MediPharm Labs offers a professional and collaborative workplace culture in a leading-edge facility built to international pharma standards. Our company is a recognized leader in the Cannabis industry, having won numerous cannabis and entrepreneurial awards. Our growing team of scientists, technicians, engineers, and business professionals delivers quality and innovation through research, discipline, and forward thinking. Qualifications and SkillsAssisting the QA Manager (Quality Assurance Person) in managing the Quality Management System (QMS)• Assisting the QA Manager with overseeing the QA Technicians (Project Team) to ensure responsibilities of the QA Department are maintained• Ensures the day to day QA tasks related to Medical channel fulfilment are carried out• Work with QA Technicians and Manufacturing to ensure PCP documents are completed and maintained for all manufacturing processes• Ensure compliance with the Cannabis Act, Controlled Drugs and Substances Act (CDSA), Narcotics Control Regulations (NCR), Pest Control Products Act (PCPA), Fertilizer Act, 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• 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, edible cannabis, and live cannabis plants• Assist in investigation of quality related issues and the preparation of quality related reports (CAPA, Deviation and Investigation)• Assist with entering information/data into the computer records/ERP• Assist with regulatory audits by attending meetings and providing aid for any follow-up actions, as required• Work with the QAP to ensure GPP requirements are being met for documentation, qualification, and validation• Other duties, as assigned by the QA ManagerAcademic/Educational Requirements• BSc or Diploma or degree in a science related field and/or relevant industry experienceRequired Skills/Experience/Knowledge• 1-3 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• Previous Health Canada Security Clearance and work experience with a Canadian Licensed Producer (LP) is considered as an asset• Capable of multi-tasking 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 multi-task• Excellent attention to detail• Experience with technical report writing and scientific documents an asset• Must possess excellent communication skills for liaising and communicating with internal departments• Excellent critical thinking, problem solving and decision-making skills• Excellent English communication skills (written and verbal)• Team player, works well with others, able to take direction• Motivated to work in a dynamic and fast-paced team environment 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 contact 705-719-7425 ext. 1080

Quality Assurance Associate

MediPharm Labs offers a professional and collaborative workplace culture in a leading-edge facility built to international pharma standards. Our company is a recognized leader in the Cannabis industry, having won numerous cannabis and entrepreneurial awards. Our growing team of scientists, technicians, engineers, and business professionals delivers quality and innovation through research, discipline, and forward thinking. 

Qualifications and Skills

Assisting the QA Manager (Quality Assurance Person) in managing the Quality Management System (QMS)
• Assisting the QA Manager with overseeing the QA Technicians (Project Team) to ensure responsibilities of the QA Department are maintained
• Ensures the day to day QA tasks related to Medical channel fulfilment are carried out
• Work with QA Technicians and Manufacturing to ensure PCP documents are completed and maintained for all manufacturing processes
• Ensure compliance with the Cannabis Act, Controlled Drugs and Substances Act (CDSA), Narcotics Control Regulations (NCR), Pest Control Products Act (PCPA), Fertilizer Act, 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
• 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, edible cannabis, and live cannabis plants
• Assist in investigation of quality related issues and the preparation of quality related reports (CAPA, Deviation and Investigation)
• Assist with entering information/data into the computer records/ERP
• Assist with regulatory audits by attending meetings and providing aid for any follow-up actions, as required
• Work with the QAP to ensure GPP 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
• 1-3 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
• Previous Health Canada Security Clearance and work experience with a Canadian Licensed Producer (LP) is considered as an asset
• Capable of multi-tasking 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 multi-task
• Excellent attention to detail
• Experience with technical report writing and scientific documents an asset
• Must possess excellent communication skills for liaising and communicating with internal departments
• Excellent critical thinking, problem solving and decision-making skills
• Excellent English communication skills (written and verbal)
• Team player, works well with others, able to take direction
• Motivated to work in a dynamic and fast-paced team environment

 

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 contact 705-719-7425 ext. 1080

To apply online, please click on the appropriate link below.