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Quality Assurance and Pharmacovigilance Associate

Bekijk en reageer bij Brunel Engineering (externe link)

Quality Assurance & Pharmacovigilance Associate (12-month contract) hybride in Toronto, ON.

Locatie
Toronto, CA
Werkvorm
hybride
Contractvorm
detachering
Sluitingsdatum
Eerste waarneming
Uitgezet via
Brunel

Eisen

Wensen

Omschrijving

Quality Assurance & Pharmacovigilance Associate (12-month contract) hybride in Toronto, ON. Support pharmacovigilance and quality processes in accordance with company procedures and regulatory requirements. Review, process, and maintain safety and quality-related documentation. Monitor, document, and escalate product complaints, adverse events, deviations. Assist with investigations, root cause analysis, CAPAs. Maintain records in quality and safety management systems. Collaborate with regulatory, medical, quality, and operations teams. Support audits and compliance activities. Requirements: Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Chemistry, or related; 3-5 years experience in pharmacovigilance, quality assurance/control, regulatory affairs; understanding of GxP; experience reviewing regulated documentation; strong communication; proficiency with electronic quality/safety systems is an asset. Experience supporting both quality and pharmacovigilance in small/mid-sized org is an asset. Closing: October 19, 2026.

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