3 дня назад
QA Reviewer
50 000CAD
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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