Quality Assurance and Regulatory Affairs Associate

PBG BioPharma Inc. is trying to rent a Quality Assurance and Regulatory Associate for our Leduc Alberta location. The place experiences to the Vice President of Product Development and is accountable for the next.

Job Responsibilities:

  • Assists with creating and sustaining extremely organized high quality techniques for manufacturing, packaging, labelling, testing, and launch of pure well being and hashish/hemp merchandise.
  • Prepares, finalizes, and updates insurance policies, procedures, and file kinds associated to those high quality techniques.
  • Assists with getting ready and sustaining Preventative Control Plans (PCPs) for hashish/hemp product manufacturing.
  • Coordinates the event of coaching recordsdata for all workers, ensures required coaching is full and all coaching information are regularly up to date and maintained.
  • Supports workers coaching as wanted.
  • Helps put together certification functions required for Natural Health and Cannabis product manufacturing and distribution in Canada in addition to different international locations as wanted.
  • Supports the reporting of incidents or hostile occasions to regulatory our bodies and upkeep of the corporate’s pharmacovigilance system.
  • Ensures correct file protecting and submitting as per organizational procedures.
  • Assists with monitoring metrics associated to compliance and effectivity of the standard techniques and supplies suggestions for enchancment.

Education and Experience:

  • BSc/MSc in Chemistry/Biochemistry/Biology/Food Science or comparable self-discipline.
  • 2-Three years expertise in a QA/Regulatory manufacturing setting.
  • Experience Quality Management Systems and Preventative Control Plans, and Regulatory Submissions.
  • An understanding of Health Canada/FDA rules and GMP/GPP necessities for any of the next: pharmaceutical, pure well being or hashish merchandise.


  • Strong written and verbal (public talking) communication abilities.
  • High consideration to element and processes.
  • Able to work individually or as a part of a crew.
  • Able to multi-task effectively.
  • Creative thinker.
  • Excellent organizational abilities.
  • Able to speak nicely throughout disciplines.
  • Works nicely in a fast-paced setting with altering a number of priorities and frequent interruptions.
  • Able to comply with course.
  • Efficient with computer systems and laptop applications.

Job Type: Full-time



  • QA/Regulatory manufacturing setting: 2 years (Required)


Work remotely:

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