Назад
Company hidden
6 дней назад

Quality Assurance Specialist Days (Biopharma)

76 200 - 110 100CAD
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
Canada
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Quality Assurance Specialist Days (Biopharma): Ensuring GMP compliance, reviewing quality documentation, and supporting batch and product quality operations in a pharmaceutical manufacturing environment with an accent on audits, regulatory readiness, and shopfloor quality oversight. Focus on leading root cause investigations, implementing corrective and preventive actions, and managing quality risks across production processes.

Location: Toronto, ON, Canada; onsite day shift from 8 AM to 4 PM, Friday to Tuesday

Salary: CAD 76,200–110,100 per year

Company

hirify.global is an R&D-driven biopharmaceutical company developing medicines and vaccines, with a focus on immune-system science and AI-enabled innovation.

What you will do

  • Ensure production and quality activities comply with GMP, GxP, and applicable regulatory requirements.
  • Conduct audits, shopfloor quality oversight, and documentation reviews across manufacturing operations.
  • Investigate quality incidents, lead root cause analysis, and implement corrective and preventive actions.
  • Monitor quality metrics, manage quality risks, and support continuous improvement initiatives.
  • Support internal and external audits, regulatory inspections, and designated APU or PCU units.
  • Collaborate with production and cross-functional stakeholders to maintain product quality throughout the lifecycle.

Requirements

  • Bachelor’s degree or higher in pharmacy, chemistry, biochemistry, life sciences, chemical engineering, engineering, or a related scientific field.
  • 2–5+ years of experience in pharmaceutical quality assurance or operations.
  • Experience with drug substance or drug product quality operations in a regulated pharmaceutical environment.
  • Working knowledge of cGMP, GxP, quality systems, change control, and regulatory requirements.
  • Experience with quality documentation, process improvement, quality investigations, inspection readiness, and risk management.

Culture & Benefits

  • Supportive, future-focused environment centered on scientific progress and continuous improvement.
  • Career development opportunities through promotion or lateral international moves.
  • Rewards package recognizing employee contributions.
  • Healthcare, prevention, wellness, and family-support benefits.
  • Equal opportunity workplace with accommodations available during recruitment.

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 →