Назад
Company hidden
3 дня назад

QA Reviewer

50 000CAD
Формат работы
onsite
Тип работы
fulltime
Английский
c1
Страна
Canada
Релокация
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
QA Reviewer (GMP/ISO 17025): Ensuring compliance and reviewing quality documentation for biopharma testing services with an accent on GMP, GLP, ISO 17025, audits, and laboratory data accuracy. Focus on conducting deviations, CAPA, out-of-specification, and change control investigations while maintaining quality systems and accreditation.

Location: Toronto, Ontario, Canada; relocation to Mississauga, Ontario, expected in 2026. The role is performed in office and laboratory environments, with occasional evening or weekend work.

Compensation: up to CAD 50,000 yearly.

Company

hirify.global is an international life sciences network providing analytical testing, laboratory, biopharma, pharmaceutical, food, environmental, and other scientific services.

What you will do

  • Review quality documents, laboratory data, validation studies, logbooks, calibration reports, training records, and final reports.
  • Maintain the Quality System by drafting and updating procedures and tracking GMP and ISO 17025 documentation.
  • Support and conduct internal and external audits, including managing the internal auditing program when required.
  • Log and investigate complaints, deviations, out-of-specification results, Corrective Action and Preventative Action (CAPA), and Change Control activities.
  • Evaluate instrumentation data, prepare reports, and communicate deficiencies and improvement areas to department staff.
  • Support staff training, SOP circulation, accreditation maintenance, record keeping, and compliance monitoring.

Requirements

  • Knowledge of ISO 17025 and GMP requirements.
  • Fluent written and spoken English required.
  • Degree or diploma in a science-related discipline.
  • Strong communication, organizational, multitasking, accuracy, and attention-to-detail skills.
  • Ability to work independently in a collaborative department and handle confidential matters professionally.
  • High proficiency in Microsoft Office, especially Excel.

Nice to have

  • Previous GMP experience.
  • Willingness and ability to learn quickly and apply knowledge to different scenarios.

Culture & Benefits

  • Full-time employment with health and dental coverage.
  • Life and disability insurance.
  • RRSP with a 3% company match.
  • Paid holidays and paid time off.
  • Work in office and laboratory environments within a collaborative, quality-focused department.

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