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The Valens Company: Quality Assurance Associate – Compliance

The Valens Company

This is a Contract position in Montreal, QC posted February 21, 2021.

Reporting to the Director, Compliance, the Quality Assurance Associate Compliance is responsible for learning, teaching, implementing, and enforcing SOP compliance in all departments, as related to external quality systems.

As the QA Associate Compliance you would be responsible for customer complaints, vendor management, internal and external audits, stability, and risk assessments.Duties:Assists the Director, Compliance in managing the Quality Management System (QMS) as related to external quality systemsWrites, reviews, and updates SOPs and policies to ensure continuous complianceEnsures and monitors adherence to SOPs relating to current GMPs and other applicable regulations; including but not limited to, customer complaints, vendor management, internal and external audits, stability, and risk assessmentsEnsures and enforces Good Documentation Practices on all applicable documents relating to GMPsResponsible for training of employees on applicable SOPs and GMP related topics.Support internal and external audits for Health Canada, GMP and QA, including addressing issues, preparing response reports, and implementing CAPAsManage and assists in the investigations of customer complaints and determine and implement appropriate CAPAsManage the vendor management program, establish scope for vendors and approve or disqualify vendorsAssist in planning, conducting, and reporting of external audits of vendors, partners, and service providersDevelop stability protocols and analyze resultsParticipate in risk assessmentsInitiate, review, and assess Change Controls as part of a cross-functional teamEnsure reporting, registration, filing, and other administrative tasks are completed in a timely fashionComplete all other tasks related to the position, as assigned by Director, Compliance.Qualifications:Bachelor of Science Degree (BSc) in applicable field2-5 years of work experience in a related field requiredKnowledge of GMP, ISO 9001, and Health Canada cannabis regulationsPrevious experience in either the cannabis or pharmaceutical industry an assetKnowledge of GLP principles, ISO 17025, and laboratory experience an assetKnowledge and experience in chemistry, and pharmacology an assetStrong knowledge of MS Word, Excel and OutlookExcellent analytical skills and above average attention to detailExcellent time management and prioritization skillsCapable of multitasking with minimal supervisionExcellent English communication skills, both written and verbalAbility to complete a satisfactory criminal record checkWe offer a welcoming and friendly space for BIPOC & LGBTQ applicants.