Назад
Company hidden
5 дней назад

Quality Associate-II, QA Assurance (Monday to Friday 10:00h-18:30h)

86 400 - 129 600CAD
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 Associate-II, QA Assurance (GMP/manufacturing): Supporting product quality operations at a healthcare manufacturing plant with an accent on GMP compliance, quality investigations, and change control. Focus on managing non-conformances, approving corrective and preventive actions, controlling defective materials, and serving as an SME for electronic batch records and SPC.

Location: Onsite in Alliston, Ontario, Canada; Monday to Friday, 10:00–18:30 EST. Plant overtime and planned shutdown support may be required.

Salary: CAD 86,400–129,600 annually, including base salary and estimated target incentive payout.

Company

hirify.global develops and manufactures healthcare products focused on saving and sustaining lives.

What you will do

  • Provide frontline support on product quality issues and maintain GMP, regulatory, and procedural compliance.
  • Review and approve procedural changes, product quality concerns, reinspections, new product introductions, and protocols.
  • Initiate, investigate, and approve non-conformance events in the TrackWise system.
  • Follow up on quality exceptions and preventive and corrective actions.
  • Perform change control assessments, executions, and approvals.
  • Control defective work-in-process materials, including quarantine, retention, disposal, segregation, movement, and documentation.

Requirements

  • Bachelor of Science degree or equivalent experience.
  • 3–5 years of experience in manufacturing and quality roles.
  • Prior experience in a GMP setting and knowledge of cGMP, ISO, and regulatory standards.
  • Technical experience with electronic batch records and SPC, or equivalent systems.
  • Strong written and verbal communication, negotiation, collaboration, analytical, and problem-solving skills.
  • Intermediate to advanced proficiency in Microsoft Office Suite and the ability to balance multiple priorities.

Nice to have

  • 5+ years of experience across multiple manufacturing areas.
  • Experience in pharmaceutical, healthcare, or food manufacturing.
  • Experience with continuous improvement methods, Lean 6S, Kaizen, TPM, or DMAIC.

Culture & Benefits

  • Work in a quality-focused healthcare manufacturing environment.
  • Collaborate with internal and external partners across organizational levels.
  • Take ownership of quality outcomes within a global operation.
  • Participate in a workplace built around reliability, ethics, accountability, and continuous improvement.
  • Compensation includes base salary and an estimated target payout under the Management Incentive Compensation Plan.

Hiring process

  • Qualified candidates may be interviewed as part of the recruitment process.
  • Interview outcomes will be communicated within 45 days of the interview.

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 →