Quality Assurance Documentation Specialist

GFR Pharma is a manufacturer of natural health supplements and sport nutrition products.  As a proudly Canadian company, we are committed to manufacturing high-quality supplements for our customers. With the continued growth of our business, we are seeking to hire a “Quality Assurance Documentation Specialist”

Main Responsibilities (but not limited to):

  • Obtain and maintain documents required to ensure continuity of Supplier Certification and Raw Material Risk Assessment project.
  • Review and ensure that raw material documents are complete and up-to-date.
  • Prepare raw material and finished product allergen forms as required.
  • Maintain the Supplier and Raw Material Database.
  • Maintain QC-Sales files to ensure Quality-controlled documentation required by Sales is available and up-to-date.
  • Assist in providing documents necessary for submission and maintenance of product and facility certifications.
  • Assist with obtaining and compiling documents for regulatory requirements.
  • Assist with provision of files maintained for the Supplier Certification Program to departments requiring this information, as needed.

Required Qualifications:

  • Diploma or Post-secondary courses in the Sciences.
  • Preference will be given to those with a minimum of two (2) years’ experience in Production or Quality Assurance/Control in a natural health and/or food manufacturing environment.
  • Excellent communication skills, with the ability to establish and maintain relationships.
  • Strong attention to detail and organizational skills.
  • Ability to complete tasks with accuracy, while working within deadlines.
  • Strong analytical, mathematical, and computer skills (MS Excel, Word and Outlook).
  • Team player with the ability to follow-up and maintain a positive attitude.
  • Ability to work with minimal supervision.
  • Knowledge in MS Access would be an asset.

We value our employees and provide a respectful, safe and supportive work environment!  Along with competitive wages, we offer a fully paid comprehensive benefit package upon completion of a 3 month probation period.

If you are interested in joining our team, we look forward to receiving your resume to jobs@gfrpharma.com.  Only individuals selected to be interviewed will be contacted.

Thank you for your interest in GFR Pharma Ltd!


Testimonials

Great first experience manufacturing my product with GFR. I am definitely going to be utilizing your services in the future for more of our products and look forward to our next project with you. Thanks again!
I always prefer to make our products at GFR if possible, because I am confident with your product quality and service for us.

We are growing well steadily in the Korean market and so orders are continuous and items keep increasing.

I really hope to work closely with GFR with most of our products.
James T.President
We cannot wait any longer to express our appreciation for your help during our production process.

We thank you for your professional suggestions and the quick responses to every question we have had; you have been so patient in helping us with every one of our inquiries.

Your guidance throughout the entire product development and production is a tremendous support to us.
Please forward my sincere gratitude to the GFR team. You guys are seriously, seriously on-it!
Chris GFounder
In all my years, I can honestly say, no other company I have ever worked with has provided me with such an unparalleled level of care and service. Literally, GFR Pharma has provided my company with the best level of service I have ever experienced. You are that good, that efficient, that professional.

If there was a problem, it was fixed. If there was a challenge, it was met. If there was a deadline, it was met.

It’s time for an official thank you.
We appreciate our relationship with GFR. From QC to communications, we have found working with GFR to be a pleasure, highlighted by excellent communications and reliable delivery dates. Thank you.
Michael BentleySierraSil Health Inc.