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Bilingual - Quality Assurance Associate
Visualizza: 192
Giorno di aggiornamento: 12-06-2024
Località: Quebec City Québec
Categoria: Garanzia di qualità / Controllo di qualità
Industria: Construction Management Consulting Pharmaceuticals
Posizione: Entry level
Tipo di lavoro: Full-time
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Contenuto del lavoro
Quality Assurance AssociateZany Consulting Group
Build a better career with Zany Consulting Group
Serving customers and community starts with the most talented people doing their very best work. That is precisely what we have at Zany Consulting Group, a leading Professional Services Consulting firm. Zany Consulting Group is seeking exceptionally driven, experienced Quality Assurance Associateto undertake projects for one of our clients in Toronto, Ontario.
In This Role
Contribute to establishing and maintaining high quality and compliance status of all products handled by Sanofi Canada to meet all Canadian cGMP regulations as well as Corporate requirements.
Responsibilities
- Serve in a backup capacity to QA Manager and other QA Specialists for their respective responsibilities.
- Plan and coordinate daily, weekly and monthly release activities.
- Coordinate the Change Control Program of manufacturing sites
- Evaluate and approve investigations
- Provide QA expertise to internal and external partners
- Collect, review and approve all required documentation necessary for product release, including batch documentation review
- Inspect and release products and APIs on the Canadian market
- Inspect products, review documentation and release Clinical Supply Materials, products under the programs Special Access to Drugs and Health Products and Access to Drugs in Exceptional Circumstances
- Coordinate and maintain specifications and methods
- Send products for testing, approve results and support laboratories, if required
- Issue Change Requests, Deviations, Investigations and CAPAs
- Act as QPIC backup and perform all related activities
- Support MedInfo requests
- Other QA duties, as assigned
Skills and Qualifications:
- B.Sc. in Chemistry, Biology or related sciences
- 3 years of relevant experience in the pharmaceutical industry (QA, QC, Production or equivalent)
- Extensive knowledge of Canadian GMPs
- Excellent analytical and problem-solving abilities
- Team player
- Ability to maintain good interpersonal relationships
- Ability to set priorities
- Good communication skills (verbal and written)
- French and English written and spoken
Equal Opportunity Statement:All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation or gender identity.
Job Type: Contract
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Scadenza: 27-07-2024
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