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COMPANY BACKGROUND:
Located in Barrie Ontario MediPharm Labs (TSX: LABS) offers a professional and collaborative workplace culture in a leadingedge facility built to international pharma standards. Our company is a recognized leader in the Cannabis industry having received numerous entrepreneurship and cannabis awards. Our growing team of scientists technicians engineers and business professionals delivers quality and innovation through research discipline and forward thinking.
Position Overview:
The Quality Assurance (QA) Specialist (QMS) will support all aspects of Quality Management System at the site level as directed by the Quality Assurance Manager
Assisting the QA Manager (Quality Assurance Person) in managing the Quality Management System (QMS)
Ensures the daytoday QA tasks related to Veeva eQMS are carried out
Work with MPL staff to ensure Deviations CAPAs and Change Controls are completed within the required timelines including leading biweekly meetings with relevant departments to ensure timely completion of tasks
Ensure compliance with the Cannabis Act Controlled 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 & safety protocols and workplace policies to ensure consistent quality of all cannabis products including but not limited to dried cannabis cannabis extracts and edible cannabis
Assist in investigation of quality related issues and the preparation of quality related reports (CAPA Deviation Change Control and Investigation)
Perform risk assessments and assist in the preparation of annual product quality reviews (APQRs)
Assist with regulatory audits by providing aid for any documentation or followup actions as required
Assist wit Product Complaints log and investigations.
Work with the QAP to ensure GPP/GMP requirements are being met for documentation qualification and validation
Other duties as assigned by the QA Manager
Academic/ Educational Requirements
BSc or Diploma or degree in a science related field and/or relevant industry experience
Required Skills/Experience/Knowledge
Minimum 3 years Quality Assurance experience in GPP/GMP manufacturing fields preferably within Pharmaceutical Legal Cannabis Food Industry or any other relevant industry is considered an asset
Capable of multitasking with minimal supervision
Strong computer skills; Proficiency with MS Office Suite especially Excel
Knowledge of quality assurance terminology methods and tools
Strong organizational skills including the ability to manage time set priorities and multitask
Experience with technical report writing and scientific documents is considered an asset
Must possess excellent communication skills for liaising and communicating with internal departments
Excellent critical thinking problem solving and decisionmaking skills
Team player works well with others able to take direction
Prior experience with Veeva or other eQMS is considered an asset
About MediPharmLabs
Founded in 2015 MediPharm Labs specializes in the development and manufacture of purified pharmaceuticalquality cannabis concentrates active pharmaceutical ingredients (API) and advanced derivative products utilizing a Good Manufacturing Practices certified facility with ISO standardbuilt clean rooms. Through its wholesale and white label platforms MediPharm Labs formulates develops processes packages and distributes cannabis extracts and advanced cannabinoidbased products to domestic and international markets.
In 2023 MediPharm acquired VIVO Cannabis Inc. which expanded MediPharms reach to medical patients in Canada via the Canna Farms medical ecommerce platform in Australia and Germany through Beacon Medical PTY and Beacon Medical GMBH. This acquisition also included Harvest Medical Clinics in Canada which provides medical cannabis patients.
MediPharm Labs is committed to providing accommodation for applicants with disabilities in its recruitment processes. If you require accommodation at any time during the recruitment process please contactext. 1080
Required Experience:
Unclear Seniority
Full-Time