Located in Barrie, Ontario, 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, named Start-Up of the Year at the most recent Canadian Cannabis Awards. Our growing team of scientists, technicians, engineers and business professionals delivers quality and innovation through research, discipline, and forward thinking. The Quality Systems Associate will provide quality oversight to the functions within the quality systems for the site. The quality systems that this role will support are product complaints, deviation management, change controls, corrective actions, internal/external audits and supplier qualification. In order to succeed in this role, the associate must have strong investigation and technical writing skills to work in collaboration with production to resolve quality issues.Responsibilities:Conduct product complaint investigations including manufacturing record reviews and sample analysis in conjunction with the Quality Assurance Person Perform qualification activities of new vendors and maintain vendor files Assist with conducting internal and external audits  Manage implementation of corrective/preventative actions (CAPAs) as required and follow up with internal departments to ensure timeliness of implementation Perform data analysis on quality systems to support data trending and management review Author and review quality documents including standard operating procedures, forms, and batch production records Champion the change control system and document management Assist individuals with the electronic quality management system and host training sessions for new users Perform deviation investigations to identify root cause and corrective actions. Follow up with other departments to ensure deviation investigations are completed on time Analyze data to identify trends and report issues to Quality Systems Manager Work as part of the Quality Assurance team promoting a quality culture within the company Skills/ Qualifications:Investigation skills; with an understanding of root cause analysis and ability to lead and support critical investigations Strong technical writing skills Effective communication and teamwork skills Experience in areas of Quality Systems: Change Controls, Deviations, CAPAs, Document Control, Product Complaints Bachelor’s degree or diploma in science related field1 year Quality experience is an asset

Quality Systems Associate

Located in Barrie, Ontario, 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, named Start-Up of the Year at the most recent Canadian Cannabis Awards. Our growing team of scientists, technicians, engineers and business professionals delivers quality and innovation through research, discipline, and forward thinking. 

The Quality Systems Associate will provide quality oversight to the functions within the quality systems for the site. The quality systems that this role will support are product complaints, deviation management, change controls, corrective actions, internal/external audits and supplier qualification. In order to succeed in this role, the associate must have strong investigation and technical writing skills to work in collaboration with production to resolve quality issues.

Responsibilities:

  • Conduct product complaint investigations including manufacturing record reviews and sample analysis in conjunction with the Quality Assurance Person 
  • Perform qualification activities of new vendors and maintain vendor files 
  • Assist with conducting internal and external audits  
  • Manage implementation of corrective/preventative actions (CAPAs) as required and follow up with internal departments to ensure timeliness of implementation 
  • Perform data analysis on quality systems to support data trending and management review 
  • Author and review quality documents including standard operating procedures, forms, and batch production records 
  • Champion the change control system and document management 
  • Assist individuals with the electronic quality management system and host training sessions for new users 
  • Perform deviation investigations to identify root cause and corrective actions. Follow up with other departments to ensure deviation investigations are completed on time 
  • Analyze data to identify trends and report issues to Quality Systems Manager 
  • Work as part of the Quality Assurance team promoting a quality culture within the company 

Skills/ Qualifications:

  • Investigation skills; with an understanding of root cause analysis and ability to lead and support critical investigations 
  • Strong technical writing skills 
  • Effective communication and teamwork skills 
  • Experience in areas of Quality Systems: Change Controls, Deviations, CAPAs, Document Control, Product Complaints 
  • Bachelor’s degree or diploma in science related field
  • 1 year Quality experience is an asset

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