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Aurora Cannabis Inc. is a world-renowned integrated cannabis company with an industry-leading reputation for continuously elevating and setting the global cannabis industry standard.

Through our wholly owned subsidiaries, strategic investments, and global partnerships, Aurora provides a wide range of premium quality cannabis and hemp products and services, develops innovative technologies, promotes cannabis consumer health and wellness, and delivers an exceptional customer experience across all its brands.

Aurora’s operations span multiple continents and focuses on both the medical and recreational cannabis production and sales, patient education and clinic counselling services, home hydroponic cultivation, extraction technologies and delivery systems, and hemp-based food health products.

We operate around the globe pursuing new and emerging cannabis markets where possible through our owned network of import, export and wholesale distributors, our e-commerce and mobile applications, brick and mortar retail stores, as well as grocery store retailers, and pharmacies.    

 

Quality Technical Writer

 

Location: Bradford, ON

 

Aurora Cannabis Inc. is currently looking for a Technical Writer to join our team. The successful candidate will be required to have some flexibility in their schedule to meet the needs of the facility. The incumbent will report directly to the Quality Assurance Manager at River (Bradford, ON) and will be responsible for the following:

 

RESPONSIBILITIES:

  • Promote positive safety culture through participation, and adherence to, HSE programs
  • Promote positive working relationships with all departments
  • Develop and/or maintain data-driven logs to support ongoing tracking of metrics
  • Initiate consolidation, or standardization, continuous improvements in the department
  • Interpret highly technical information and tailor to end user as needed
  • Interact with site eQMS to plan, develop, write, and edit procedures and protocols
  • Maintain knowledge of applicable regulations, or other requirements, at site
  • Maintain site core Quality documents or policies, as applicable:
    • Quality Manual
    • Site Master File
    • Quality Management System
  • Interact with SMEs as required, to assure document content accuracy
  • Participate in Preventive Control Plan development and maintenance, as assigned
  • Ensure the timely completion of corrective and preventive actions, as assigned
  • Maintain security and confidentiality of all aspects of the business
  • All other duties as assigned by Manager

 

REQUIREMENTS:

 

  • A least 3 years’ experience working in similar role
  • Excellent written and verbal communication
  • Able to read, interpret and apply regulatory, or other governing, information
  • Able to write in explanatory and procedural styles for multiple audiences
  • Strong soft skills; time management, problem solving, teamwork, communication etc.
  • Proficiency in MS Office programs
  • Ability to work independently, with a strong attention to detail
  • Ability to multitask and adapt to an evolving environment
  • Experience working in a regulated environment, pharmaceuticals, or natural health product manufacturing environment is preferred
  • Experience developing data sets an asset
     

We would like to thank all applications for their interest but only those selected for an interview will be contacted.

 

Aurora is an equal opportunity employer. At Aurora, we are committed to do business inclusively and accommodate applicants with disabilities. If you require accommodation (including, but not limited to, an accessible interview site, alternate format of job posting) during the recruitment and selection process, please let our Recruitment team know.

 


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