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3 дня назад

Validation Engineer HVAC & Equipment

65 000 - 90 000CAD
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
c1
Страна
Canada
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Validation Engineer HVAC & Equipment (HVAC/Pharmaceutical Manufacturing): Supporting HVAC and equipment qualification and validation activities in a pharmaceutical manufacturing environment with an accent on GMP/cGMP compliance, IQ/OQ/PQ protocols, and audit-ready documentation. Focus on reviewing technical drawings and vendor deliverables, managing deviations and change controls, and maintaining Continuous Validation Plans.

Location: Toronto, Ontario, Canada

Expected compensation: CAD 65,000–90,000 per year

Company

hirify.global is an independent technology consulting firm providing guidance and solutions across engineering, life sciences, information systems, and telecommunications.

What you will do

  • Support qualification and validation of HVAC systems, including AHUs, ductwork, filtration systems, pressure cascades, and environmental monitoring.
  • Prepare, execute, and close equipment and HVAC qualification protocols, including IQ, OQ, and PQ.
  • Prepare and review qualification protocols, test records, technical reports, and final summary reports in compliance with GMP/cGMP.
  • Review engineering drawings, technical specifications, equipment documentation, and vendor deliverables against project and quality requirements.
  • Maintain complete, accurate, traceable, and audit-ready records in accordance with Good Documentation Practices.
  • Support Continuous Validation Plans, deviation and non-conformance follow-up, change controls, HVAC software records, and cross-functional delivery with engineering, quality assurance, facilities, and project teams.

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 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 qualification and validation documentation.
  • Ability to review technical drawings, equipment specifications, vendor documentation, and test records.
  • Understanding of deviation management, change control processes, and Good Documentation Practices.
  • Strong attention to detail and organisational skills, with the ability to maintain accurate, complete, and audit-ready documentation.
  • Self-motivated, quick to learn, and able to work independently with minimal supervision.
  • Fluent English with strong written and verbal communication skills.
  • Familiarity with HVAC-related software or tools used in engineering, qualification, or validation activities.
  • No Canadian work experience is required.

Culture & Benefits

  • International community representing more than 110 nationalities, with teams across more than 60 countries.
  • Trust-focused environment with 70% of leaders having started at entry level.
  • Internal Academy with more than 250 training modules.
  • Dynamic environment with internal events such as afterworks and team buildings.
  • Equal-opportunity and inclusive workplace.

Hiring process

  • Brief virtual or phone call.
  • Approximately three interviews, varying by seniority.
  • Potential case study, technical assessment, role play, or problem-solving exercise.
  • Application feedback provided within a maximum of 45 days from application or the latest interview stage.

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