Specialist Quality Systems (QS) - Stability
On-site · Knowlton, Québec, Canada
Job Summary
Specialist Quality Systems (QS) – Stability leads the marketed stability program for OTC, natural health, and cosmetic products, initiating/preparing stability protocols, interim/final stability reports, OOS investigations, and stability specifications in LIMS. You will manage stability studies, coordinate equipment/resources, and ensure data quality and documentation for internal and external stakeholders, while contributing to continuous improvement of laboratory processes in a regulated GMP environment. Ideal candidates hold a DEC in Science (associates level) with 2+ years of GMP laboratory experience, strong Excel/Outlook/Word skills, LIMS familiarity, and bilingual French/English communication.
Required Qualifications
- A Diploma of Collegial Studies (DEC) in Science
- Bachelor of Science (B.Sc.) is an asset
- Minimum of two (2) years of laboratory experience in a regulated environment (GMP)
- Experience with a LIMS system is an asset
- Bilingualism in French and English (oral and written) is required to communicate with team members and clients' technical documentation
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