Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
Очень мало
65к-90к CAD/год
110к CAD120к CADмедиана150к CAD
По похожим ролям (50) ~ 120к CAD/год
43
Не очень вакансия
развернуть
Обязанности понятны и дают полезный опыт в фармацевтической валидации, но зарплата заметно ниже рыночного ориентира, а указание на краткосрочный контракт противоречит отметке о постоянной работе.
Кликните для подробной информации
Ниже рынкаНеясный форматПроектная работаПонятные задачиОбучение внутри
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
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.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →