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Company Description

nFounded in2015, MediPharm Labs specializes in the development and manufacture of purified, pharmaceutical-quality cannabis concentrates, active pharmaceutical ingredients (API) and advanced derivative products utilizing a Positive Manufacturing Practices certified facility with ISO standard-built clean rooms. MediPharm Labs has invested in an expert, research driven team, state-of-the-art technology, downstream purification methodologies and purpose-built facilities for delivery of pure, trusted and precision-dosed cannabis products for its customers. MediPharm Labs develops, formulates, processes, packages and distributes cannabis and advanced cannabinoid-based products to domestic and international medical markets.n

In 2021,MediPharm Labs received a Pharmaceutical Drug Establishment License from Health Canada, becoming the only company in North America to hold a commercial-scale domestic Good Manufacturing Practices License for the extraction of multiple natural cannabinoids. This GMP license was the first step in the Company's current foreign drug manufacturing site registration with the US FDA. In 2023,MediPharm acquired VIVO Cannabis Inc. which expanded MediPharm's reach to medical patients in Canada via Canna Farms medical ecommerce platform, and in Australia and Germany through Beacon Medical PTY and Beacon Medical GMBH.

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This acquisition also included Harvest Medical Clinics in Canada which provides medical cannabis patients with Physician consultations for medical cannabis education and prescriptions. The Company carries out its operations in compliance with all applicable laws in the countries in which it operates.

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Website

nwww.medipharmlabs.comn

Role Description

nThis is a full-time,



on-site role located in Greater Napanee, ON.n

The Quality

nSupervisor will oversee quality control processes, ensure adherence to quality assurance standards, and manage product quality throughout the production process. The role involves maintaining compliance with regulatory requirements, conducting analytical reviews, troubleshooting quality issues, and driving improvements to meet the company's quality management goals. Collaboration with internal teams to achieve operational excellence is a key aspect of this role.n

Key Responsibilities

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- Report to the Director, Quality and work with the broader Quality and Regulatory teams across all locations
- Manage the Quality Management System (QMS) and provide regular reports to the Director of Quality regarding the status of the quality system.
- Promote a quality environment in a manufacturing industry while ensuring compliance with applicable GPP and GMP regulations.
- Ensures the day-to-day quality tasks related to Veeva eQMS are carried out.
- Provide Support to manufacturing team on day-to-day tasks and act as a leader for the quality and regulatory department
- Provide regulatory support in regard to applicable GPP and GMP regulations as such as Cannabis Act, Cannabis Regulations, Good Manufacturing Practices (GMP), European Good Manufacturing Practices (EU GMP),



Good Agricultural and Collection Practices (GACP).
- Ensure quality reports as Annual Product Quality Review (APQR), Preventive Control Plan (PCP), Pest Control, Environmental Monitoring are performed as per required schedule.
- Support, review and approved Process and Equipment validation and qualification program, ensuring compliance with international validation requirements of GMP.
- Support quality stability program and trending report generation.
- Lead internal and external GPP and GMP site inspections.
- Review of manufacturing records, quality records and incident reports in order to release finished and bulk products for sale.
- Create and verify product quality release documentation such as Certificate of Analysis (CoA), Certificate of Conformance (CoC) and Certificate of Manufacturing (CoM)
- Review product documentation to ensure proper GDP, GPP and GMP procedures were complying during product manufacturing
- Communicate with clients, suppliers and stakeholders in order to coordinate quality documentation and ensure GMP and GPP compliance is followed.
- Work with staff to ensure Deviations, CAPAs and Change Controls are completed within the required timelines including leading meetings with relevant departments to ensure timely completion of tasks
- Ensure compliance with the Cannabis Act, Controlled Drugs and Substances Act (CDSA), Narcotics Control Regulations (NCR), GPP/GMP, and HACCP, and other relevant legislation and standards
- Writing, reviewing, and updating Standard Operating Procedures (SOPs) and quality policies/procedures to ensure continuous compliance with the Cannabis Act and GPP/GMP regulations.
- Enforcing established SOPs and all health

Apply on Kit Job: kitjob.ca/job/2en6kv

📌 Quality Supervisor (Greater Napanee)
🏢 MediPharm Labs
📍 Greater Napanee