Posted
Original job description
We are seeking a Validation Engineer HVAC & Equipment to support HVAC and equipment qualification and validation activities within a pharmaceutical manufacturing environment. In this short-term contract, you will contribute to the preparation, execution, and closure of qualification protocols while ensuring all work meets GMP/cGMP requirements and audit-readiness standards. You will work closely with engineering, quality assurance, facilities, and project teams to deliver validation milestones on schedule.
- Location: Toronto, Ontario
- Support HVAC system qualification and validation activities, including air handling units (AHUs), ductwork, filtration systems, pressure cascades, and environmental monitoring.
- Assist in the preparation, execution, and closure of equipment and HVAC qualification protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
- Prepare and review validation documentation, including qualification protocols, test records, technical reports, and final summary reports, ensuring compliance with GMP/cGMP.
- Review engineering drawings, technical specifications, equipment documentation, and vendor deliverables to verify compliance with project requirements and applicable quality standards.
- Maintain complete, accurate, and traceable qualification and validation records in accordance with Good Documentation Practices (GDP) and audit-readiness requirements.
- Support the development and maintenance of Continuous Validation Plans, ensuring qualification activities and documentation remain current.
- Identify, document, and follow up on deviations, non-conformances, and change controls related to equipment qualification and HVAC systems.
- Collaborate with engineering, quality assurance, facilities, and project teams to support timely completion of qualification and validation deliverables.
- Assist with the review and organisation of HVAC-related software records and supporting documentation, where applicable.
- Ensure assigned activities are completed according to approved procedures, project timelines, and pharmaceutical quality requirements.
- Bachelor's degree or technical diploma in Mechanical Engineering, Chemical Engineering, Industrial Engineering, or a related engineering discipline.
- 1–5 years of experience in qualification, validation, commissioning, or engineering projects within the pharmaceutical or other regulated industries.
- Basic knowledge of HVAC systems, including AHUs, ductwork, filtration systems, pressure cascades, and environmental monitoring.
- Experience supporting equipment qualification activities, including IQ, OQ, and PQ.
- Knowledge of GMP/cGMP and pharmaceutical quality requirements.
- Familiarity with Continuous Validation Plans and the preparation, execution, and maintenance of qualification and validation documentation.
- Ability to review technical drawings, equipment specifications, vendor documentation, and test records.
- Understanding of deviation management, change control processes, and GDP.
- Strong attention to detail and organisational skills, with the ability to maintain accurate, complete, and audit-ready documentation.
- Self-motivated and quick to learn, able to work independently with minimal supervision.
- Fluent in English, with strong written and verbal communication skills.
- Familiarity with HVAC-related software or tools used in engineering, qualification, or validation activities.
65-90K The final compensation offered will be determined based on the candidate’s level of experience, skills, and qualifications, in compliance with applicable pay transparency requirements.
Canadian Experience Requirement:
No Canadian work experience is required for this position. Candidates are encouraged to apply regardless of previous Canadian experience.
Artificial Intelligence (AI) Disclosure:
No Artificial Intelligence (AI) tools are used in the screening, assessment, or selection of candidates for this position. All stages of the recruitment process are conducted by human recruiters and hiring managers.
Statement Regarding Job Vacancy:
This position is a Job creation, created to support ongoing project needs.
Recruitment Process & Feedback Timeline:
Candidates will receive feedback on their application within a maximum of 45 days from the date of application or from their most recent interview stage.
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.)
Who are we?
Amaris Consulting, part of Mantu 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.
At Amaris, we strive to provide our candidates with the best possible recruitment experience. We like to get to know our candidates, challenge them, and be able to give them proper feedback as quickly as possible. Here's what our recruitment process looks like:
Brief Call: Our process typically begins with a brief virtual/phone conversation to get to know you! The objective? Learn about you, understand your motivations, and make sure we have the right job for you!
Interviews (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). During the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. Of course, you will also get to know Amaris: our culture, our roots, our teams, and your career opportunities!
Case study: Depending on the position, we may ask you to take a test. This could be a role play, a technical assessment, a problem-solving scenario, etc.
As you know, every person is different and so is every role in a company. That is why we have to adapt accordingly, and the process may differ slightly at times. However, please know that we always put ourselves in the candidate's shoes to ensure they have the best possible experience.
We look forward to meeting you!
More about this job
Responsibilities
Support HVAC and equipment qualification activities, including preparing, executing, and closing IQ, OQ, and PQ protocols, and reviewing technical and vendor documentation. Maintain accurate, audit-ready validation records and support continuous validation plans, deviation follow-up, change controls, and coordination with engineering, quality, facilities, and project teams.
Requirements
Requires a bachelor's degree or technical diploma in an engineering discipline and 1–5 years of qualification, validation, commissioning, or engineering project experience in a pharmaceutical or other regulated industry. Candidates should have basic HVAC knowledge, experience supporting IQ/OQ/PQ, familiarity with GMP/cGMP, validation documentation, GDP, deviations and change controls, and strong English communication and organizational skills.
Skills
- HVAC Qualification And Validation
- Equipment Qualification
- Installation Qualification (IQ)
- Operational Qualification (OQ)
- Performance Qualification (PQ)
- GMP/cGMP Compliance
- Continuous Validation Plans
- Validation Documentation
- Air Handling Units (AHUs)
- Environmental Monitoring
- Technical Drawing Review
- Deviation Management
- Change Control
- Audit-Ready Recordkeeping
- Vendor Documentation Review
Benefits
- Training And Development
- Internal Academy
- Inclusive Work Environment
Visa sponsorship
Not detected in the job text
Categories
- Engineering
- Manufacturing
- Consulting
Keywords
- HVAC
- Air Handling Units (AHUs)
- Ductwork
- Filtration Systems
- Pressure Cascades
- Environmental Monitoring
- Equipment Qualification
- Installation Qualification (IQ)
- Operational Qualification (OQ)
- Performance Qualification (PQ)
- GMP
- cGMP
- Continuous Validation Plans
- Validation Protocols
- Qualification Documentation
- Deviation Management
- Non-Conformance Management
- Change Control
- Audit Readiness
- Technical Drawings
- Equipment Specifications
- Vendor Documentation
- Pharmaceutical Manufacturing
- Regulated Industries
- HVAC Software